外科病理学 第5版

出版社: 文光堂
著者:
発行日: 2020-04-29
分野: 基礎医学  >  病理学
ISBN: 9784830604812
電子書籍版: 2020-04-13 (第5版第2刷)
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1984年刊行の初版より病理医に絶大なる支持を得ている『外科病理学』,14年ぶりの第5版改訂.「実用性を重視した病理診断医の座右の書」という初版からのコンセプトを守りつつ,現在の病理診断の標準を示すべくWHO分類,取扱い規約などに沿って最新の内容にアップデート.また,第4版まではモノクロ印刷であったのをフルカラー印刷とし,病理写真をカラー掲載した.病理専門医資格取得のためにも役立つ,すべての病理診断医にとって必携のテキスト.

目次

  • 〈第I巻〉
    1 イントロダクション
    2 皮膚・爪─非腫瘍性疾患─
    3 皮膚・爪─腫瘍性疾患─
    4 口腔・顎
    5 唾液腺
    6 上気道・耳・頸部
    7 肺─非腫瘍性疾患─
    8 肺・胸膜の腫瘍
    9 縦 隔
    10 食 道
    11 胃
    12 腸管─非腫瘍性疾患─
    13 腸管─腫瘍性疾患─
    14 肝
    15 胆囊・胆管・十二指腸乳頭部
    16 膵
    17 下垂体
    18 甲状腺
    19 副甲状腺
    20 副腎・傍神経節

    〈第II巻〉
    21 腎─非腫瘍性疾患─
    22 腎─腫瘍性疾患─
    23 尿路・男性外陰部
    24 精巣・付属器
    25 前立腺・精囊
    26 女性外陰部・腟・子宮頸部
    27 子宮体部
    28 卵巣・卵管
    29 胎盤
    30 乳腺
    31 リンパ節─非腫瘍性疾患─
    32 リンパ節─腫瘍性疾患─
    33 脾
    34 血液・骨髄
    35 末梢神経・骨格筋
    36 骨・関節
    37 軟部組織
    38 腹膜・後腹膜
    39 心臓
    40 血管
    41 中枢神経
    42 眼と眼付属器

この書籍の参考文献

参考文献のリンクは、リンク先の都合等により正しく表示されない場合がありますので、あらかじめご了承下さい。

本参考文献は電子書籍掲載内容を元にしております。

1 イントロダクション

P.11 掲載の参考文献
1) 深山正久 : 外科病理学の過去, 現在, そして近未来. 外科病理マニュアル, 病理と臨床 2008, 26 (臨増) : 2-10
2) 深山正久, 金井弥栄, 田中伸哉 (編) : 癌の分子病理学-病理診断から治療標的探索まで, 病理と臨床 2016, 34 (臨増)
6) 深山正久 : 目指せ, 病理医! 病理と臨床 2019, 37 : 10-16
7) 真鍋俊明, 三上芳喜 : 外科病理 (診断病理) の発展. 日本病理学会100周年記念誌, 日本病理学会, 2011, 43-52
8) 真鍋俊明 : 国立大学病院病理部会議 : 日本の外科病理学発展史の中での位置づけ. 国立大学病院病理部会議のあゆみ, 国立大学病院病理部会議, 2013, 6-15
9) 日本病理学会 : 病理専門医専攻医マニュアル 2019/01/11改訂版, 2019
10) 日本病理学会 (編) : 病理検体取り扱いマニュアル-病理検体取り違えを防ぐために-, 2016 http://pathology.or.jp/news/pdf/manual_all_160719.pdf
16) 日本病理学会 (編) : ゲノム診療用病理組織検体取扱い規程. 2018 http://pathology.or.jp/genome_med/pdf/textbook.pdf
24) https://ai.googleblog.com/2018/04/an-augmented-reality-microscope.html

2 皮膚・爪 - 非腫瘍性疾患 -

P.60 掲載の参考文献
1) 真鍋俊明, 幸田衛 : 皮膚病理診断アトラス-組織像の見方と臨床像, 文光堂, 1993, 2-49
2) 真鍋俊明, 清水道生 (編) : 皮膚腫瘍 I 角化細胞性腫瘍, 付属器系腫瘍と皮膚特有の間葉系腫瘍, 文光堂, 2010, 2-9
3) 清水宏 : あたらしい皮膚科学, 第3版, 中山書店, 2018, 1-38, 64-77
4) Mills SE : Histology for Pathologists, 5th ed, Wolters Kluwer, 2020, 3-30
5) Calonje E : McKee's Pathology of the Skin, 5th ed, Elsevier, 2020, 1-34
6) 清水道生 : 皮膚. 小田義直, 坂元亨宇, 深山正久 (編) : 組織病理アトラス, 第6版, 文光堂, 2015, 314-315
7) 清水道生, 小川史洋 : 皮膚炎症性疾患における組織反応パターン. 病理と臨床 2005, 23 : 702-708
26) Helander SD, De Castro FR, Gibson LE : Henoch-Schonlein purpura : clinicopathologic correlation of cutaneous vascular IgA deposits and the relationship to leukocytoclastic vasculitis. Acta Derm Venereol 1995, 75 : 125-129
29) Arya SR, Valand AG, Krishna K : A clinico-pathological study of 70 cases of pemphigus. Indian J Dermatol Venereol Leprol 1999, 65 : 168-171
32) Patel VM, Rubins S, Schwartz RA et al : Hailey-Hailey disease : a diagnostic challenge. Cutis 2019, 103 : 157-159
33) Wright JT, Fine JD : Hereditary epidermolysis bullosa. Semin Dermatol 1994, 13 : 102-107
48) Podder I, Dasm A : Non-bullous congenital ichthyosiform erythroderma. Indian Pediatr 2014, 51 : 679-680
62) 泉美貴 : 全身性エリテマトーデス. みき先生とゆう子先生の皮膚病理診断ABC 4, 炎症性病変, 学研メディカル秀潤社, 2013, 68-69
65) 泉美貴 : 関節リウマチの皮膚腫瘍病変 : 病理組織学的特徴による位置づけ. みき先生とゆう子先生の皮膚病理診断ABC 4, 炎症性病変, 学研メディカル秀潤社, 2013, 165
66) Huizenga T, Mehregan DR, Mehregan DA et al : Interstitial granulomatous dermatitis and palisaded neutrophilic granulomatous dermatitis. Cutis 2018, 101 : E19-E21
67) 泉美貴 : リウマトイド結節. みき先生とゆう子先生の皮膚病理診断ABC 4, 炎症性病変, 学研メディカル秀潤社, 2013, 132-133
68) 三上芳喜 : 病理組織形態のパターン認識. 真鍋俊明, 三上芳喜 (編) : 外科病理診断学原理とプラクティス, 金芳堂, 2018, 31-37, 56-61
69) 真鍋俊明 (監) : パターンの組織病理学. 外科病理診断学, 金芳堂, 1998, 17-23d
70) 真鍋俊明 : 炎症 1. "目からウロコ"の病理学総論, 金芳堂, 2018, 116-123
74) 泉美貴 : リポイド類壊死. みき先生とゆう子先生の皮膚病理診断ABC 4, 炎症性病変, 学研メディカル秀潤社, 2013, 130-131
75) 大塚藤男 : 性病・性感染症. 皮膚科学, 第10版, 金芳堂, 2016, 917-927
78) 真鍋俊明 : 組織標本でわかる感染性病原微生物と見えない場合に感染症を推測させる所見. 真鍋俊明, 安齋眞一, 宮地良樹 (編) : 皮膚病理の全て I, 文光堂, 2019, 412
79) 江川清文 : ヒトパピローマウイルスと皮膚疾患. ウイルス 2008, 58 : 173-182
80) 泉美貴 : 尋常性疣贅. みき先生の皮膚病理診断ABC 1, 表皮系病変, 秀潤社, 2006, 22-25
81) 江川清文 : 色素性疣贅 (くろいぼ) /ridged wart. 疣贅「いぼ」のみかた, 治療のしかた, 学研メディカル秀潤社, 2017, 84-91
82) Gonzales D, Manuel J, Luna M et al : Vestibular papillomatosis as a normal vulvar anatomical condition. Dermatol Online J 19 : 12 (https://escholarship.org/uc/item/2429w0sx 最終アクセス 2018年12月1日)
83) 三上芳喜 : 病原体. 真鍋俊明, 三上芳喜 (編) : 外科病理診断学原理とプラクティス, 金芳堂, 2018, 451-465
84) 清水宏 : 皮下脂肪組織疾患disorder of subcutaneous fat. 新しい皮膚科学, 第2版, 中山書店, 2011, 333-338
85) 真鍋俊明 : PANNICULITIS : SEPTAL PANNICULITIS. 真鍋俊明, 幸田衞 (編) : 皮膚病理診断アトラス組織像の見方と臨床像. 文光堂, 1993, 176-179
89) アミロイドーシスに関する調査研究班 : 全身性アミロイドーシス (指定難病28), http://www.nanbyou.or.jp/entry/207 (最終アクセス2018年12月1日)
90) John C, Maize SR, Ralston JS : Metabolic diseases of the skin. in : Elder DE,Elenitsas R, Rosenbach M et al (eds) : Lever's Histopathology of the Skin, 11th ed, 502-507
91) Olsen KE, Westermark P : Amyloid in basal cell carcinoma and seborrheic keratosis. Acta Derm Venereol 1994, 74 : 273-275
92) Began D. Dermatology Advisor, : Systemic Amyloidosis with Cutaneous Manifestations (Amyloidosis, Primary Systemic Amyloidosis, AL Amyloidosis (https://www.dermatologyadvisor.com/home/decision-support-in-medicine/dermatology/systemic-amyloidosis-with-cutaneous-manifestations-amyloidosis-primary-systemic-amyloidosis-al-amyloidosis/ (最終アクセス 2018年12月1日)
98) 泉美貴 : 皮膚および皮膚付属器. 赤木忠厚, 松原修, 真鍋俊明 (監) : カラーアトラス病理組織の見方と鑑別診断, 第6版, 医歯薬出版, 2018, 593
106) 大山学 : 脱毛症の病理組織検査の進め方-所見の解釈とそれに基づく治療とケア. MB Derma 2014, 225 : 23-29
107) 内山真樹 : 原発性瘢痕性脱毛症の最新のマネジメント. 日皮会誌 2019, 129 : 7-16
108) 川名誠司, 陳科榮 : 皮膚血管炎の概念, 分類および特徴. 皮膚血管炎, 医学書院, 2013, 15-26
110) 川名誠司 : 2012年Chapel Hill会議による血管炎の命名法を踏まえた新たな皮膚血管炎の命名法. 日皮会誌 2019, 129 : 23-38
111) Kawakami T, Soma Y, Mizoguchi M et al : Cutaneous Manifestations in Patients with Microscopic Polyangiitis : Two Case Reports and a Minireview. Acta Derm Venereol 2006, 86 : 144-147

3 皮膚・爪 - 腫瘍性疾患 -

P.132 掲載の参考文献
1) Elder DE, Massi D, Scolyer RA et al (eds) : WHO Classification of Skin Tumours, 4th ed, IARC Press, 2018
4) Cardoso JC, Caloonje E : Cutaneous manifestations of human papillomaviruses : a review. Acta Dermatovenerol Alp Pannonica Adriat 2011, 20 : 145-154
6) 新井栄一, 土田哲也 : 実践皮膚病理診断. 金原出版, 2017
26) Indinnimeo M, Impangnatiello A, D'Ettorre G et al : Buschke-Lowenstein tumor with squamous cell carcinoma treated with chemo-radiation therapy and local surgical excision : report of three cases. World J Surg Dermatol 2013, 41 : 241-243
36) Elder DE (editor-in-chief) : Lever's Histopathology of the Skin, 11th ed, Lipincott Williams and Wilkins, 2015
38) Khaled A, Kourda M, Fazaa B et al : Malignant proliferating trichilemmal cyst of the scalp : Histological aspects and nosology. Pathologica 2011, 103 : 73-76
41) 安齋眞一, 福本隆也, 木村鉄宣 : 脂腺母斑の臨床病理学的検討 : 第1報 年齢や発生部位と病理組織像の変化. 日皮会誌 2007, 117 : 1611-1620
42) 安齋眞一, 福本隆也, 木村鉄宣 : 脂腺母斑の臨床病理学的検討 : 第2報 二次性腫瘍について. 日皮会誌 2007, 117 : 2479-2487
44) Ackerman AB, Nussen-Lee S, Tan MA : Histopathologic Diagnosis of Neoplasms with Sebaceous Differentiation, Atlas and Text, 2nd ed, Ardor Scribendi, 2009
46) 安齋眞一, 木村鉄宣 : 脂腺腫 : sebaceoma 161例の臨床病理学的検討. 日皮会誌 2008, 118 : 2233-2241
47) 安齋眞一, 近藤慈夫 : 皮膚原発眼瞼外脂腺癌-自験15例の臨床病理学的検討. 日皮会誌 1999, 109 : 2111-2122
48) 安齋眞一, 木村鉄宣 : 脂腺癌 (sebaceous carcinoma) の臨床病理学的検討. 日皮会誌 2008, 118 : 2233-2241
51) 伊東慶悟, 安齋眞一, 木村鉄宣 : Poroid cell neoplasms. 421例の臨床病理学的検討. 第1報 : 4 組織亜型. 日皮会誌 2008, 118 : 2429-2434
53) 伊東慶悟, 安齋眞一, 木村鉄宣 : Poroid cell neoplasms. 421例の臨床病理学的検討. 第4報 : 病理組織学的随伴所見. 日皮会誌 2009, 119 : 173-182
54) Mascaro JM : Considerations sur les tumerus fibro-epitheliales : le syringofibroadenome eccrine. Ann Dermatol Syphiligr 1963, 90 : 146-153
57) 安齋眞一, 木村鉄宣, 真鍋求 : 皮膚混合腫瘍 (mixed tumor of the skin) の臨床病理学的検討. 日皮会誌 2007, 117 : 1959-1967
69) Clark WH Jr, Form L, Bermardino EA et al : The histogenesis and biologic behavior of primary human malignant melanomas of the skin. Cancer Res 1969, 29 : 705-727
73) Reed RJ, Ichinose H, Clark WH Jr et al : Common and uncommon melanocytic nevi and borderline melanomas. Semin Oncol 1975, 2 : 119-147
74) Smith NP : The pigmented spindle cell tumor of Reed : an underdiagnosed lesion. Semin Diagn Pathol 1987, 4 : 75-87
92) Swerdlow SH, Campo E, Harris NL et al (eds) : WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, Revised 4 th ed, IARC Press, 2017
114) Patel MD, Schleicher S : Cutaneous Metastasis from Renal Cell Carcinoma. Skinmed 2019, 17 : 65-66

4 口腔・顎

P.168 掲載の参考文献
1) El-Naggar AK, Chan JKC, Takata T et al (eds) : Odontogenic and maxillofacial bone tumours. WHO Classification of Head and Neck Tumours, 4th ed, IARC Press, 2017, 203-260
2) 小川郁子, 工藤保誠, 宮内睦美 他 : 外科病理マニュアル. 歯・顎骨. 病理と臨床 2008, 26 (臨増) : 139-143
3) 柳下寿郎, 出雲俊之 : 歯・顎骨. 森永正二郎, 高田隆, 長尾俊孝 (編) : 腫瘍病理鑑別診断アトラス 頭頸部腫瘍 II 上気道・咽頭・口腔腫瘍と歯原性腫瘍, 文光堂, 2015, 30-35
6) Ramer M, Valauri D : Multicystic lateral periodontal cyst and botryoid odontogenic cyst. Multifactorial analysis of previously unreported series and review of literature. N Y State Dent J 2005, 71 : 47-51
28) Said-Al-Naief N, Fernandes R, Louis P et al : Desmoplastic fibroma of the jaw : a case report and review of literature. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2006, 101 : 82-94
29) Tien N, Chaisuparat R, Fernandes R et al : Mesenchymal chondrosarcoma of the maxilla : case report and literature review. J Oral Maxillofac Surg 2007, 65 : 1260-1277
30) D'Silva NJ, Summerlin DJ, Cordell KG et al : Metastatic tumors in the jaws : a retrospective study of 114 cases. J Am Dent Assoc 2006, 137 : 1667-1672
31) Levaot N, Voytyuk O, Dimitriou I et al : Loss of tankyrase-mediated destruction of 3BP2 is the underlying pathogenic mechanism of cherubism. Cell 2011, 147 : 1324-1339
32) Triantafillidou K, Venetis G, Karakinaris G et al : Central giant cell granuloma of the jaws : a clinical study of 17 cases and a review of the literature. Ann Otol Rhinol Laryngol 2011, 120 : 167-174
33) Vered M, Carpenter WM, Buchner A et al : Granular cell tumor of the oral cavity : updated immunohistochemical profile. J Oral Patol Med 2009, 38 : 150-159
34) Yoshioka Y, Ogawa I, Tsunematsu T et al : Ectomesenchymal chondromyxoid tumor of the tongue : insights on histogenesis. Oral Surg Oral Med Oral Pathol Oral Radiol 2013, 115 : 233-240
35) Aldojain A, Jaradat J, Summersgill K et al : Ectomesenchymal chondromyxoid tumor : A series of seven cases and review of the literature. Head Neck Pathol 2015, 9 : 315-322
36) El-Naggar AK, Chan JKC, Takata T et al (eds) : Tumours of the oral cavity and mobile tongue. WHO Classification of Head and Neck Tumours, 4th ed, IARC Press, 2017, 106-131
37) The Working Committee for New Histopathological Criteria for Borderline Malignancies : Carcinoma in-situ of the oral mucosa : Its pathological diagnostic concept based on the recognition of histological varieties proposed in the JSOP Oral CIS Catalog. J Oral Maxillofac Surg Med and Pathol 2014, 26 : 397-406
38) Phlipsen HP, Reichart PA, Takata T et al : Verruciform xanthoma-biological profile of 282 oral lesions based on a literature survey with nine new cases from Japan. Oral Oncol 2003, 39 : 325-336
39) Lester SR, Cordell KG, Rosbush MS et al : Peripheral giant cell granuloma : a series of 279 cases. Oral Surg Oral Med Oral Pathol Oral Radiol 2014, 118 : 475-482
40) Vered M, Dobriyan A, Buchner A : Congenital granular cell epulis presents an immunohistochemical profile that distinguishes it from the granular cell tumor of the adult. Virchows Arch 2009, 454 : 303-310
41) American Academy of Periodontology : Informational paper. Drug-associated gingival enlargement. J Periodontol 2004, 75 : 1424-1431
42) 顎骨壊死検討委員会 : 骨吸収抑制薬関連顎骨壊死の病態と管理 : 顎骨壊死検討委員会ポジションペーパー 2016

5 唾液腺

P.215 掲載の参考文献
3) Harris NL : Lymphoid proliferations of the salivary glands. Am J Clin Pathol 1999, 111 (Suppl 1) : S94-S103
16) Kawahara A, Harada H, Abe H et al : Nuclear β-catenin expression in basal cell adenomas of salivary gland. J Oral Pathol Med 2011, 40 : 460-466
27) Nakaguro M, Urano M, Ogawa I et al : Histopathological evaluation of minor salivary gland papillary-cystic tumours : focus on genetic alterations in sialadenoma papilliferum and intraductal papillary mucinous neoplasm. Histopathology (in press)
28) 樋口佳代子・浦野誠 (監訳) : 唾液腺細胞診ミラノシステム, 金芳堂, 2019
43) Nakaguro M, Sato Y, Tada Y et al : Prognostic implication of histopathological indicators in salivary duct Carcinoma : proposal of a novel histologic risk stratification model. Am J Surg Pathol (in press)
52) Gupta A, Koochakzadeh S, Neskey DM et al : Salivary Carcinosarcoma : An Extremely Rare and Highly Aggressive Malignancy. Laryngoscope (in press)
53) Nagao T, Gaffey TA, Olsen KD et al : Small cell carcinoma of the major salivary gland : Clinicopathologic study with emphasis on cytokeratin 20 immunoreactivity and clinical outcome. Am J Surg Pathol 2004, 28 : 762-770
森永正二郎, 高田隆, 長尾俊孝 (編) : 腫瘍病理鑑別診断アトラス 頭頸部腫瘍 I 唾液腺腫瘍, 文光堂, 2015
青笹克之, 長尾俊孝, 高田隆 (編) : 唾液腺/口腔・歯原性腫瘍, 癌診療指針のための病理診断プラクティス, 中山書店, 2019
Wenig BM : Atlas of Head and Neck Pathology, 3rd ed, Elsevier, 2015
El-Naggar A, Chan JKC, Grandis JA et al (eds) : WHO Classification of Head and Neck Tumours, 4th ed, IARC Press, 2017
Wenig BM, Childers ELB, Richardson MS et al : Non-Neoplastic Diseases of the Head and Neck. Atlas of Non-Tumor Pathology, Series 1, Number 11, American Registry of Pathology, 2017
Thompson LDR, Bishop JA : Head and Neck Pathology, A volume in Foundations in Diagnostic Pathology, 3rd ed, Elsevier, 2019

6 上気道・耳・頸部

P.251 掲載の参考文献
1) Wenig BM : Atlas of Head and Neck Pathology. Elsevier, 2016
7) 湯淺博, 荻原仁, 藤田祐ほか : 鼻腔に生じた鼻硬化腫の1例. 診断病理 2018, 35 : 206-209
8) Wenig BM, Smirniotopoulos JG, Heffner DK : Botryomycosis ('bacterial ball') of the sinonasal tract caused by Pseudomonas aeruginosa. Arch Pathol Lab Med 1996, 120 : 1123-1128
21) El-Naggar AK, Chan JKC, Grandis JR et al (eds) : WHO Classification of Head and Neck Tumours, 4th ed, IARC Press, 2017
32) Chan JKC, Quintanilla-Martinez L, Ferry JA et al : Extranodal NK/T-cell lymphoma, nasal type. in : Swerdlow SH, Campo E, Harris NL et al (eds) : WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th ed, IARC Press, 2008, 285-288
35) Mills SE, Stelow EB, Hunt JL : Olfactory neuroblastoma. Tumors of the Upper Aerodigestive Tract and Ear, AFIP Atlas of Tumor Pathology, 4th series, ARP Press, 2012, 201-212
38) Mills ES, Stelow EB, Hunt JL : Metastatic neoplasms. Tumors of the Upper Aerodigestive Tract and Ear, AFIP Atlas of Tumor Pathology, 4th series, ARP Press, 2012, 465-468
54) Kontis TC, Goldstone A, Brown M et al : Pathologic quiz case 1. Auricular pseudocyst (benign idiopathic cystic chondromalacia, endochondral pseudocyst, or seroma of the auricle). Arch Otolaryngol Head Neck Surg 1992, 118 : 1128-1130
63) 飯塚栄 : 好エオジン球性リンパ腺炎およびリンパ肉芽腫症, 木村氏病の提唱. 日大医学雑誌 1959, 18 : 900-908
64) 木村啓二, 吉村三郎, 石川栄世 : リンパ組織増生変化を伴う異常肉芽腫に就いて, 特に他の類似変化の組織像との比較. 東京医事新誌 1948, 65 : 216-218
67) Damaskos C, Garmpis N, Manousi M et al : Cystic hygroma of the neck : single center experience and literature review. Eur Rev Med Pharmacol Sci 2017, 21 : 4918-4923

7 肺 - 非腫瘍性疾患 -

P.301 掲載の参考文献
1) Izumo T, Inomata M, Kuse N et al : Endobronchial Ultrasound and Cryobiopsy for Pulmonary Disease. JJSRE 2018, 40 : 505-510
3) Katzenstein A-LA : Diagnostic Atlas of Non-neoplastic Lung Disease : A Practical Guide for Surgical Pathologists, Demos Medical Publishing, 2016, 23-84
4) 長井苑子, 泉孝英 : びまん性肺疾患の臨床, 第4版, 金芳堂, 2012, 3-10
8) Amitani R, Niimi A, Kuze F : Idiopathic pulmonary upper lobe fibrosis (IPUF). Kokyu 1992, 11 : 693-699
10) Liebow AA, Carrington CB : The Interstitial Pneumonia (In Frontiers of Pulmonary Radiology) , Grune & Stratton, 1969, 102-141
15) Hunninghake GW, Fauci AS : Pulmonary involvement in the collagen vascular diseases. Am Rev Respir Dis 1979, 119 : 471-503
25) Leslie KO, Wick MR : Practical Pulmonary Pathology A Diagnostic Approach, Elsevier, 2018, 257-265
26) Katzenstein AL, Bloor CM, Leibow AA : Diffuse alveolar damage--the role of oxygen, shock, and related factors. A review. Am J Pathol 1976, 85 : 209-228
28) Davison AG, Heard BE, McAllister WA et al : Cryptogenic organizing pneumonitis. Q J Med 1983, 52 : 382-394
37) Cutz E : Idiopathic pulmonary hemosiderosis and related disorders in infancy and childhood. Perspect Pediatr Pathol 1987, 11 : 47-81
42) Moran CA, Hochholzer L, Hasleton PS et al : Pulmonary alveolar microlithiasis. A clinicopathologic and chemical analysis of seven cases. Arch Pathol Lab Med 1997, 121 : 607-611
51) Koss MN, Hochholzer L, Feigin DS et al : Necrotizing sarcoid-like granulomatosis : clinical, pathologic, and immunopathologic findings. Hum Pathol 1980, 11 : 510-519
55) 堤寛 : 輸入真菌症 I : ブラストミセス症, コクシジオイデス症, パラコクシジオイデス症. 感染症病理アトラス, 文光堂, 2000, 126-127
56) 堤寛 : フィラリア症, オンコセルカ症, 犬糸状虫症. 感染症病理アトラス, 文光堂, 2000, 244-246
58) Craighead J, Kleinerman J, Abraham JL : Diseases associated with exposure to silica and nonfibrous silicate minerals. Silicosis and Silicate Disease Committee. Arch Pathol Lab Med 1988, 112 : 673-720
67) Stocker JT : Sequestrations of the lung. Semin Diagn Pathol 1986, 3 : 106-121
71) Stocker JT : Congenital pulmonary airway malformation : A new name for and an expanded classification of congenital cystic adenomatoid malformation of the lung. Histopathol 2002, 41 : 424-430

8 肺・胸膜の腫瘍

P.373 掲載の参考文献
1) Mills SE (ed) : Histology for Pathologists, 4th ed, Lippincott Williams&Wilkins, 2012
2) 日本肺癌学会 (編) : 臨床・病理 肺癌取扱い規約, 第8版, 金原出版, 2017
3) 日本病理学会 ゲノム診療用病理組織検体取扱い規程策定ワーキンググループゲノム診療用病理組織検体取扱い規程, 日本病理学会, 2018 http://pathology.or.jp/genome_med/pdf/textbook.pdf.
4) 深山正久, 野口雅之, 松野吉宏 (編) : 腫瘍病理鑑別診断アトラス 肺癌, 文光堂, 2014
20) 橋本大輝, 元井紀子 : 肺癌の病理コンパニオン診断 update. 肺癌 2018, 58 : 77-82
24) 日本肺癌学会. 肺癌診療ガイドライン https://www.haigan.gr.jp/modules/guideline/index.php?content_id=33
25) Travis WD, Brambilla E, Noguchi M et al : International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society International Multidisciplinary Classification of Lung Adenocarcinoma. J Thorac Oncol 2011, 6 : 244-285
28) Travis W, Brambilla E, Burke AP et al (eds) : WHO Classification of Tumours of the Lung, Pleura, Thymus and Heart, 4th ed, IARC Press, 2015
29) 日本肺癌学会 (編) : 肺癌診療ガイドライン 2018年版 第5版 悪性胸膜中皮腫・胸腺腫瘍含む, 金原出版, 2018
30) Dail DH, Hammar SP (eds) : Dail and Hammar's Pulmonary Pathology, 3rd ed, Springer Science+Business Media, 2008
32) 厚生労働省「全国がん登録の概要」 https://www.mhlw.go.jp/content/10900000/000468976.pdf
33) 人口動態統計によるがん死亡データ https://ganjoho.jp/reg_stat/statistics/stat/summary.html
35) Fitzmaurice C, Allen C, Barber RM et al : Global, Regional, and National Cancer Incidence, Mortality, Years of Life Lost, Years Lived With Disability, and Disability-Adjusted Life-years for 32 Cancer Groups, 1990 to 2015 A Systematic Analysis for the Global Burden of Disease Study. JAMA Oncol 2017, 3 : 524-548
40) 東出直樹, 菊地利明, 一ノ瀬正和 : 家族性肺癌. 最新肺癌学-基礎と臨床の最新研究動向-, 日本臨床 2013, 71 (増刊 6) : 78-83
42) IARC Monographs on the Identification of Carcinogenic Hazards to Humans http://publications.iarc.fr/Book-And-Report-Series/Iarc-Monographs-On-The-Identification-Of-Carcinogenic-Hazards-To-Humans
45) Detterbeck FC, Franklin WA, Nicholson AG et al : The IASLC Lung Cancer Staging Project : Background Data and Proposed Criteria to Distinguish Separate Primary Lung Cancers from Metastatic Foci in Patients with Two Lung Tumors in the Forthcoming Eighth Edition of the TNM Classification for Lung Cancer. J Thorac Oncol 2016, 11 : 651-665
61) 中谷行雄, 太田聡 : 胎児型腺癌 低, 高悪性度. 深山正久, 野口雅之, 松野吉宏 (編) : 腫瘍病理鑑別診断アトラス 肺癌, 文光堂, 2014, 84-91
63) Zhang TM, Lu BH, Cai YR et al : Well-differentiated fetal adenocarcinoma of the lung : clinicopathologic features of 45 cases in China Int J Clin Exp Pathol 2018, 11 : 1587-1598
65) Matsushima J, Yazawa T, Suzuki M et al : Clinicopathological, immunohistochemical, and mutational analyses of pulmonary enteric adenocarcinoma : usefulness of SATB2 and β-catenin
71) 後藤悌, 元井紀子 : 肺・縦隔発生の神経内分泌腫瘍 : 病理診断と治療 Update. 肺癌 2019, 59 : 37-45
91) Yeh, Y., Ho, H., Wu, Y. et al : AKT1 internal tandem duplications and point mutations are the genetic hallmarks of sclerosing pneumocytoma. Mod Pathol 2019. https://doi.org/10.1038/s41379-019-0357-y
93) 石川雄一 : 肺末梢の線毛性粘液結節性乳頭状腫瘍 : 良性か悪性か? 病理と臨床 2002, 20 : 964-965
114) 湊宏 : 肺転移性腫瘍の鑑別診断. 病理と臨床 2010, 28 : 239-251
116) 石綿・中皮腫研究会, 日本中皮腫研究機構, 日本肺癌学会 (編) : 中皮腫瘍取扱い規約, 金原出版, 2018
117) Nicholson AG, Sauter JL, Nowak AK et al : EURACAN/IASLC Proposals for Updating the Histologic Classification of Pleural Mesothelioma : Towards a More Multidisciplinary Approach. J Thorac Oncol 2020, 15 : 29-49
119) 亀井敏昭, 畠榮, 濱川真治ほか : 中皮腫診断での体腔液細胞診の意義. 病理と臨床 2019, 37 : 1110-1119

9 縦隔

P.409 掲載の参考文献
4) Perez-Ordonez B, Wesson DE, Smith CR et al : A pancreatic cyst of the anterior mediastinum. Mod Pathol 1996, 9 : 210-214
6) 中智昭, 外丸詩野, 松野吉宏 : 胸腺. 病理診断に直結した組織学, 病理と臨床 2017, 35 (臨増) : 151-160
9) Tomaru U, Tsuji T, Kiuchi S et al : Decreased expression of thymus-specific proteasome subunit β5t in Down syndrome patients. Histopathology 2015, 67 : 235-244
12) Strobel P, Marx A, Badve S et al : Type A thymoma, including atypical variant. in Travis WD, Brambilla E, Buirke AP et al (eds) : WHO Classification of Tumours of the Lung, Pleura, Thymus, and Heart, 4th ed, IARC Press, 2015, 187
15) 特定非営利活動法人日本肺癌学会 : 第3部 胸腺腫瘍診療ガイドライン 2018年版 I. 診断 3. 確定診断. 肺癌診療ガイドライン 2018年版 悪性胸膜中皮腫・胸腺腫瘍含む, 第5版, 金原出版, 2018, 333-335
18) Chan JKC, Strobel P, Marx A et al : Squamous cell carcinoma. in Travis WD, Brambilla E, Buirke AP et al (eds) : WHO Classification of Tumours of the Lung, Pleura, Thymus, and Heart, 4th ed, IARC Press, 2015, 212
19) Strobel P, Marx A, Chan JKC et al : Thymic neuroendocrine tumours : Typical and atypical carcinoid. in Travis WD, Brambilla E, Buirke AP et al (eds) : WHO Classification of Tumours of the Lung, Pleura, Thymus, and Heart, 4th ed, IARC Press, 2015, 234
24) Moreira AL, Chan JKC, Looijenga LHJ et al : Seminoma. in Travis WD, Brambilla E, Buirke AP et al (eds) : WHO Classification of Tumours of the Lung, Pleura, Thymus, and Heart, 4th ed, IARC Press, 2015, 244

10 食道

P.440 掲載の参考文献
2) 石黒信吾 : 食道. 向井清, 真鍋俊明, 深山正久 (編) : 外科病理学, 第4版, 文光堂, 2006, 400
6) 大橋健一, 立石陽子 : 食道生検診断の現状と問題点. 病理と臨床 2016, 34 : 909-914
8) 木下芳一, 大嶋直樹, 石村典久ほか : 好酸球性消化管障害の診断と治療. 日消誌 2013, 110 : 953-964
9) Wagtmann MJ, Verspaget HW, Lamers CB et al : Clinical aspects of Crohn's disease of the upper gastrointestinal tract : a comparison with distal Crohn's disease. Am J Gastroenterol 1997, 92 : 1467-1471
14) 新田宙, 山下純男, 伊藤博ほか : 巨大な食道fibrovascular polyp の1例. 日臨外会誌 2007, 68 : 839-844
15) 大倉康男 : 生検標本における食道扁平上皮dysplasiaの病理組織診断. 胃と腸 2007, 42 : 137-145
16) 相田順子, 新井冨生, 櫻井うららほか : 食道炎, 異型上皮, 扁平上皮癌の鑑別診断. 病理と臨床 2011, 29 : 926-931
23) Bosman FT, Carneiro F, Hruban RH et al (eds) : WHO Classification of Tumors of the Digestive System, 4th ed, IARC Press, 2010
24) 藤井誠志 : 扁平上皮癌の悪性度評価. 田久保海誉, 大橋健一 (編) : 腫瘍病理鑑別診断アトラス 食道癌, 文光堂, 2012, 103-108
27) 渡辺玄, 味岡洋一 : 炎症に伴う再生異型と上皮内腫瘍の鑑別診断. 腫瘍病理鑑別診断アトラス 食道癌, 文光堂, 2012, 170-174
28) 河内洋, 小林真季, 小池盛雄ほか : 食道上皮内腫瘍性病変の組織像と遺伝子異常. 胃と腸 2007, 42 : 173-186
32) 渡辺英伸, 田邊 匡, 八木一芳ほか : 食道胃接合部癌の病理学的特徴-組織発生の面からBarrett食道癌と比較して. 胃と腸 2001, 36 : 634-645
33) 大橋健一 : 食道胃接合部に発生する早期腺癌の病理形態像について. 病理と臨床 2003, 22 : 563-568
38) 大橋健一 : 食道原発の類基底細胞癌について. 病理と臨床 2002, 20 : 471-478
39) 大橋健一 : 類基底細胞癌と基底膜様物質. 病理形態学キーワード, 病理と臨床 2010, 28 (臨増) : 104-105
43) Fenoglio-Preiser CM, Noffsinger AE, Sremmermann GN et al : Gastrointestinal Pathology, 3rd ed, Wolters Kluwer/Lippincott Williams & Wilkins, 2008, 107-109
44) 日本食道学会全国登録委員会 : Complehensive registry of esophageal cancer in Japan 1988-1999. 日本食道学会ホームページ (http://esophagus.jp)
46) 大倉康男 : 食道原発癌肉腫の臨床と病理. 病理と臨床 2002, 20 : 489-495
47) 新井冨生, 相田順子, 馬場聡ほか : 平滑筋腫瘍, GIST, 神経性腫瘍, 血管腫瘍. 田久保海誉, 大橋健一 (編) : 腫瘍病理鑑別診断アトラス 食道癌, 文光堂, 2012, 145-153

11 胃

P.509 掲載の参考文献
1) 内山安男, 相磯貞和 (監訳) : 食道, 胃と腸. Ross組織学 (Michael H. Ross), 原著第5版, 南江堂, 2010, 518-575
2) 日本胃癌学会 (編) : 胃癌取扱い規約, 第15版, 金原出版, 2017
3) 八木一芳, 味岡洋一 : 胃の拡大内視鏡診断, 医学書院, 2012, 7
4) 向所賢一, 九嶋亮治 : 胃. 病理診断に直結した組織学, 病理と臨床 2017, 35 (臨増) : 189-201
5) Owen DA : Stomach. Stacey EM (ed) : Histology for Pathologists, 4th ed, Wolters Kluwer/Lippincott Williams & Wilkins, 2012, 633-646
6) 二村聡, 塩飽洋生, 山下兼史ほか : 胃癌の切除標本診断. 臨消内科 2015, 30 : 834-841
7) 二村聡 : 切除標本の取り扱いとマクロ写真撮影-消化管画像診断に必要な病理標本の取り扱いの基本手順. 胃と腸 2016, 51 : 1176-1184
8) 二村聡, 梅垣英次 : 内視鏡切除標本の取扱いと根治度評価. 日本消化器内視鏡学会卒後教育委員会 (編) : 消化器内視鏡ハンドブック, 改訂第2版, 日本メディカルセンター, 2017, 291-299
15) 岩下明徳 : 過誤腫. 胃と腸 2017, 52 : 699-700
16) 滝澤登一郎 : 胃の病理形態学, 医学書院, 2006
25) 加藤元嗣, 井上和彦, 村上和成ほか (編) : 胃炎の京都分類, 日本メディカルセンター, 2018, 136-138
26) 九嶋亮治 : 胃炎の京都分類と京都国際胃炎コンセンサス会議. 病理と臨床 2015, 33 : 1026-1029
29) 丸山保彦, 景岡正信, 大畠朗彦ほか : A型胃炎の診断. 胃と腸 2016, 51 : 77-86
35) Coffey RJ Jr, Tanksley J : Pierre Menetrier and his disease. Trans Am Clin Climatol Assoc 2012, 123 : 126-133
38) Kawasaki M, Hizawa K, Aoyagi K et al : Menetrier's disease associated with Helicobacter pylori infection : resolution of enlarged gastric folds and hypoproteinemia after antibacterial treatment. Am J Gastroenterol 1997, 92 : 1909-1912
41) 中原束 : スキルス胃癌と鑑別を要する非腫瘍性疾患-サルコイドーシス. 胃と腸 2010, 45 : 515-520
45) Kushima R, Borchard F : Lymphocytic gastritis : autoimmune disease or variant of Helicobacter gastritis? Verh Dtsch Ges Pathol 1996, 80 : 208-211
53) 九嶋亮治 : Helicobacter heilmannii胃炎の病理診断. 病理と臨床 2017, 35 : 961-963
55) Atten MJ, Attar BM, Teopengco E et al : Gastric syphilis : a disease with multiple manifestations. Am J Gastroenterol 1994, 89 : 2227-2229
66) 菅野武, 飯島克則, 小池智幸ほか : 非H. pylori・非薬剤性胃潰瘍. 胃と腸 2017, 52 : 900-906
67) 崎田隆夫, 福富久之 : 胃潰瘍の診断. 吉利和 (編) : 胃・十二指腸潰瘍のすべて, 南江堂, 1971, 197-208
68) 村上忠重, 鈴木武松 : 病理. 吉利和 (編) : 胃・十二指腸潰瘍のすべて, 南江堂, 1971, 79-102
72) The WHO Classification Tumours Editorial Boards (ed) : WHO Classification of Tumours : Digestive System Tumors, 5th ed, IARC Press, 2019
85) 森源喜, 小田一郎, 谷口浩和ほか : 胃腺腫に対する治療方針私はこう思う : 経過観察する立場から. 胃と腸 2014, 49 : 1859-1869
87) 九嶋亮治, 松原亜季子, 吉永繁高ほか : 胃型腺腫の臨床病理学的特徴-内視鏡像, 組織発生, 遺伝子変異と癌化. 胃と腸 2014, 49 : 1838-1849
95) Schlemper RJ, Riddell RH, Kato Y et al : The Vienna classification of gastrointestinal epithelial neoplasia. Gut 2000, 47 : 251-255
97) 九嶋亮治 : 胃の腺窩上皮とラズベリー様ポリープ. 病理と臨床 2019, 37 : 1024-1027
99) Sugano H, Nakamura K, Kato Y : Pathological studies of human gastric cancer. Acta Pathol Jpn 1982, 329-347
113) Kinjo T, Taniguchi H, Kushima R : Histologic and immunohistochemical analyses of α-fetoprotein producing cancer of the stomach. Am J Surg Pathol 2012, 36 : 56-65
123) Mori M, Iwashita A, Enjoji M : Squamous cell carcinoma of the stomach : report of three cases. Am J Gastroenterol 1986, 81 : 339-342
125) 前田将宏, 谷口浩和, 関根茂樹ほか : 胃腺扁平上皮癌の臨床病理学的研究. 胃と腸 2010, 45 : 1959-1966
141) Swerdlow SH, Campo E, Harris NC et al (eds) : WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th ed, Revised ed, IARC Press, 2017
142) 佐野量造 : 胃疾患の臨床病理, 医学書院, 1974
143) 八尾恒良, 中沢三郎, 中村恭一ほか : 胃悪性リンパ腫の集計成績. 胃と腸 1980, 15 : 906-908
144) 二村聡 : 消化管リンパ腫の病理診断-基本的事項を中心に. 胃と腸 2014, 49 : 574-580
150) 竹下盛重, 二村聡, 菊間幹太ほか : 成人T細胞白血病/リンパ腫を含む消化管T/NK細胞リンパ腫の臨床病理学的特徴-リンパ腫の細胞起源についての考察を含む. 胃と腸 2014, 49 : 769-781
153) 原季衣, 小上暎也, 海崎泰治 : Lymphomatoid gastropathyの1例. 診断病理 2018, 35 : 85-89
163) 日本癌治療学会, 日本胃癌学会, GIST研究会 (編) : GIST診療ガイドライン, 第3版, 金原出版, 2014
164) 南部匠, 渡辺英伸, 遠城寺宗知 : 胃のinflammatory fibroid polyp-特にその初期病変について. 福岡医誌 1979, 70 : 721-731
165) Schildhaus HU, Cavlar T, Binot E et al : Inflammatory fibroid polyps harbour mutations in the platelet-derived growth factor receptor alpha (PDGFRA) gene. J Pathol 2008, 216 : 176-182

12 腸管 - 非腫瘍性疾患 -

P.560 掲載の参考文献
1) Katzin WE, Petras RE : Small intestine. in Milles SE (ed) : Histology for Pathologists, 4th ed, Lippincott Williams & Wilkins, 2012, 647-671
2) Dahl J, Greenson JK : Colon. in Milles SE (ed) : Histology for Pathologists, 4th ed, Lippincott Williams & Wilkins, 2012, 673-695
3) Katzin WE, Petras RE : Vermiform appendix. in Milles SE (ed) : Histology for Pathologists, 4th ed, Lippincott Williams & Wilkins, 2012, 697-708
4) Fenger C : Anal canal. in Milles SE (ed) : Histology for Pathologists, 4th ed, Lippincott Williams & Wilkins, 2012, 709-731
5) Noffsinger AE, Amy E : Fenoglio-Preiser's Gastrointestinal Pathology, 4th ed, Wolters Kluwer, 2017
6) Shepherd NA, Warren BF, Williams GT et al : Morson and Dawson's Gastrointestinal Pathology, 5th ed, Wiley-Blackwell, 2013, 281-410, 477-489, 511-646
7) 岩下明徳 : 小腸・虫垂・大腸・肛門 : 非腫瘍性病変. 向井清, 真鍋俊明, 深山正久 (編) : 外科病理学, 第4版, 文光堂, 2006, 503-559
8) Noffsinger AE, Fenoglio-Preiser CM, Maru D et al : Gastrointestinal Diseases. American Registry of Pathology, Washington, 2007
9) 中崎久雄, 森屋秀樹, 太田正敏ほか. 大腸壁在神経叢の脱落によるSegmental aganglionosisの2症例. 日本大腸肛門病会誌 1997, 50 : 45-52
18) Louw JH : Congenital intestinal atresia and stenosis in the newborn. Observations or its pathogenesis and treatment. Ann R Coll Surg 1959, 25 : 209-234
19) Santulli TV, Blanc WA : Congenital atresia of the intestine. Pathogenesis and treatment. Ann Surg 1961, 154 : 939-948
20) 川崎茂喜 : 先天性上部小腸閉鎖症の臨床的ならびに病理組織学的研究. 日臨外会誌 1972, 33 : 15-35
22) Gross RE : Duplications of the alimentary tract. in Gross RE (ed) : The Surgery of Infancy and Childhood, WB Saunders, 1952, 221-245
24) Soderlund S : Meckel's diverticulum ; A clinical and histologic study. Acta Chir Scand 1959, 248 (Suppl) : 1-233
27) 須崎真, 三田正明, 岩崎誠他 : Intraluminal duodenal diverticulum の1例. 胃と腸 1983, 18 : 273-277
28) 井上幹夫, 吉田一郎, 久保明良ほか : わが国における大腸憩室症 (大腸憩室疾患) の実態. 胃と腸 1980, 15 : 807-815
30) 石川信, 加藤順 : 大腸憩室疾患-日本における最近の傾向. 日本大腸肛門病会誌 2008, 61 : 1010-1014
33) 田口智章班・Hirschsprung 病類縁疾患グループ : 小児期からの希少難治性消化管疾患の移行期を包含するガイドラインの確立に関する研究 : 平成27年度総括・分担研究報告書 : 厚生労働科学研究費補助金難治性疾患等政策研究事業 (難治性疾患政策研究事業), 田口智章班, 2017
34) 多田修治, 飯田三雄. 原発性, 続発性アミロイドーシス. 胃と腸 2003, 38 : 611-618
35) 小林正明, 森田俊, 宮崎滋ほか : 透析アミロイドーシス. 胃と腸 2003, 38 : 619-627
36) 藤澤律子, 松本主之, 中村昌太郎ほか : 腸管嚢胞様気腫症. 胃と腸 2005, 40 : 657-660
38) Yamaguchi K, Shirai T, Shimakura K et al : Pneumatosis cystoides intestinalis and trichloroethylene exposure. Am J Gastroent 1985, 80 : 753-757
41) Walker NI, Bannett RE, Axelse RA : Melanosis coli. A consequence of anthraquinone-induced apoptosis of colonic epithelial cells. Am J Pathol 1988, 131 : 465-476
45) 中澤英之, 牧島秀樹, 石田文宏ほか : セリアック病. 胃と腸 2008, 43 : 651-655
46) 長末智寛, 蔵原晃一, 川崎啓祐ほか : Whipple病の特徴. Intestine 2017, 21 : 554-558
48) 中村志郎, 野上孝司, 樋田信幸ほか : タキサン系抗癌剤による虚血性大腸炎の2例. 胃と腸 2013, 48 : 1785-1790
50) 八尾隆史, 蔵原晃一, 大城由美ほか : 非ステロイド系抗炎症例 (NSAID) 起因性腸病変の臨床病理学的特徴と病態. 胃と腸 2007, 42 : 1691-1700
54) 林繁和, 神部隆吉, 家田秀明ほか : 抗生物質起因性腸炎の臨床像と鑑別診断. 胃と腸 2000, 35 : 1125-1134
55) Boley SJ, Schwartz S, Lash J et al : Reversible vascular occlusion of the colon. Surg Gynec Obstet 1963, 116 : 53-60
57) Marston A : Intestinal Ischaemia, Edward Arnold, 1977, 71-83, 132-138, 143-150
58) 岩下明徳, 住吉金次郎, 桜井剛ほか : 虚血性大腸炎-組織像からみた成因について. 病理と臨床 1984, 2 : 193-206
59) 岩下明徳, 八尾隆史, 飯田三雄ほか : 虚血性小腸狭窄 (狭窄型虚血性小腸炎) の臨床病理学的検索. 胃と腸 1990, 25 : 557-569
60) 岩下明徳, 竹村聡, 山田豊ほか : 原因別にみた虚血性腸病変の病理形態. 胃と腸 1993, 28 : 927-941
61) 黒岩重和, 八尾隆史, 岩下明徳 : 結節性動脈周囲炎における腸潰瘍の病理学的特徴. 胃と腸 1991, 26 : 1257-1265
62) 松本啓志, 村尾高久, 葉祥元ほか : 血管炎による消化管病変の臨床診断. 結節性多発動脈炎. 胃と腸 2015, 50 : 1389-1396
63) 柿本一城, 村野実之, 井上拓也ほか : 血管炎による消化管病変の臨床診断. 顕微鏡的多発血管炎と多発血管炎性肉芽腫症 (Wegener肉芽腫症). 胃と腸 2015, 50 : 1381-1387
64) 江崎幹宏, 梅野淳嗣, 前畠裕司ほか : 血管炎による消化管病変の臨床診断. IgA血管炎 (Schonlein-Henoch紫斑病). 胃と腸 2015, 50 : 1363-1371
65) 小林広幸, 渕上忠彦, 西木茂ほか : 慢性関節リウマチ患者にみられた腸の潰瘍性病変. 胃と腸 1991, 26 : 1247-1256
74) 吉永繁高, 中村和彦, 原田直彦ほか : 特発性腸間膜 静脈硬化症の臨床-臨床像. 胃と腸 2009, 44 : 163-169
75) 大津健聖, 松井敏幸, 西村拓ほか : 漢方薬内服により発症した腸間膜静脈硬化症の臨床経過. 日消誌 2014, 111 : 61-68
76) 池田圭祐, 岩下明徳, 田邉寛ほか : 血管炎による消化管病変の病理診断. 胃と腸 2015, 50 : 1353-1362
77) 小山登, 小山洋, 花島得三ほか : 慢性的経過を呈した右側狭窄型虚血性大腸炎の1例. 胃と腸 1991, 26 : 455-460
78) 帆足俊男, 前田和弘, 松井敏幸ほか : 著明な静脈の石灰化を伴った静脈硬化症による虚血性腸病変の1例. 胃と腸 1993, 28 : 967-973
79) 住吉金次郎 : 閉塞性大腸炎の臨床病理学的研究. 福岡医誌 1988, 79 : 749-766
80) 青山浩幸, 丸太守人, 前田耕太郎 : 閉塞性大腸炎の病態と診断・治療. 臨外 1999, 54 : 1567-1571
81) 市原利晃, 天満和男, 南条博ほか : 閉塞性大腸炎の検討. 日消外科誌 2002, 35 : 673-677
82) 小嶋伸夫, 富永雅也, 岡部信彦ほか : 大腸に多発潰瘍を認めた腸チフスの1例. 胃と腸 1992, 27 : 1451-1456
83) 富永雅也, 廣田千治, 徳永剛ほか : 全結腸にびまん性に潰瘍の多発をみたサルモネラ腸炎の1例. 胃と腸 1992, 27 : 1329-1336
85) 清水誠治, 木本邦彦, 多田正大 : キャンピロバクター腸炎. 胃と腸 2002, 37 : 347-351
86) 山崎節, 小川清, 坪田順昭ほか : Yersinia enterocoliticaによる急性回腸末端炎の2例. 胃と腸 1983, 18 : 399-406
88) 渡辺英伸, 遠城寺宗知, 八尾恒良 : 腸結核の病理. 胃と腸 1977, 12 : 1481-1496
89) 小林広幸 : 本邦における消化管結核の現況. 近年の本邦報告例の解析. 胃と腸 2017, 52 : 145-156
91) 松井佐織, 吉田晋也, 野口千彰ほか : 最近注目される腸管感染症. クラミジア直腸炎. 胃と腸 2018, 53 : 441-445
92) 立石陽子, 堀口慎一郎, 根本哲生ほか : 腸管スピロヘータの感染頻度と臨床病理学的検討. 診断病理 2010, 27 : 189-192
93) 田邉寛, 岩下明徳, 原岡誠司ほか : 腸管スピロヘータ症-自験34例からみた内視鏡像・臨床的意義・治療. 胃と腸 2008, 43 : 1670-1679
94) 杉田光司, 片岡伸一, 西岡伸明ほか : 腸管スピロヘータが原因と考えられた大腸炎の1例. Gastroenterol, Endosc 2012, 54 : 3596-3600
95) 北野厚生, 松本誉之, 押谷伸英ほか : アメーバ赤痢. 胃と腸 1997, 32 : 481-487
96) 金城福則, 内間康文, 座間修ほか : 非腫瘍性びまん性十二指腸病変の診断-糞線虫症のX線, 内視鏡所見を中心に. 胃と腸 2002, 37 : 819-828
97) 松本主之, 檜沢一興, 浅野光一ほか : ランブル鞭毛虫症. 胃と腸 2002, 37 : 405-408
98) 九嶋亮治, 茂籠邦彦, 角谷亜紀ほか : 小腸生検にて診断しえた戦争イソスポーラ感染症の1例. 診断病理 2003, 20 : 360-362
99) 池田圭祐, 岩下明徳, 田邉寛ほか : 組織像でわかる感染性腸炎. 胃と腸 2008, 43 : 1590-1605
100) 寺田紘一-近藤慶二-上仁ほか : 本邦報告例からみた腸型ベーチェット切除75例の臨床. 外科 1983, 45 : 1421-1429
101) 長尾孝一, 松嵜理, 更科広美ほか : Intestinal Behcet病の病理組織学的解析. 大腸肛門誌 1976, 29 : 409-419
102) 渡辺 勇, 岡田基, 桑原紀之ほか : 腸管型Behcet病といわゆるSimple ulcer-組織学的診断における問題点. 病理と臨床 1984, 2 : 233-244
103) 武藤徹一郎 : いわゆる "Simple ulcer" とは. 胃と腸 1979, 14 : 739-748
104) 北陸平, 中村積方, 松島康博ほか : 回盲部単純性非特異性潰瘍-自験2例と本邦報告81例の検討-. 消化器外科 1985, 8 : 111-120
105) 渡辺英伸 : 非腫瘍性腸疾患の病理. 病理と臨床 1984, 2 : 1219-1230
106) 多田正大, 傍島淳子, 清水誠治ほか : 腸管Behcet病とsimple ulcerの臨床経過-疾病史からみた腸型Behcet病とsimple ulcerの異同. 胃と腸 1992, 27 : 313-318
108) 池田圭祐, 岩下明徳 : 大腸炎症性疾患の病理診断-肉芽腫の鑑別を中心に-. 病理と臨床 2008, 26 : 795-802
110) 渡辺英伸, 味岡洋一, 西倉健 : 潰瘍性大腸炎-病理診断. 胃と腸 1997, 32 : 309-316
112) 味岡洋一, 渡辺英伸, 小林正明ほか : 潰瘍性大腸炎に合併する大腸癌・dysplasia の肉眼実体顕微鏡像と生検組織診断. 胃と腸 1995, 30 : 629-642
113) Dalziel TK : Chronic interstitial enteritis. Br Med J 1913, ii : 1068-1070
118) 斎藤建, 高橋敦, 町田武久ほか : クローン病の病理組織学的診断. 胃と腸 1975, 10 : 1053-1061
119) 渡辺英伸, 遠城寺宗知, 八尾恒良 : クローン病の病理. 胃と腸 1978, 13 : 351-373
120) 山形敞一, 馬場正三, 細田四郎ほか : クローン病診断基準 (案). 日消誌 1976, 73 : 1467-1478
121) 岩下明徳, 八尾恒良, 渡辺英伸ほか : 術前の治療法別にみたCrohn病の病理形態像. 胃と腸 1984, 19 : 287-308
122) 武藤徹一郎 : Crohn病診断基準 (案). 胃と腸 1996, 31 : 449-450
123) 八尾恒良 : 新しいCrohn病の診断基準 (案) について. 胃と腸 1996, 31 : 451-464
124) 岩下明徳, 山田豊, 喜多村邦弘ほか : Crohn病-病理診断. 胃と腸 1997, 32 : 365-376
127) 渡辺英伸, 味岡洋一, 田口夕美子ほか : 直腸の粘膜脱症候群 (mucosal prolapse syndrome) の病理形態学的検討. 胃と腸 1987, 22 : 303-312
128) 太田玉紀, 味岡洋一, 渡辺英伸 : 直腸の粘膜脱症候群, 病理の立場から. 胃と腸 1990, 25 : 1301-1311
129) Ohta T : Mucosal prolapse syndrome of the rectum : Correlation between macroscopic type and location in a discussion on its natural history. Acta Med Biol 1993, 41 : 33-43
130) Williams GT, Bussey HJR, Morson BC : Inflammatory 'cap' polyps of the large intestine. Br J Surg 1985, 72 (Suppl) : S133
132) 八尾隆史, 江崎幹宏, 古賀秀樹ほか : cap polyposisの臨床病理学的特徴. 粘膜脱症候群との比較. 胃と腸 2002, 3 : 631-639
133) 松本主之, 梅野淳嗣, 江崎幹宏ほか : 非特異性多発性小腸潰瘍症/CEASとプロスタグランジン腸症. 胃と腸 52 : 1406-1410, 2017.
134) 田邊寛, 岩下明徳. 非特異性多発性小腸潰瘍症/CEASの臨床病理学的特徴と鑑別疾患. 胃と腸 2017, 52 : 1431-1439
135) 岡部治弥, 崎村正弘, 岡山昌弘ほか : 非特異性原発性小腸潰瘍の3例. 日内会誌 1966, 55 : 215
136) 岡部治弥, 崎村正弘 : 仮称 "非特異性多発性小腸潰瘍症". 胃と腸 1968, 3 : 1539-1549
137) 崎村正弘 : "非特異性多発性小腸潰瘍症" の臨床的研究-限局性腸炎との異同を中心として-. 福岡医誌 1970, 61 : 318-340
138) 八尾恒良 : 非特異性小腸潰瘍. 臨床科学 1977, 13 : 789-797
139) 渡辺英伸 : 非特異性多発性小腸潰瘍症の病理組織学. 厚生省特定疾患消化吸収障害調査研究班昭和55年度業績集, 1980, 91-94
140) 岩下明徳, 黒岩重和, 山口幸二ほか : 小腸の潰瘍性病変の病理. 外科 1985, 47 : 1025-1033
141) 松井敏幸, 飯田三雄, 桑野恭行ほか : 非特異性多発性小腸潰瘍症の長期経過. 胃と腸 1989, 24 : 1157-1169
142) 松井敏幸, 八尾恒良, 青柳邦彦 : 非特異性多発性小腸潰瘍症. 胃と腸 1997, 32 : 459-468
143) Lindstrom CG : "Collagenous colitis" with watery diarrhoea- A new entity? Pathol Eur 1976, 11 : 87-89
148) 徳光陽一郎, 松浦隆志, 瀬尾充ほか : 移植片対宿主病 (graft-versus-host disease ; GVHD). 胃と腸 2003, 38 : 601-610
149) 長浜孝, 松井敏幸, 岩下明徳 : 里吉症候群. 胃と腸 2008, 44 : 713-718
151) 大泉弘子, 鈴木岳, 斎藤雅雄ほか : 大腸マラコプラキアの1例. 胃と腸 1998, 33 : 97-102
152) Ranchod M, Kahn LB : Malakoplakia of the gastrointestinal tract. Arch Pathol 1972, 94 : 90-97
155) 岩下明徳, 山田豊, 八尾建史ほか : 外科切除虫垂2,169例の臨床病理学的検索. 胃と腸 1990, 25 : 1185-1194
156) 吉良慎一郎, 加島健司, 駄阿 勉ほか : 虫垂脱落膜症の1例. 診断病理 2005, 22 : 166-168
158) Shperber J, Halevy A, Sayfan J et al : Congenital absence of the vermiform appendix. Isr J Med Sci 1983, 19 : 214-215
159) Collins DC : 71,000 human appendix specimens. A final report, summarizing forty years study. Am J Proctol 1963, 14 : 365-381
165) 宮地正彦, 蜂須賀喜多男, 山口晃弘ほか : 虫垂炎の臨床的検討. 日消外会誌 195, 18 : 952-960
166) Babekir ARE, Devi N : Analysis of the pathology of 405 appendices. East Afr Med J 1990, 67 : 599-602
167) Lindgren I, Aho AJ : Microangiographic investigations on acute appendicitis. Acta Chir Scand 1969, 135 : 77-82
168) Lau WY, Fan ST, Yiu TF et al : Acute appendicitis in the elderly. Surg Gynecol Obstet 1985, 161 : 157-160
170) Therkelsen F : On the histological diagnosis of appendicitis. Acta Chir Scand 1948, 94 (Suppl 108) : 1-48
171) Grossmann EB : Chronic appendicitis. Surg Gynecol Obstet 1978, 146 : 596-598
172) Al-Hilaly MA, Abu-Zidan FM, Zayed FF et al : Tuberculous appendicitis with perforation. Br J Clin Pract 1990, 44 : 632-633
176) Louw JH, Cywes S, Cremin BJ : Anorectal malformations. Classification and clinical features. S Afr J Surg 1971, 9 : 11-20
181) Goligher J : Anal fissure. in Surgery of the Anus, Rectum and Colon, 5th ed, Bailliere Tindall, 1984, 150-166
183) 佐藤太一, 山田一隆, 緒方俊二ほか : 痔瘻癌25例の臨床病理学的検討. 日消化器外会誌 2016, 49 : 579-587
184) 八尾隆史 : Crohn病の肛門病変の病理組織学的特徴. 胃と腸 2018, 53 : 975-978

13 腸管 - 腫瘍性疾患 -

P.604 掲載の参考文献
3) 宮木陽, 田中雄一, 小林芳生ほか : 直腸子宮内膜症より発生した類内膜腺癌の1例. 日消外会誌 2007, 40 : 1733-1738
4) 泉泰治, 松永浩明, 梶原正章ほか : 直腸, S字状結腸子宮内膜症の2例. 日消外会誌 1994, 27 : 932-936
6) 土屋智敬, 平松聖史, 尾辻英彦ほか : 直腸傍リンパ節に転移性病変を認めた直腸子宮内膜症の1例. 日消外会誌 2011, 72 : 418-422
9) 菅井有, 上杉憲幸, 杉本亮 : inflammatory myoglandular polyp と若年性ポリープの病理学的鑑別 inflammatory myoglandular polypの臨床病理学的特徴. 胃と腸 2013, 48 : 1161-1174
14) Klimstra DS, Nagtegaai ID, Rugge M et al : Tumours of small intestine. in WHO Classification of Tumours Editorial Board (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019, 112-134
21) 八尾隆史, 津山翔, 赤沢陽一ほか : 十二指腸腺腫と癌の病理組織学的診断基準. 胃と腸 2019, 54 : 1088-1094
27) 大腸癌研究会 (編) : 大腸癌取扱い規約, 第9版, 金原出版, 2018
28) Nagtegaai ID, Atends MJ, Odze RD et al : Tumors of the colon and rectum. in WHO Classification of Tumours Editorial Board (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019, 158-191
29) Yashiro M, Carethers JM, Laghi L et al : Genetic pathways in the evolution of morphologically distinct colorectal neoplasms. Cancer Res 2001, 61 : 2676-2683
30) 藤井隆広, 池松弘郎, 藤盛孝博 : 大腸villous tumorの定義と問題点-traditional serrated adenomaとの対比. Intetstine 2011, 15 : 507-515
31) 岩下明徳, 飯田光雄, 岩下俊光 : 大腸villous tumorの病理診断-生検診断, 癌化の問題を含む. 胃と腸 1986, 21 : 1303-1316
32) 工藤進英, 工藤由比, 笹島圭太ほか : LSTの定義. 早期大腸癌 2006, 10 : 377-382
33) 菅井有, 山野泰穂, 高木亮ほか : 大腸側方進展型腫瘍の臨床病理学的及び分子病理学的解析. 胃と腸 2010, 45 : 939-952
37) 菅井有, 中村眞一 : 大腸病変における免疫染色の有用性. 診断に役立つ免疫組織化学, 病理と臨床 2007, 25 (臨増) : 57-64
41) 菅井有, 山本英一郎, 木村友昭ほか : 大腸鋸歯状病変の臨床病理と分子異常. 日消誌 2015, 112 : 661-668
42) 菅井有, 山野泰穂, 木村友昭ほか : 大腸鋸歯状病変の臨床病理学的特徴と分子病理学的意義. 胃と腸 2011, 46 : 373-383
50) 八尾隆史, 菅井有, 岩下明徳ほか : 大腸SSA/Pの病理組織学的特徴と診断基準 大腸癌研究会プロジェクト研究から. 胃と腸 2011, 46 : 442-448
51) 菅井有, 山野泰穂, 木村友昭ほか : 消化管の病理 II-下部消化管-鋸歯状病変の病理診断および分子病理学的特徴. 病理と臨床 2011, 29 : 1065-1070
53) 菅井有, 永塚真, 田中義人 : 大腸鋸歯状病変の病理診断の課題と将来展望. 胃と腸 2019, 54 : 1491-1501
54) 菅井有, 永塚真, 田中義人 : 大腸粘膜内腫瘍における見方, 考え方, そのエビデンス. 病理と臨 2019, 37 : 748-756
57) 菅井有, 上杉憲幸, 幅野渉ほか : 遺伝性非ポリポージス大腸癌の臨床病理と分子異常-孤発性MSI陽性大腸癌との比較. 胃と腸 2010, 45 : 2065-2078
60) Pico MD, Castillejo A, Murcia O et al : Clinical and Pathological Characterization of Lynch-Like Syndrome. Clin Gastroenterol Hepatol 2019, pii : S1542-3565 (19) 30650-0
64) Briggs S, Tomlinson I : Germline and somatic polymerase ε and δ mutations define a new class of hypermutated colorectal and endometrial cancers. J Pathol 2013, 230 : 148-153
80) 菅井有, 上杉憲幸, 幅野渉ほか : 大腸低分化腺癌の腫瘍発生と分子異常. 胃と腸 2010, 45 : 1734-1748
83) Van Wyk HC, Foulis AK, Roxburgh CS et al : Comparison of Methods to Identify Lymphatic and Blood Vessel Invasion and their Prognostic Value in Patients with Primary Operable Colorectal Cancer. Anticancer Res 2015, 35 : 6457-6463
84) 松井敏幸, 津田純郎, 北原健二ほか : 早期大腸癌のX線診断. 1994, 32 : 77-85
88) 菅井有, 上杉憲幸, 遠藤昌樹ほか : そこが知りたい消化管病理深達度診断の標準化. 病理と臨床 2010, 28 : 635-641
94) Graham DM, Appelman HD : Crohn's-like lymphoid reaction and colorectal carcinoma : a potential histologic prognosticator. Mod Pathol 1990, 3 : 332-335
96) Biemer-Huttmann AE, Walsh MD, McGuckin MA et al : Mucin core protein expression in colorectal cancers with high levels of microsatellite instability indicates a novel pathway of morphogenesis. Clin Cancer Res 2000, 6 : 1909-1916
102) Boland CR, Thibodeau SN, Hamilton SR et al : A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition : development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 1998, 58 : 5248-5257
110) 岩渕三哉, 渡辺徹, 山貝悠ほか : 消化管内分泌細胞腫瘍の日本の分類と2010年WHO分類との対比. 胃と腸 2013, 48 : 941-955
111) 長村義之, 梶原博 : 神経内分泌腫瘍の病理診断-神経内分泌マーカーの発言と分子標的療法. 埼玉医大誌 2010, 37 : 84-85
113) 金子和弘, 冨田広, 牧野春彦ほか : 大腸転移をきたした乳腺浸潤性小葉癌の1例. 日臨外会誌 2006, 67 : 1237-1242
120) 中村昌太郎, 松本主之, 中村滋郎ほか : 腸管原発悪性リンパ腫の治療と予後. 胃と腸 2006, 41 : 323-337
122) 小篠洋之, 荒木靖三, 野明俊裕ほか : Colonic muco-submucosal elongated polypの1例. Gastroenterol Endosc 2011, 53 : 3776-3782
124) 赤松拓司, 山下幸孝, 松本久和ほか : S状結腸に発生したbenign fibroblastic polypの1例. Gastroenterol Endosc 2013, 55 : 3568-3572
131) 宇高徹総, 山本澄治, 中村哲也ほか : 原発性虫垂癌13例の臨床病理学的検討. 日外科系連会誌 2016, 41 : 738-742
133) Nagtegaai ID, Klimstra DS, Washington MK : Tumors of the appendix. in WHO Classification of Tumours Editorial Board (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019, 136-154
136) 菅井有, 上杉憲幸, 杉本亮ほか : 痔瘻癌の病理. 大腸癌Frontier 2013, 6 : 124-130
138) Goldblum JP, Kimstra DS, Lam AK : Tumors of the anal canal. in WHO Classification of Tumours Editorial Board (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019, 194-213
139) 高橋日出雄, 下田忠和, 石川栄世ほか : 痔瘻が関与した肛門部癌発生の病理学的検討. 大腸肛門誌 1982, 35 : 515-523
140) 隅越幸男, 岡田光生, 岩垂純一ほか : 痔瘻癌. 大腸肛門誌 1981, 4 : 467-472
141) 伊藤貴洋, 近藤昭信, 田中穣ほか : 粘膜内に限局した直腸肛門部悪性黒色腫の1例. 日消誌 2012, 109 : 435-441
143) 姚忠遠, 橋田裕穀, 貝原聡ほか : Paget現象との鑑別が困難であった肛門周囲Paget病の1例. 日臨外会誌 2013, 74 : 3430-3424

14 肝

P.675 掲載の参考文献
1) 大平弘正, 坂井田功 (編) : Hepatology Practice 4 難治性肝疾患の診療を極める-基本から最前線まで, 文光堂, 2014
2) 中沼安二 : 肝臓を診る医師のための肝臓病理テキスト, 南江堂, 2013
3) 中沼安二, 岡上武, 高瀬修二郎ほか : 肝小葉ゾーンからみた肝病態と臨床. 肝胆膵 2007, 55 : 149-162
4) 中沼安二, 坂元亨宇, 福嶋敬宜 (編) : キーワードとアルゴリズムでとらえる肝胆膵の実践病理診断, 文光堂, 2013
5) 原田憲一, 坂元亨宇 (編) : 肝臓 I : 肝病理診断のポイントびまん性肝疾患, 病理と臨床 2017, 35 : 206-266
6) 原田憲一, 坂元亨宇 (編) : 肝臓 II : 肝病理診断のポイント結節性肝病変, 病理と臨床 2017, 35 : 306-360
7) Burt A, Ferrell L, Hubscher S : MacSween's Pathology of the Liver, 7th ed, Elsevier, 2017
9) Lamps LW, Kakar S : Diagnostic Pathology : Hepatobiliary and Pancreas, 2nd ed, Elsevier, 2017
10) Lefkowitch JH : Scheuer's Liver Biopsy Interpretation, 9th ed, Elsevier, 2016
11) Saxena R : Practical Hepatic Pathology : A Diagnostic Approach 2nd Edition, Elsevier, 2017
12) WHO Classification of Tumours Editorial Board (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019
13) 恩地森一, 銭谷幹男, 山本和秀ほか : 自己免疫性肝炎の診断指針・治療指針 (2013年). 肝臓 2013, 54 : 723-725
14) 厚生労働省難治性疾患克服研究事業「難治性の肝・胆道疾患に関する調査研究」班 : 自己免疫性肝炎 (AIH) 診療ガイドライン (2016年), 2017
15) 原田憲一 : 急性肝炎期自己免疫性肝炎の病理. 肝臓 2018, 59 : 455-465
16) 藤澤知雄 : 小児の自己免疫性肝炎. Modern Physician 2017, 37 : 255-258
28) 岡上武, 西原利次, 小野正文ほか : 日本肝臓学会コンセンサス神戸 2009 NASHの診断と治療. 肝臓 2009, 50 : 741-747
29) 竹井謙之 (編) : Hepatology Practice 2 NASH・アルコール性肝障害の診療を極める-基本から最前線まで, 文光堂, 2013
30) 中野雅行 : 病理診断 : アルコール性肝障害肝組織所見と病型について. 竹井謙之竹, 持田智 (編) : NASH・アルコール性肝障害の診療を極める, 文光堂, 2013, 293-296
31) 日本肝臓学会 (編) : NAFLD の病理所見. NASH・NAFLDの診療ガイド 2015, 文光堂, 2015
39) Ludwig J, Viggiano TR, McGill DB et al : Nonalcoholic steatohepatitis : Mayo Clinic experience with a hitherto unnamed disease. Mayo Clin Proc 1980, 55 : 434-438
44) 中沼安二 : 胆道の病理-胆道と膵臓の潜在的可塑性から観察-. 胆道 2010, 24 : 73-81
60) 滝川一 : 薬物性肝障害の診断と治療 医学と医療の最前線. 日内会誌 2015, 104 : 991-997
61) 筒井朱美, 中沼安二, 佐藤保則 : 薬剤性コランギオパチー. 肝胆膵 2015, 71 : 861-868
68) 小林庸次, 奥山虎之 (編) : 先天性代謝異常. 病理と臨床 2004, 22 : 9-62
69) 藤澤知雄, 乾あやの, 河上牧夫 (編) : 小児臨床肝臓学-臨床と肝臓画像・病理-, 東京医学社, 2017
81) 中沼安二, 須藤嘉子 : 肝硬変 : progression, regression and remodeling-病因のいなくなった肝硬変の世界-. 肝胆膵 2016, 73 : 1056-1064
85) 日本移植学会, 日本病理学会 (編) : ヒト移植臓器拒絶反応の病理組織診断基準, 第2版, 金原出版, 2009
86) Demetris AJ, Bellamy C, Hubscher SG et al : 2016 Comprehensive Update of the Banff Working Group on Liver Allograft Pathology : Introduction of Antibody-Mediated Rejection. Am J Transplant 2016, 16 : 2816-2835
90) 中沼安二, 全陽, 湊宏 : 肝・胆道系感染症 : 感染症 病態と病理診断へのアプローチ, 病理と臨床 2003, 21 (臨増) : 307-323
91) 中沼安二, 橋本悦子, 松井修ほか : 肉芽腫性肝疾患の基礎と臨床. 肝胆膵 2008, 57 : 619-632
94) 坂元亨宇, 平岡伸介, 尾島英知 (編) : 癌診療指針のための病理診断プラクティス 肝・胆・膵腫瘍, 中山書店, 2014
95) 中沼安二, 坂元亨宇 (編) : 腫瘍病理鑑別診断アトラス 肝癌, 文光堂, 2010
96) 日本肝癌研究会 (編) : 臨床・病理 原発性肝癌取扱い規約, 第6版, 金原出版, 2015
97) 日本病理学会小児腫瘍組織分類委員会 (編) : 小児腫瘍組織分類図譜, 第4篇, 肝臓・胆嚢・脾臓腫瘍, 金原出版, 1998
132) 尾島英知 : 肝臓の胆管嚢胞腺癌・腺腫の病理学的特徴-膵臓の嚢胞腺癌・腺腫との比較を中心に-. 肝胆膵 2006, 52 : 205-211
133) 全陽, 中沼安二 : 胆道粘液産生性腫瘍の病理診断. 病理と臨床 2009, 27 : 546-553
134) 中沼安二 (編) : 胆道疾患を診る医師のための胆道病理テキスト, 南江堂, 2015
135) 日本肝胆膵外科学会 (編) : 胆道癌取扱い規約, 第6版, 金原出版, 2013
161) 近藤福雄, 副島友莉恵, 福里利夫 : 良性肝細胞性結節の病理診断 : 新WHO 分類をふまえて. 肝臓 2013, 54 : 807-818

15 胆嚢・胆管・十二指腸乳頭部

P.719 掲載の参考文献
1) 日本肝胆膵外科学会 (編) : 外科・病理 胆道癌取扱い規約, 第6版, 金原出版, 2013
3) WHO Classification of Tumours Editorial Boad (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019
4) 日本肝癌研究会 (編). 外科・病理 原発性肝癌取扱い規約, 第6版補訂版, 金原出版, 2019
5) 金子丑之助 : 日本人体解剖学, 第19版, 南山堂, 2000
6) Millis SE (ed) : Histology for Pathologists, 5th ed, Wolters Kluwer, 2020
7) 藤田尚男, 藤田恒夫 : 標準組織学-各論, 第4版, 医学書院, 2010
8) 吉澤忠司, 羽賀敏博, 鬼島 宏 : 胆嚢, 胆道. 病理診断に直結した組織学, 病理と臨床 2017, 35 (臨増) : 234-242
9) ムーア (原著) : 人体発生学, 原著第8版, 医歯薬出版, 2011
10) 中沼安二 (編著) : 胆道疾患を診る医師のための胆道病理テキスト, 南江堂, 2015
11) 葛西森夫, 沢口重徳, 秋山 洋ほか : 先天性胆道閉塞 (鎖) 症の新分類法試案. 日小外会誌 1976, 12 : 327-331
12) Alonso-Lej F, Rever WB Jr, Pessagno DJ : Congenital choledochal cyst, with a report of 2, and an analysis of 94 cases. Int Abst Surg 1959, 108 : 1-30
13) 戸谷拓二, 岡島邦雄, 田淵勝輔ほか. 先天性胆道拡張症その分類と手術方法および癌発生例について. 手術 1975, 29 : 875-880
14) 斎藤純夫, 古味信彦, 由良二郎ほか : 先天性胆道拡張症の新分類案. 日小児外会誌 1977, 13 : 817-819
15) 石橋広樹, 島田光生, 矢田圭吾 : 先天性胆道拡張症の診療ガイドライン (ダイジェスト版). 日消誌 2016, 113 : 2004-2015
16) 島田光生, 神澤輝実, 安藤久實ほか : 膵・胆管合流異常の診療ガイドライン. 胆道 2012, 26 : 678-690
17) 日本消化器病学会 (編) : 胆石症診療ガイドライン, 南江堂, 2009
18) 谷村弘, 内山和久 : 全国胆石症1996年度調査結果報告. 胆道 1997, 11 : 133-140
19) 田妻進, 菅野啓司, 窪田敬一ほか : 胆石症に関する2013年度全国調査結果報告. 胆道 2014, 28 : 612-617
20) 急性胆管炎・胆嚢炎診療ガイドライン改訂出版委員会 : 急性胆管炎・胆嚢炎診療ガイドライン 2018, 医歯薬出版, 2018
21) 鬼島宏, 渡辺英伸, 長村義之 : 胆道上皮の化生性変化と前癌病変. 病理と臨床 2003, 21 : 31-41
22) IgG4関連硬化性胆管炎臨床診断基準作成ワーキンググループ : IgG4関連硬化性胆管炎臨床診断基準 2012. 胆道 2012, 26 : 59-63
24) 羽賀敏博, 吉澤忠司, 鬼島宏 : 腫瘍様病変 (ポリープを含む) および腺筋腫症. 鬼島宏, 福嶋敬宜 (編) : 腫瘍病理鑑別診断アトラス 胆道癌・膵癌, 文光堂, 2015, 56-65
25) 守慶, 窪川芳広, 崔仁煥ほか : 胆嚢腺筋腫症に合併した胆嚢癌の臨床病理学的検討. 胆道 2010, 24 : 675-682
26) 日本肝胆膵外科学会, 胆道癌診療ガイドライン作成委員会 (編) : エビデンスに基づいた胆道癌診療ガイドライン, 第3版, 医学図書出版, 2019
27) 吉澤忠司, 鬼島宏 : 腺腫. 坂元亨宇, 平岡伸介, 尾島英知 (編) : 癌診療指針のための病理診断プラクティス 肝・胆・膵腫瘍, 中山書店, 2014
28) Albores-Saavedra J, Henson DE, Klimstra DS : Tumors of the Gallbladder, Extrahepatic Bile Ducts and Ampulla of Vater. Atlas of Tumor Pathology. 4th series, fascicle 23. Armed Forces Institute of Pathology (AFIP), 2015, 281-302, 323-374
30) 奈良井省吾, 大塚為和, 佐藤康行ほか : 総胆管壁に生じた断端神経腫の1例. 日臨外会誌 1985, 46 : 1137-1142
31) 福村由紀, 大池信之, 中沼安二ほか : 胆道癌の前癌病変 (IPNB, BilIN, ICPNを含む). 鬼島宏, 福嶋敬宜 (編) : 腫瘍病理鑑別診断アトラス 胆道癌・膵癌, 文光堂, 2015, 66-75
33) Albores-Saavedra J, Henson DE, Klimstra DS : Tumors of the Gallbladder, Extrahepatic Bile Ducts and Ampulla of Vater. Atlas of Tumor Pathology. 3rd series, fascicle 27. Armed Forces Institute of Pathology (AFIP), 1998
34) 日本胆道外科研究会 (編) : 外科・病理 胆道癌取扱い規約, 第5版, 金原出版, 2003
37) Yoshizawa T, Haga T, Goto S et al : Polypoid Neuroendocrine Tumor G1 of Gallbladder. Bio Med Res J 2020, 4 : 174-178
38) 吉澤忠司, 鬼島宏 : 神経内分泌腫瘍 (NET) および関連腫瘍 (パラガングリオーマを含む). 鬼島宏, 福嶋敬宜 (編) : 腫瘍病理鑑別診断アトラス 胆道癌・膵癌, 文光堂, 2015, 86-93
39) 平井秀明, 刀稱亀代志, 鬼島宏 : 術中迅速診断における鑑別, 判定, 報告 (細胞診の併用) 胆道. 鬼島宏, 福嶋敬宜 (編) : 腫瘍病理鑑別診断アトラス 胆道癌・膵癌, 文光堂, 2015, 245-250

16 膵

P.757 掲載の参考文献
1) Mills MD, Stacey E : Histology for Pathologists, 3rd ed, Lippincott Williams & Wilkins, 2006, 730-756
2) Hruban RH, Pitman MB, Klimstra DS : Tumors of the Pancreas, AFIP Atlas of Tumor Pathology, 4th Series, Fascicle 6, American Registry of Pathology, 2007, 1-22
3) 日本膵臓学会 (編) : 膵癌取扱い規約, 第7版, 金原出版, 2016, 59-63
6) Parsa I, Longnecker DS, Scarpelli DG et al : Ductal metaplasia of human exocrine pancreas and its association with carcinoma. Cancer Res 1985, 45 : 1285-1290
10) Hruban RH, Pitman MB, Klimstra DS : Tumors of the Pancreas, AFIP Atlas of Tumor Pathology, 4th Series, Fascicle 6, American Registry of Pathology, 2007, 367-369
13) 神澤輝実 : 膵先天性異常. 下瀬川徹 (編) : 新膵臓病学, 南江堂, 2017, 418-422
14) 西野隆義, 鬼澤俊輔, 濱野徹也ほか : 膵管癒合不全と輪状膵. 胆と膵 2015, 36 : 1213-1219
15) 栗原克己, 永井秀雄 : 副膵管・副乳頭の発生と解剖. 胆と膵 2015, 36 : 1205-1211
17) Hruban RH, Pitman MB, Klimstra DS : Tumors of the Pancreas, AFIP Atlas of Tumor Pathology, 4th Series, Fascicle 6, American Registry of Pathology, 2007, 349-351
18) 能登原憲司 : 膵病変の病理-炎症. 下瀬川徹 (編) : 新膵臓病学, 南江堂, 2017, 47-57
19) 正宗淳 : 慢性炎症-慢性膵炎. 下瀬川徹 (編) : 新膵臓病学, 南江堂, 2017, 331-332
21) 日本膵臓学会, 厚生労働科学研究費補助金 (難治性疾患等政策研究事業) 「IgG4関連疾患の診断基準並びに治療指針の確立を目指す研究」班 : 自己免疫性膵炎臨床診断基準 2018 (自己免疫性膵炎臨床診断基準 2011改訂版). 膵臓 2018, 33 : 902-913
22) 福嶋敬宜, 能登原憲司 : Lymphoplasmacytic sclerosing pancreatitis (LPSP) とidiopathic duct-centric chronic pancreatitis (IDCP) からみた自己免疫性膵炎. 肝胆膵 2008, 56 : 247-252
24) 岡崎和一 : 自己免疫性膵炎. 下瀬川徹 (編) : 新膵臓病学, 南江堂, 2017, 342-346
25) 三方林太郎, 石原武, 安井伸ほか : Groove pancreatitis. 胆と膵 2015, 36 : 1235-1240
30) Hruban RH, Pitman MB, Klimstra DS : Tumors of the Pancreas, AFIP Atlas of Tumor Pathology, 4th Series, Fascicle 6, American Registry of Pathology, 2007, 361-364
32) Hruban RH, Pitman MB, Klimstra DS : Tumors of the Pancreas, AFIP Atlas of Tumor Pathology, 4th Series, Fascicle 6, American Registry of Pathology, 2007, 360
37) Fukushima N, Hruban RH, Kato Y et al : Ductal adenocarcinoma variants and mixed neoplasms of the pancreas. in : Bosman FT, Carneiro F, Hruban RH et al (eds) : WHO Classification of Tumours of the Digestive System, 4th ed, IARC Press, 2010, 292-295
43) Adsay NV, Fukushima N, Furukawa T et al : Intraductal neoplasms of the pancreas. in Bosman FT, Carneiro F, Hruban RH et al (eds) : WHO Classification of Tumours of the Digestive System, 4th ed, IARC Press, 2010, 304-313
46) Basturk O, Esposit I, Fukushima N et al : pancreatic intraductal oncocytic papillary neoplasm. in WHO Classification of Tumours Editorial Board (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019, 315-316
47) Hruban RH, Boffetta P, Hiraoka N et al : Ductal adenocarcinoma of the pancreas. in Bosman FT, Carneiro F, Hruban RH et al (eds) : WHO Classification of Tumours of the Digestive System, 4th ed, IARC Press, 2010, 281-291
55) Singhi AD, Adsay NV, Hiraoka N et al : Serous neoplasms of the pancreas. in WHO Classification of Tumours Editorial Board (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019, 303-306
56) La Rosa S, Klimstra DS, Wood LD : Pancreatic acinar cell carcinoma. in WHO Classification of Tumours Editorial Board (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019, 333-336
58) Kloppel G, Adsay NV, Couvelard A : Pancreatic neuroendocrine neoplasms : introduction. in WHO Classification of Tumours Editorial Board (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019, 343-346
60) Hruban RH, Pitman MB, Klimstra DS : Tumors of the Pancreas, AFIP Atlas of Tumor Pathology, 4th Series, Fascicle 6, American Registry of Pathology, 2007, 251-304
65) Kloppel G, Basturk O, Klimstra DS et al : Solid pseudopapillary neoplasm of the pancreas. in WHO Classification of Tumours Editorial Board (ed) : WHO Classification of Tumours : Digestive System Tumours, 5th ed, IARC Press, 2019, 340-342

17 下垂体

P.780 掲載の参考文献
2) Stacey EM (ed) : Pituitary and sellar region. Histology for Pathologists, 3rd ed, Lippincott Williams and Wilkins. 2007, 321-344
11) Louis DN, Ohgaki H, Wiestler OD et al (eds) : WHO Classification of Tumours of the Central Nervous System, 4th ed, IARC Press, 2016, 324-328
12) Tihan T, Lopes MBS, Nishioka H et al : Craniopharyngioma. in : Lloyed RV, Osamura RY, Kloppel G et al (eds) : WHO Classification of Tumours of Endocrine Organs, 4th ed, IARC Press, 2017, 46-47
13) Sekine S, Shibata T, Kokubu A et al : Craniopharyngiomas of adamantinomatous type harbor β-catenin gene mutations. Am J Pathol 2002, 161 : 1997-2001
15) 日本脳神経外科学会, 日本病理学会 (編) : 脳腫瘍取扱い規約, 第4版, 金原出版, 2018, 148-153
17) Lloyd RV, Osamura RY, Kloppel G et al : WHO classification of tumours of the pituitary. in : Lloyd RV, Osamura RY, Kloppel G et al (eds) : WHO Classification of Tumours of Endocrine Organs, 4th ed, IARC Press, 2017, 12
21) DeLellis RA, Lloyed RV, Heitz PU et al : Pituitary tumours : Introduction. in : DeLellis RA, Lloyed RV, Heitz PU et al (eds) : WHO Classification of Tumours. Pathology and Genetics. Tumours of Endocrine Organs, 3rd ed, IARC Press, 2004, 10-39
24) Lloyed RV, Trouillas J, Kovacs K et al : Pituitary tumours : Introduction. in : DeLellis RA, Lloyed RV, Heitz PU et al (eds) : WHO Classification of Tumours. Pathology and Genetics. Tumours of Endocrine Organs, 3rd ed, IARC Press, 2004, 10-13
25) Osamura RY, Lopes MBS, Grossman A et al : Pituitary adenoma. in : Lloyd RV, Osamura RY, Kloppel G et al (eds) : WHO Classification of Tumours of Endocrine Organs, 4th ed, IARC Press, 2017, 14-18
27) Mete O, Korbonits M, Osamura RY et al : Somatotroph adenoma. in : Lloyd RV, Osamura RY, Kloppel G et al (eds) : WHO Classification of Tumours of Endocrine Organs, 4th ed, IARC Press 2017, 19-23
28) Kontogeorgos G, Kovacs K, Lloyd RV et al : Plurihormonal and double adenomas. in : Lloyd RV, Osamura RY, Kloppel G et al (eds) : WHO Classification of Tumours of Endocrine Organs, 4th ed, IARC Press, 2017, 39-40
33) George DH, Scheithauer BW, Kovacs K et al : Crooke's cell adenoma of the pituitary : an aggressive variant of corticotroph adenoma. Am J Surg Pthol 2003, 27 : 1330-1336
34) Hirohata T, Asano K, Ogawa Y et al : DNA mismatch repair protein (MSH6) correlated with the responses of atypical pituitary adenomas and pituitary carcinomas to temozolomide : the national cooperative study by the Japan Society for Hypothalamic and Pituitary Tumors. J Clin Endocrinol Metab 2013, 98 : 1130-1136
35) Lloyed RV, Osamura RY, Kloppel G et al : Tumours of the posterior pituitary, in : Lloyd RV, Osamura RY, Kloppel G et al (eds) : WHO Classification of Tumours of Endocrine Organs, 4th ed, IARC Press, 2017, 52-54
36) Mete O, Lopes MB, Asa SL : Spindle Cell Oncocytomas and Granular Cell Tumors of the Pituitary Are Variants of Pituicytoma. Am J Surg Pathol 2013, 37 : 1694-1699
37) Nagata Y, Inoshita N, Fukuhara N et al : Low-Grade Glioma of the Neurohypophysis : Clinical Characteristics and Surgical Outcomes. World Neurosurg 2018, 114 : e1225-e1231
38) Yoshimoto T, Takahashi-Fujigasaki J, Inoshita N et al : TTF-1-positive oncocytic sellar tumor with follicle formation/ependymal differentiation : non-adenomatous tumor capable of two different interpretations as a pituicytoma or a spindle cell oncocytoma. Brain Tumor Pathol 2015, 32 : 221-227

18 甲状腺

P.828 掲載の参考文献
1) Nikiforov YE, Biddinger PW, Thompson LD : Diagnostic Pathology and Molecular Genetics of the Thyroid : A Comprehensive Guide for Practicing Thyroid Pathology, 2nd ed. Wolters Kluwer Health, 2012
2) Lloyd RV, Douglas BD, Young WF : Atlas of Nontumor Pathology, Endocrine Diseases, AFIP, 2002
3) Rosai J, DeLellis RA, Carcangiu ML et al (eds) : AFIP Atlas of Tumor Pathology, Series 4, Tumors of the Thyroid and Parathyroid Glands, AFIP, 2014
4) 青笹克之, 長沼廣, 笹野公伸 (編) : 癌診療指針のための病理診断プラクティス, 内分泌腫瘍, 甲状腺, 副腎, 中山書店, 2018
5) 坂本穆彦, 廣川満良 (編) : 腫瘍病理鑑別診断アトラス 甲状腺癌, 文光堂, 2011
6) 宮章博, 宮内昭 : 甲状腺腫瘍の外科. 日内分泌・甲状腺外会誌 2012, 29 : 8-12
7) 甲状腺腫瘍診療ガイドライン作成委員会 (編) : 甲状腺腫瘍診療ガイドライン 2018. 日本内分泌・甲状腺外会誌 2018, 35 (Suppul 3) : 1-87
8) Haugen BR, Alexander EK, Bible KC et al : 2015 American Thyroid Association Management Guidelines for Adult Patients with Thyroid Nodules and Differentiated Thyroid Cancer : The American Thyroid Association Guidelines Task Force on Thyroid Nodules and Differentiated Thyroid Cancer. Thyroid 2016, 26 : 1-133
9) 日本乳腺甲状腺超音波医学会, 甲状腺用語診断基準委員会 (編) : 甲状腺超音波診断ガイドブック, 第3版, 南江堂, 2016
10) 日本内分泌外科学会/日本甲状腺病理学会 (編) : 甲状腺癌取扱い規約, 第8版, 金原出版, 2019
11) Ali SZ, Edmund S. Cibas ES : The Bethesda System for Reporting Thyroid Cytopathology : Definitions, Criteria, and Explanatory Notes, 2nd ed, Springer, 2018
12) Pueblitz S, Weinberg AG, Albores-Saavedra J : Thyroid C cells in the DiGeorge anomaly : a quantitative study. Pediatr Pathol 1993, 13 : 463-473
13) Miyauchi A, Matsuzuka F, Kuma K et al : Piriform sinus fistula and the ultimobranchial body. Histopathology 1992, 20 : 221-227
14) Suzuki A, Hirokawa M, Ito A et al : Derivation of thyroid lymphoepithelial cysts from follicular cells. Endocr J 2018, 65 : 579-586
15) Hirokawa M, Suzuki A, Miyauchi A : Comment on : Derivation of thyroid lymphoepithelial cysts from follicular cells. Endocr J 2018, 65 : 877-878
16) 日本甲状腺学会 (編) : 甲状腺専門医ガイドブック, 改訂第2版, 診断と治療社, 2018
17) 宮内昭 (監), 網野信行 (編) : 甲状腺・副甲状腺診療ゴールデンハンドブック, 南江堂, 2012
19) 志村浩己 : 日本における甲状腺腫瘍の頻度と経過-人間ドックからのデータ. 日甲状腺会誌 2010, 1 : 109-113
20) 武部晃司, 伊達学, 山本洋介ほか : 超音波検査を用いた甲状腺癌検診の実際とその問題点. Karkinos 1994, 7 : 309-317
21) Lloyd RV, Osamura RY, Kloppel G et al (eds) : WHO Classification of Tumours of Endocrine Organs, 4th ed, IARC Press, 2017
22) Volante M, Collini P, Nikiforov YE et al : Poorly differentiated thyroid carcinoma : the Turin proposal for the use of uniform diagnostic criteria and an algorithmic diagnostic approach. Am J Surg Pathol 2007, 31 : 1256-1264
23) Amin MB, Edge S, Greene F et al (eds) : AJCC Cancer Staging Manual, 8th ed, Springer, 2017
24) Mu N, Juhlin CC, Tani E et al : High Ki-67 index in fine needle aspiration cytology of follicular thyroid tumors is associated with increased risk of carcinoma. Endocrine 2018, 61 : 293-302
25) Williams ED : Two Proposals Regarding the Terminology of Thyroid Tumors. Int J Surg Pathol 2000, 8 : 181-183
26) Nikiforov YE, Seethala RR, Tallini G et al : Nomenclature Revision for Encapsulated Follicular Variant of Papillary Thyroid Carcinoma : A Paradigm Shift to Reduce Overtreatment of Indolent Tumors. JAMA Oncol 2016, 2 : 1023-1029
27) Carney JA, Ryan J, Goellner JR : Hyalinizing trabecular adenoma of the thyroid gland. Am J Surg Pathol 1987, 11 : 583-591
28) Hirokawa M, Carney JA : Cell membrane and cytoplasmic staining for MIB-1 in hyalinizing trabecular adenoma of the thyroid gland. Am J Surg Pathol. 2000, 24 : 575-578
29) Katoh R, Kakudo K, Kawaoi A : Accumulated basement membrane material in hyalinizing trabecular tumors of the thyroid. Mod Pathol. 1999, 12 : 1057-1061
30) Hirokawa M, Carney JA, Ohtsuki Y : Hyalinizing trabecular adenoma and papillary carcinoma of the thyroid gland express different cytokeratin patterns. Am J Surg Pathol 2000, 24 : 877-881
31) Pal T, Vogl FD, Chappuis PO et al : Increased risk for nonmedullary thyroid cancer in the first degree relatives of prevalent cases of nonmedullary thyroid cancer : a hospital-based study. J Clin Endocrinol Metab 2001, 86 : 5307-5312
32) Chang H, Kim SM, Chun KW et al : Clinicopathologic features of solid variant papillary thyroid cancer. ANZ J Surg 2014, 84 : 380-382
33) Enriquez ML, Baloch ZW, Montone KT et al : CDX2 expression in columnar cell variant of papillary thyroid carcinoma. Am J Clin Pathol 2012, 137 : 722-726
34) Hirokawa M, Kuma S, Miyauchi A et al : Morules in cribriform-morular variant of papillary thyroid carcinoma : Immunohistochemical characteristics and distinction from squamous metaplasia. APMIS 2004, 112 : 275-282
35) Akaishi J, Kondo T, Sugino K et al : Cribriform-Morular Variant of Papillary Thyroid Carcinoma : Clinical and Pathological Features of 30 Cases. World J Surg 2018, 42 : 3616-3623
36) Cameselle-Teijeiro JM, Peteiro-Gonzalez D, Caneiro-Gomez J et al : Cribriform-morular variant of thyroid carcinoma : a neoplasm with distinctive phenotype associated with the activation of the WNT/β-catenin pathway. Mod Pathol 2018, 31 : 1168-1179
37) Hirokawa M, Nishihara E, Takada N et al : Warthin-like papillary thyroid carcinoma with immunoglobulin G4-positive plasma cells possibly related to Hashimoto's thyroiditis. Endocr J 2018, 65 : 175-180
38) Takada N, Hirokawa M, Ito M et al : Papillary thyroid carcinoma with desmoid-type fibromatosis : A clinical, pathological, and immunohistochemical study of 14 cases. Endocr J 2017, 64 : 1017-1023
39) Miyauchi A, Ito Y : Conservative Surveillance Management of Low-Risk Papillary Thyroid Microcarcinoma. Endocrinol Metab Clin North Am 2019, 48 : 215-226
40) Sakamoto A, Kasai N, Sugano H : Poorly differentiated carcinoma of the thyroid. A clinicopathologic entity for a high-risk group of papillary and follicular carcinomas. Cancer 1983, 52 : 1849-1855
41) Sadow PM, Faquin WC : Poorly differentiated thyroid carcinoma : an incubating entity. Front Endocrinol (Lausanne) 2012, 3 : 77
42) Ito Y, Hirokawa M, Fukushima M et al : Prevalence and prognostic significance of poor differentiation and tall cell variant in papillary carcinoma in Japan. World J Surg 2008, 32 : 1535-1543
43) Ito Y, Miyauchi A, Hirokawa M et al : Prognostic value of the 8th tumor-node-metastasis classification for follicular carcinoma and poorly differentiated carcinoma of the thyroid in Japan. Endocr J 2018, 65 : 621-627
44) Suzuki A, Hirokawa M, Takada N et al : Diagnostic significance of PAX8 in thyroid squamous cell carcinoma. Endocr J 2015, 62 : 991-995
45) Kondo T, Ezzat S, Asa SL : Pathogenetic mechanisms in thyroid follicular-cell neoplasia. Nat Rev Cancer 2006, 6 : 292-306
46) Hirokawa M, Sugitani I, Kakudo K et al : Histopathological analysis of anaplastic thyroid carcinoma cases with long-term survival : A report from the Anaplastic Thyroid Carcinoma Research Consortium of Japan. Endocr J 2016, 63 : 441-447
47) Wells SA Jr, Asa SL, Dralle H et al : American Thyroid Association Guidelines Task Force on Medullary Thyroid Carcinoma. Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma. Thyroid 2015, 25 : 567-610
48) Verma A, Kane S, Vinarkar S et al : Small cell medullary thyroid carcinoma : A diagnostic dilemma. Indian J Pathol Microbiol 2017, 60 : 562-564
49) Hirokawa M, Kudo T, Ota H et al : Preoperative diagnostic algorithm of primary thyroid lymphoma using ultrasound, aspiration cytology, and flow cytometry. Endocr J 2017, 64 : 859-865
50) 廣川満良, 太田寿, 鈴木彩菜ほか : 甲状腺リンパ腫の診断. 内分泌糖尿代謝内科 2018, 47 : 93-97
51) Hirokawa M, Takada N, Abe H et al : Thyroid sclerosing mucoepidermoid carcinoma with eosinophilia distinct from the salivary type. Endocr J 2018, 65 : 427-436
52) Dorfman DM, Shahsafaei A, Miyauchi A : Intrathyroidal epithelial thymoma (ITET) /carcinoma showing thymus-like differentiation (CASTLE) exhibits CD5 immunoreactivity : new evidence for thymic differentiation. Histopathology 1998, 32 : 104-109
53) Miyauchi A, Kuma K, Matsuzuka F et al : Intrathyroidal epithelial thymoma : an entity distinct from squamous cell carcinoma of the thyroid. World J Surg 1985, 9 : 128-135
54) Hirokawa M, Miyauchi A, Minato H et al : Intrathyroidal epithelial thymoma/carcinoma showing thymus-like differentiation, comparison with thymic lymphoepithelioma-like carcinoma and a possibility of development from a multipotential stem cell. APMIS 2013, 121 : 523-530
55) Kobayashi K, Hirokawa M, Yabuta T et al : Metastatic carcinoma to the thyroid gland from renal cell carcinoma : role of ultrasonography in preoperative diagnosis. Thyroid Res 2015, 8 : 4
56) Suzuki A, Hirokawa M, Takada N et al : Fine-needle aspiration cytology for medullary thyroid carcinoma : a single institutional experience in Japan. Endocr J 2017, 64 : 1099-1104
57) Takada N, Hirokawa M, Ito A et al : Cytoplasmic Lipid Accumulation Characteristic of the Cribriform Variant of Papillary Thyroid Carcinoma. Pathobiology 2017, 84 : 251-257
58) Pyo JS, Kim DH, Yang J : Diagnostic value of CD56 immunohistochemistry in thyroid lesions. Int J Biol Markers 2018, 33 : 161-167
59) Takada N, Hirokawa M, Ohbayashi C et al : Re-evaluation of MIB-1 immunostaining for diagnosing hyalinizing trabecular tumour of the thyroid : semi-automated techniques with manual antigen retrieval are more accurate than fully automated techniques. Endocr J 2018, 65 : 239-244
60) Suzuki A, Hirokawa M, Takada N et al : Utility of monoclonal PAX8 antibody for distinguishing intrathyroid thymic carcinoma from follicular cell-derived thyroid carcinoma. Endocr J 2018, 65 : 1171-1175
61) Takada N, Hirokawa M, Suzuki A et al : Diagnostic value of GATA-3 in cytological identification of parathyroid tissues. Endocr J 2016, 63 : 621-626
62) Ito Y, Miyauchi A, Kakudo K, Hirokawa M et al : Prognostic significance of Ki-67 labeling index in papillary thyroid carcinoma. World J Surg 2010, 34 : 3015-3021
63) 加藤良平 : 甲状腺癌の遺伝子診断は有用か? 日内分泌・甲状腺外会誌 2017, 34 : 88-92
64) 菅間博, 住石歩, 千葉知宏ほか : 甲状腺腫瘍の遺伝子診断と細胞診. 日内分泌・甲状腺外会誌 2014, 31 : 125-129
65) 光武範吏 : 甲状腺未分化癌の網羅的遺伝子解析 : 最新の研究成果のレビュー. 日内分泌・甲状腺外会誌 2016, 33 : 161-165

19 副甲状腺

P.845 掲載の参考文献
1) Sasano H, Geelhoed GW, Silverberg SG : Intraoperative cytologic evaluation of lipid in the diagnosis of parathyroid adenoma. Am J Surg Pathol 1988, 12 : 282-286
2) Lieberman A, DeLellis RA : Intrafollicular amyloid in normal parathyroid gland. Arch Pathol 1973, 95 : 422-423
3) Katoh R, Kawaoi A, Muramatsu A et al : Birefringent (calcium oxalate) crystals in thyroid diseases. A clinicopathological study with possible implications for different diagnosis. Am J Surg Pathol 1993, 17 : 698-705
4) Glimerius L, Akerstrom G, Johansson H et al : The parathyroid glands. in : Kovacs K, Asa S (eds) : Functional Endocrine Pathology, Vol.1, Blackwell Scientific, 1991, 375-395
5) Ozcan A, Shen SS, Hamilton C et al : PAX-8 expression in non-neoplastic tissue, primary tumors and metastatic tumors : a comprehensive immunohistochemical study. Mod Pathol 2011, 24 : 751-764
6) Veras E, Sturgis EM, Luna MA : Heterotopic parathyroid inclusion in a cervical lymph node. Head Neck 2007, 29 : 1160-1163
7) Yousef GM, Denic N, Wadhwa J et al : Intravagal ectopic parathyroid presenting as vocal cord paralysis : case report and review of the literature. J Otolaryngol 2007, 36 : E93-E95
8) Papavramidis TS, Chorti A, Pliakos I et al : Parathyroid cysts : A review of 359 patients reported in the international literature. Medicine 2018, 97 : 28
9) Baloch ZW, LiVolsi VA : Pathology of the parathyroid glands in hyperparathyroidism, Sem Diagn Pathol 2013, 30 : 165-177
10) Reddick RL, Costa JC, Marx SJ : Parathyroid hyperplasia and parathyromatosis. Lancet 1977, 1 : 549
11) Shen WT : Parathyromatosis and parathyroid cancer. Cancer Treat Res 2010, 153 : 105-116
12) Fernandez-Ranvier GG, Khanafsha E, Jensen K et al : Parathyroid carcinoma, atypical parathyroid adenoma, or parathyromatosis? Cancer 2007, 110 : 255-264
13) Baloch ZW, Fraker D, LiVolsi VA : Parathyromatosis as cause of recurrent secondary hyperparathyroidism : A cytologic diagnosis. Diagn Cytopathol 2001, 25 : 403-405
14) Kendrick ML, Charboneau JW, Curlee KJ et al : Risk of parathyromatosis after fine-needle aspiration. Am Surg 2001, 67 : 290-294
15) Snover DC, Foucar K : Mitotic activity in benign parathyroid disease. Am J Clin Pathol 1981, 75 : 345-347
16) Howson P, Kruijff S, Aniss A et al : Oxyphil cell parathyroid adenomas causing primary hyperparathyroidism : a clinicopathological correlation. Endocr Pathol 2015, 26 : 250-254
17) Guiter GE, DeLellis RA : Risk of recurrence or metastasis in atypical parathyroid adenomas. Mod Pathol 2002, 15 : 115A
18) Kruijff S, Sidhy SB, Sywak MS et al : Negative parafibromin staining predicts malignant behavior in atypical parathyroid adenomas. Ann Surg Oncol 2014, 21 : 426-433
19) Shantz A, Castleman B : Parathyroid carcinoma. A study of 70 cases. Cancer 1973, 31 : 600-605
20) Kameyama K, DeLellis RA, Lloyd RV et al : Parathyroid carcinomas : can clinical outcomes for parathyroid carcinomas be determined by histologic evaluation alone? Endocr Pathol 2001, 13 : 135-139
21) Kameyama K, Takami H, Sanders D et al : Surgical pathology of hyperparathyroidism. Biomed Pharmacother 2000, 54 (Suppl 1) : 42s-45s
22) Sandelin K, Tullgreen O, Farnebo LO : Clinical course of metastatic parathyroid carcinoma. World J Surg 1994, 18 : 594-598
23) Ippolito G, Palazzo FF, Sebag F et al : Intraoperative diagnosis and treatment of parathyroid cancer and atypical parathyroid adenoma. Br J Surg 2007, 94 : 566-570
24) Bondeson L, Grimelius L, DeLellis RA et al : Parathyroid carcinoma. in : DeLellis RA, Lloid RV, Heitz PU et al (eds) : WHO Classification of Tumours. Pathology and Genetics. Tumours of Endocrine Organs. IARC Press, 2004, 124
25) Talat N, Schulte K : Clinical presentation, staging and long-term evolution of parathyroid cancer. Ann Surg Oncol 2010, 17 : 2156-2174
26) Schulte K, Talat N : Diagnosis and management of parathyroid cancer. Nat Rev Endocrinol 2012, 8 : 612-622
27) Kameyama K, Takami H : Proposal for the histological classification of parathyroid carcinoma. Endocr Pathol 2005, 16 : 49-52
28) Kameyama K, Takami H, Umemura S et al : PCNA and Ki-67 as prognostic markers in human parathyroid carcinomas. Ann Surg Oncol 2000, 7 : 301-304
29) Obara T, Fujimoto Y, Yamaguchi K et al : Parathyroid carcinoma of the oxyphil type : a report of two cases, light and electron microscopic study. Cancer 1985, 55 : 1482-1489
30) Erickson LA, Jin L, Papotti M et al : Oxyphil parathyroid carcinomas : a clinicopathologic and immunohistochemical study of 10 cases. Am J Surg Pathol 2001, 26 : 344-349
31) Capten JD, Robbins CM, Villablanca A et al : HRPT2 encoding parafibromin is mutated in hyperparathyroidism-jaw tumor syndrome. Nat Genet 2002, 32 : 676-680
32) Howell VM, Haven CJ, Kahnoski K et al : HRPT2 mutations are associated with malignancy in sporadic parathyroid tumors. J Med Genet 2003, 40 : 657-663
33) Shattuck TM, Valimaki S, Obara T et al : Somatic and germline mutation of the HRPT2 gene in sporadic parathyroid carcinoma. N Engl J Med 2003, 349 : 1722-1729
34) Tan MH, Morisson C, Wang P et al : Loss of parafibromin immunoreactivity is a distinguishing feature of parathyroid carcinoma. Clin Cancer Res 2004, 10 : 6629-6637
35) Kumari N, Chaudhary N, Pradhan R et al : Role of histological criteria and immunohistochemical markers in predicting risk of malignancy in parathyroid neoplasms. Endocr Pathol 2016, 27 : 87-96
36) DeLellis RA, Mazzaglia P, Mangray S : Primary hyperparathyroidism. A current perspective. Arch Pathol Lab Med 2008, 132 : 1251-1262
37) Christmas TJ, Chapple CR, Noble JG et al : Hyperparathyroidism after neck irradiation. Br J Surg 1988, 75 : 873-874
38) Awad SS, Miskulin J, Thompson N : Parathyroid adenomas versus four-gland hyperplasia as the cause of primary hyperparathyroidism in patients with prolonged lithium therapy. World J Surg 2003, 27 : 486-488
39) Clark OH, Okerlund MD, Cavalieri RR et al : Diagnosis and treatment of thyroid, parathyroid, and thyroglossal duct cysts. J Clin Endocloinol Metab 2007, 48 : 983-988
40) De Gregorio L, Lubitz CC, Hodin RA et al : The truth about double adenomas : incidence, localization, and intraoperative parathyroid hormone. J Am Coll Surg 2016, 222 : 1044-1052
41) Harach HR, Jasani B : Parathyroid hyperplasia in tertiary hyperparathyroidism : a pathological and immunohistochemical reappraisal. Histopathology 1992, 21 : 513-520
42) Kabebew E, Duh QY, Clark OH : Tertiary hyperparathyroidism. Histologic patterns of disease and results of parathyroidectomy. Arch Surg 2004, 139 : 974-977
43) Takami H, Shirahama S, Ikeda Y et al : Familial hyperparathyroidism. Biomed Pharmacother 2000, 54 (Suppl 1) : 21s-24s
44) Kameyama K, Takami H : Medullary thyroid carcinoma : nationwide Japanese survey of 634 cases in 1996 and 271 cases in 2002. Endocr J 2004, 51 : 453-456

20 副腎・傍神経節

P.873 掲載の参考文献
1) Sasano H : New approaches in human adrenocortical pathology : Assessment of adrenocortical function in surgical specimen of human adrenal glands. Endocr Pathol 1992, 3 : 4-13
2) Sasano H : Localization of steroidogenic enzymes in adrenal cortex and its disorders. Endocr J 1994, 41 : 471-482
3) Narasaka T, Suzuki T, Moriya T et al : Temporal and spatial distribution of corticosteroidogenic enzymes immunoreactivity in developing human adrenal. Mol Cell Endocrinol 2001, 174 : 111-120
4) Gell JS, Carr BR, Sasano H et al : Adrenarche results from development of a 3beta-hydroxysteroid dehydrogenase-deficient adrenal reticularis. J Clin Endocrinol Metab 1998, 83 : 3695-3701
5) Suzuki T, Sasano H, Takeyama J et al : Developmental changes in steroidogenic enzymes in human postnatal adrenal cortex : Immunohistochemical studies. Clin Endocrinol (Oxf) 2000, 53 : 739-747
6) Sasano H, Mason JI, Sasano N : Immunohistochemical study of cytochrome P-450 17 alpha in human adrenocortical disorders. Hum Pathol 1989, 20 : 113-117
7) Gomez-Sanchez CE, Qi X, Velarde-Miranda C et al : Development of monoclonal antibodies against human CYP11B1 and CYP11B2. Mol Cell Endocrinol 2013, 383 : 111-117
8) Nakamura Y, Kitada M, Satoh F et al : Intratumoral heterogeneity of steroidogenesis in aldosterone-producing adenoma revealed by intensive double- and triple-immunostaining for CYP11B2/B1 and CYP17. Mol Cell Endocrinol 2016, 422 : 57-63
9) Sasano H, Mason JI, Sasano N et al : Immunolocalization of 3beta-hydroxylase dehydrogenase (3beta-HSD) in human adrenal cortex and its disorders. Endocr Pathol 1990, 1 : 94-101
10) Sasano H, Sato F, Shizawa S et al : Immunolocalization of dehydroepiandrosterone sulfotransferase in normal and pathologic human adrenal gland. Mod Pathol 1995, 8 : 891-896
11) Omata K, Anand SK, Hovelson DH et al : Aldosterone-Producing Cell Clusters Frequently Harbor Somatic Mutations and Accumulate With Age in Normal Adrenals. J Endocr Soc 2017, 1 : 787-799
12) Suzuki T, Takahashi K, Darnel AD et al : Chicken ovalbumin upstream promoter transcription factor II in the human adrenal cortex and its disorders. J Clin Endocrinol Metab 2000, 85 : 2752-2757
13) Sasano H, Shizawa S, Suzuki T et al : Ad4BP in the human adrenal cortex and its disorders. J Clin Endocrinol Metab 1995, 80 : 2378-2380
14) Hasegawa T, Zhao L, Caron KM et al : Developmental roles of the steroidogenic acute regulatory protein (StAR) as revealed by StAR knockout mice. Mol Endocrinol 2000, 14 : 1462-1471
15) Sasano H, Imatani A, Shizawa S et al : Cell proliferation and apoptosis in normal and pathologic human adrenal. Mod Pathol 1995, 8 : 11-17
16) Sasano H, Ohashi Y, Suzuki T et al : Vascularity in human adrenal cortex. Mod Pathol 1998, 11 : 329-333
17) Yaguchi H, Tsutsumi K, Shimono K et al : Involvement of high density lipoprotein as substrate cholesterol for steroidogenesis by bovine adrenal fasciculo-reticularis cells. Life Sci 1998, 62 : 1387-1395
18) Beckwith JP : Macroglossia, omphalocele, adrenal cytomegaly, gigantism and hyperplastic visceromegaly. Birth Defects Orig Art Ser 1969, 5 : 188-196
19) Candida Barisson Villares Fragoso M, Pontes Cavalcante I, Meneses Ferreira A et al : Genetics of primary macronodular adrenal hyperplasia. Presse Med 2018, 47 (7-8 Pt 2) : e139-e149
20) Velayoudom-Cephise FL, Haissaguerre M, Tabarin A : Etiopathogeny of Primary Adrenal Hypercortisolism. Front Horm Res 2016, 46 : 39-53
21) Sasano H, Suzuki T, Nagura H : ACTH-independent macronodular adrenocortical hyperplasia : Immunohistochemical and in situ hybridization studies of steroidogenic enzymes. Mod Pathol 1994, 7 : 215-219
22) Sasano H, Miyazaki S, Sawai T et al : Primary pigmented nodular adrenocortical disease (PPNAD) : Immunohistochemical and in situ hybridization analysis of steroidogenic enzymes in eight cases. Mod Pathol 1992, 5 : 23-29
23) Chute AL, Robinson GC, Donohue WL : Cushing's syndrome in children. J Pediatr 1949, 34 : 20-28
24) Carney JA, Gordon H, Carpenter PC et al : The complex of myxomas, spotty pigmentation and endocrine overactivity. Medicine (Baltimore) 1985, 64 : 270-283
25) Carney JA, Hruska LS, Beauchamp GD et al : Dominant inheritance of myxomas, spotty pigmentation and endocrine overactivity. Mayo Clin Proc 1986, 61 : 165-172
26) Kirschner LS, Carney JA, Pack SD et al : Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex. Nat Genet 2000, 26 : 89-92
27) Horvath A, Boikos S, Giatzakis C et al : A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia. Nat Genet 2006, 38 : 794-800
28) Sasano H : Adrenocortical oncocytoma. A true nonfunctioning adrenocortical tumor. Am J Surg Pathol 1991, 15 : 949-956
29) Bisceglia M, Ludovico O, Di Mattia A et al Adrenocortical oncocytic tumors : report of 10 cases and review of the literature. Int J Surg Pathol 2004, 12 : 231-243
30) Wong DD, Spagnolom DV, Biscegliam M et al : Oncocytic adrenocortical neoplasms - a clinicopathologic study of 13 new cases emphasizing the importance of their recognition. Hum Pathol 2011, 42 : 489-499
31) Cohn K, Gottesman L, Brennan MF : Adrenocortical carcinoma. Surgery 1986, 100 : 1170-1177
32) Sasano H, Suzuki T, Nagura H et al : Steroidogenesis in human adrenocortical carcinoma : Biochemical activities, immunohistochemistry, and in situ hybridization of steroidogenic enzymes and histopathologic study in nine cases. Hum Pathol 1993, 24 : 397-404
33) Sasano H : Adrenal cortex. in : Sasano H, Stefaneanu L, Kovacs K (eds) : Molecular and Cellular Endocrine Pathology, Chapman and Hall Publishing Company, 1999, 221-252
34) Tang CK, Gray GF : Adrenocortical neoplasms. Prognosis and morphology. Urology 1975, 5 : 691-695
35) Gandour MJ, Grizzle WE : A small adrenocortical carcinoma with aggressive behavior. An evaluation of criteria for malignancy. Arch Pathol Lab Med 1986, 110 : 1076-1079
36) Hough AJ, Hollifield JW, Page DL et al : Prognostic factors in adrenal cortex tumors : A mathematical analysis of clinical and morphological data. Am J Clin Pathol 1979, 72 : 390-399
37) Weiss LM : Comparable histologic study of 43metastasizing and nonmetastasizing adrenocortical tumors. Am J Surg Pathol 1984, 8 : 163-169
38) Weiss LM, Medeiros LJ, Vickery AL : Pathologic features of prognostic significance in adrenocortical carcinoma. Am J Surg Pathol 1989, 13 : 202-206
39) Slooten HV, Schaberg A, Smeenk D et al : Morphologic characteristics of benign and malignant adrenocortical tumors. Cancer 1985, 55 : 766-773
40) Wieneke JA, Thompson LD, Heffess CS : Adrenal cortical neoplasms in the pediatric population : a clinicopathologic and immunophenotypic analysis of 83 patients. Am J Surg Pathol 2003, 27 : 867-881
41) Papotti M, Volante M, Duregon E et al, Adrenocortical tumors with myxoid features : a distinct morphologic and phenotypical variant exhibiting malignant behavior. Am J Surg Pathol 2010, 34 : 973-983
42) Suzuki T, Sasano H, Nishikawa T et al : Discerning malignancy in human adrenocortical neoplasms : Utility of DNA flow cytometry and immunohistochemistry. Mod Pathol 1992, 5 : 224-231
43) Zhao J, Speel EJ, Muletta-Feurer S et al : Analysis of genomic alterations in sporadic adrenocortical lesions. Gain of chromosome 17 is an early event in adrenocortical tumorigenesis. Am J Pathol 1999, 155 : 1039-1045
44) Russell AJ, Sibbald J, Haak H et al : Increasing genome instability in adrenocortical carcinoma progression with involvement of chromosomes 3, 9 and X at the adenoma stage. Br J Cancer 1999, 81 : 684-689
45) Lloyd R, Osamura RY, Kloppel G et al (eds) : WHO Classification of Tumours of Endocrine Organs, 4th ed, IARC Press, 2017
46) Iino K, Sasano H, Yabuki N et al : DNA topoisomerase IIa and Ki-67 in human adrenocortical neoplasms : A possible marker of differentiation between adenomas and carcinomas. Mod Pathol 1997, 10 : 901-907
47) Yamazaki Y, Nakamura Y, Shibahara Y et al, Comparison of the methods for measuring the Ki-67 labeling index in adrenocortical carcinoma : manual versus digital image analysis. Hum Pathol 2016, 53 : 41-50
48) McNicol A : Adrenal medullar and paraganglia. in : Llyod RV (ed) : Endocrine Pathology, Humana Press, 2004, 227-243
49) Kimura N : The adrenal medulla and extra-adrenal paraganglis. in : Sasano H, Stefaneanu L, Kovacs K (eds) : Molecular and Cellular Endocrine Pathology, Arnold, 2000, 253-264
50) Thompson LD : Pheochromocytoma of the adrenal gland scaled score (PASS) to separate benign from malignant neoplasms ; A clinicopathologic and immunophenotypic study of100cases. Am J Surg Pathol 2002, 26 : 551-566
51) Grouzmann E, Gicquel G, Plouin PF et al : Neuropeptide Y and neuron specific enolase levels in benign and malignant pheochromocytomas. Cancer 1990, 66 : 1833-1835
52) van der Harst E, Bruining HA, Jaap Bonjer H : Proliferative index in pheochromocytoma : Does it predict the occurrence of metastasis? J Pathol 2000, 191 : 175-180
53) Clarke MR, Weyant RJ, Watson CG et al : Prognostic markers in pheochromocytoma. Hum Pathol 1998, 29 : 522-526
54) Sastry P, Tocock A, Coonar AS et al : Adrenalectomy for isolated metastasis from operable non-small-cell lung cancer. Interact Cardiovasc Thorac Surg 2014, 18 : 495-497
55) Stone WZ, Wymer DC, Canales BK : Fluorodeoxyglucose-positron-emission tomography/computed tomography imaging for adrenal masses in patients with lung cancer : review and diagnostic algorithm. J Endourol 2014, 28 : 104-111
56) Pfister C : Adrenal biopsy is recommended to differentiate benign versus malignant metastasis of primary adrenal lesions. AJR Am Roentgenol 2014, 203 : 340-351
57) Mondal SK, Dasgupta S, Mandal PK et al : Cytodiagnosis of myxoid adrenocortical carcinoma and role of immunocytochemistry to differentiate it from renal cell carcinoma. J Cytol 2014, 31 : 111-113
58) Kitawaki Y, Nakamura Y, Kubota-Nakayama F et al : Tumor Microenvironment in Functional Adrenocortical Adenomas : Immune Cell Infiltration in Cortisol-producing Adrenocortical Adenoma. Hum Pathol 2018, 77 : 88-97
P.918 掲載の参考文献
1) 坂井建雄, 河原克雅 : 腎・泌尿器. カラー図解人体の正常構造と機能, 日本医事新報社, 1999, 6-35
2) 坂井建雄 : 初心者のための腎臓の構造. 日腎誌 2001, 43 : 572-579
3) Zhou XJ, Laszik ZG, Nadasdy T et al (eds) : Silva's Diagnostic Renal Pathology, 2nd ed, Cambridge Medicine, 2017, 57-91
4) 長田道夫, 門川俊明 : なぜパターン認識だけでは腎病理は読めないのか? 医学書院, 2017
5) 山中宣昭 : 腎生検に必要な各種染色法. 腎生検病理アトラス, 改訂版, 東京医学社, 2017, 32-43
6) Haas M : A reevaluation of routine electron microscopy in the examination of native renal biopsies. J Am Soc Nephrol 1977, 8 : 70-76
7) Weening JJ, D'Agati VD, Schwartz MM et al : The classification of glomerulonephritis in systemic lupus erythematosus revisited. J Am Soc Nephrol 2004, 15 : 241-250
8) 長田道夫, 益澤尚子, 本田一穂ほか : 腎生検病理診断取扱い規約, 金原出版, 2019, 9-19
9) Sethi S, Haas M, Markowitz G et al : Mayo Clinic/renal pathology society consensus report on pathologic classification, diagnosis, and reporting of GN. J Am Soc Nephrol 2016, 27 : 1278-1287
10) Rosenberg AZ, Kopp JB : Focal Segmental Glomerulosclerosis. Clin J Am Soc Nephrol 2017, 12 : 502-517
11) Sadowski CE, Lovric S, Ashraf S et al : A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome. J Am Soc Nephrol 2015, 26 : 1279-1289
12) Lovric S, Ashraf S, Tan W et al : Genetic testing in steroid-resistant nephrotic syndrome : when and how? Nephrol Dial Transplant 2016, 31 : 1802-1813
13) D'Agati VD, Fogo A, Bruijn JA et al : Pathologic classification of focal segmental glomerulosclerosis : a working proposal. Am J Kidney Dis 2004, 43 : 368-382
14) Berger J, Hinglais N : Les depots intercapillaires d'IgA-IgG. J Urol Nephrol 1968, 74 : 694-695
15) Katafuchi R, Ninomiya T, Nagata M et al : Validation study of oxford classification of IgA nephropathy : the significance of extracapillary proliferation. Clin J Am Soc Nephrol 2011, 6 : 2806-2813
16) Saha MK, Julian BA, Novak J et al : Secondary IgA nephropathy. Kidney Int 2018, 94 : 674-681
17) Roberts IS, Cook HT, Troyanov S et al : The Oxford classification of IgA nephropathy : pathology definitions, correlations, and reproducibility. Kidney Int 2009, 76 : 546-556
18) 松尾清一 (監), 厚生労働省難治性疾患克服研究事業進行性腎障害に関する調査研究班 (編) : エビデンスに基づくIgA腎症診療ガイドライン 2014, 東京医学社, 2015, 40-54
19) Beck LH Jr : PLA2R and THSD7A : Disparate Paths to the Same Disease? J Am Soc Nephrol 2017, 28 : 2579-2589
20) Zhou XJ, Silva F : Membranoproliferative glomerulonephritis. in : Jennette JC, Olson JL, Silva FG et al (eds) ; Heptinstall's Pathology of the Kidney, 7th ed, Wolters Kluwer, 2015, 301-340
21) Pickering MC, D'Agati VD, Nester CM et al : C3 glomerulopathy : consensus report. Kidney Int 2013, 84 : 1079-1089
22) Kawamura T, Usui J, Kaseda K et al : Primary membranoproliferative glomerulonephritis on the decline : decreased rate from the 1970s to the 2000s in Japan. Clin Exp Nephrol 2013, 17 : 248-254
23) Ito N, Ohashi R, Nagata M : C3 glomerulopathy and current dilemmas. Clin Exp Nephrol. 2017, 21 : 541-551
24) Song D, Wu LH, Wang FM et al : The spectrum of renal thrombotic microangiopathy in lupus nephritis. Arthritis Res Ther 2013, 15 : R12
25) Furuichi K, Yuzawa Y, Shimizu M et al : Nationwide multicentre kidney biopsy study of Japanese patients with type 2 diabetes. Nephrol Dial Transplant 2018, 33 : 138-148
26) Alicic RZ, Rooney MT, Tuttle KR : Diabetic kidney disease : Challenges, Progress, and Possibilities. Clin J Am Soc Nephrol 2017, 12 : 2032-2045
27) 日本腎臓学会 (編) : エビデンスに基づくCKD診療ガイドライン, 東京医学社, 2018, 104-110
28) Mise K, Yamaguchi Y, Hoshino J et al : Paratubular basement membrane insudative lesions predict renal prognosis in patients with type 2 diabetes and biopsy-proven diabetic nephropathy. PLoS One 2017, 12 : e0183190
29) Glassock RJ, Alvarado A, Prosek J et al : Staphylococcus related glomerulonephritis and poststreptococcal glomerulonephritis : why defining "post" is important in understanding and treating infection-related glomerulonephritis. Am J Kidney Dis 2015, 65 : 826-832
30) Oda T, Yoshizawa N, Yamanaka K et al : The role of nephritis-associate plasmin receptor (NAPLr) in glomerulonephritis associated with streptococcal infection. J Biomed Biotech 2012, 2012 : 417675
31) Koyama A, Sharmin S, Sakurai H et al : Staphylococcus aureus cell envelope antigen is a new candidate for the induction of IgA nephropathy. Kidney Int 2004, 66 : 121-132
32) Ozkok A, Yildiz A : Hepatitis C virus associated glomerulopathies. World J Gastroenterol 2014, 20 : 7544-7554
33) Swanepoel CR, Atta MG, D'Agati VD, et al : Kidney disease in the setting of HIV infection : conclusions from a Kidney Disease : Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int 2018, 93 : 545-559
34) Moal V, Zandotti C, Colson P et al : Emerging viral diseases in kidney transplant recipients. Rev Med Virol 2013, 23 : 50-69
35) Rosner MH, Edeani A, Yanagita M et al : Paraprotein-related kidney disease : Diagnosis and treating monoclonal gammopathy of renal significance. Clin J Am Soc Nephrology 2016, 11 : 2208-2287
36) Nasr SH, Satoskar A, Markowittz G et al : Proliferative glomerulonephritis with monoclonal IgG deposits. J Am Soc Nephrol 2009, 20 : 2055-2064
37) Merlini G : AL amyloidosis : from molecular mechanisms to target therapies. Hematology Am Soc Hematol Educ Program 2017, 2017 : 1-12
38) Manabe S, Iwasaki C, Hatano M et al : AL amyloidosis with non-amyloid forming monoclonal immunoglobulin deposition : a case mimicking AHL amyloidosis. BMC Nephrol 2018, 19 : 337
39) Alpers C, Kowalewska J : Fibrillary glomerulonephritis and immunotactoid glomerulopathy. J Am Soc Nephrol 2008, 19 : 34-37
40) Waldman M, Kopp JB : Parvovirus B19 and the kidney. Clin J Am Soc Nephrol 2007, 2 (Suppl 1) : S47-S56
41) Arakawa M : Idiopathic mesangio-degenerative glomerulopathy (Japanese). Jpn J Nephrol 1979, 21 : 914-915
42) Maynard S, Thadhani R : Pregnancy and the kidney. J Am Soc Nephrol 2009, 20 : 314-322
43) Saito T, Matsunaga A, Oikawa S : Impact of lipoprotein glomerulopathy on the relationship between lipids and renal diseases. Am J Kid Dis 2006, 47 : 199-211
44) 新田幸作, 政金生人, 花房規男ほか : わが国の慢性透析療法の現況. 透析会誌 2018, 51 : 699-766
45) Bright R : Reports of Medical Cases, selected with a view of illustrating the symptoms and cure of diseases by a reference to morbid anatomy. London : Richard Taylor for Longman, Rees, Orme, Brown, and Green, 1827
46) Bohle A, Ratschek M : The compensated and the decompensated form of benign nephrosclerosis. Pathol Res Pract 1982, 174 : 357-367
47) Kitiyakara C, Guzman NJ : Malignant hypertension and hypertensive emergencies. J Am Soc Nephrol 1998, 9 : 133-142
48) Jennette JC, Falk RJ, Bacon PA : 2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthritis Rheum 2013, 65 : 1-11
49) 日本腎臓学会 (編) : エビデンスに基づく急速進行性腎炎症候群 (RPGN) 診療ガイドライン, 東京医学社, 2014, 1-12
50) Haas M, Eustace JA : Immune complex deposits in ANCA-associated crescentic glomerulonephritis : a study of 126 cases. Kidney Int 2004, 65 : 2145-2152
51) McAdoo S, Pusey CD : Anti-Glomerular basement membrane disease. Clin J AM Soc Nephrol 2017, 12 : 1162-1172
52) Levy JB, Hammad T, Coulthart A et al : Clinical features and outcome of patients with both ANCA and anti-GBM antibodies. Kidney Int 2004, 66 : 1535-1540
53) D'Amico G, Fornasieri A : Cryoglobulinemic glomerulonephritis : A membranoproliferative glomerulonephritis induced by hepatitis C virus. Am J Kid Dis 1995, 25 : 361-369
54) Cacoub P, Comarmond C, Domont F et al : Cryoglobulinemia vasculitis. Am J Med 2015, 128 : 950-955
55) Ruperto N, Martini A, for the Pediatric Rheumatology International Trials Organisation (PRINTO) : Network in pediatric rheumatology : the example of the Pediatric Rheumatology International Trials Organisation. World J Pediatr 2008, 4 : 186-191
56) Davin JC, Coppo R : Henoch-Schonlein purpura in children. Nat Rev Nephrol 2014, 10 : 563-573
57) George JN, Nester CM : Syndromes of thrombotic microangiopathy. NEJM 2014, 371 : 654-666
58) Jokiranta TS : HUS and atypical HUS. Blood 2017, 129 : 2847-2856
59) Praga M, Gonzalez E : Acute interstitial nephritis. Kidney Int 2010, 77 : 956-961
60) Rosen S, Stillman I : Acute tubular necrosis is a syndrome of physiologic and pathophysiologic dissociation. Am J Soc Nephrol 2008, 19 : 871-875
61) Brodsky SV, Nasasdy T : Acute and chronic tubulointerstitial nephritis. in : Jennette JC, Olson JL, Silva FG et al (eds) : Heptinstall's Pathology of the Kidney, 7th ed, Wolters Kluwer, 2015, 1111-1165
62) Sinnamon KT, Coutney AE, Harron C et al : Tubulointerstitial nephritis and uveitis (TINU) syndrome : epidemiology, diagnosis and management. Nephrol Dial Transplant 2008, 2 : 112-116
63) Goebel U, Ketteritz R, Schneider W et al : The Protean Face of Renal Sarcoidosis. J Am Soc Nephrol 2001, 12 : 616-623
64) Jonsson R, Vogelsanga P, Volchenkov R et al : The complexity of Sjogren's syndrome : Novel aspects on pathogenesis. Immunol Lett 2011, 141 : 1-9
65) Kynakidis NC, Kapsogeorgou EK, Tzioufas AG : A comprehensive review of autoantibodies in primary Sjogren syndrome : clinical phenotypes and regulatory mechanisms. J Autoimmune 2014, 51 : 67-74
66) Hamano H, Kawa S, Horiuchi A : High serum IgG4 concentrations in patients with sclerosing pancreatitis. N Engl J Med 2001, 344 : 732-738
67) Kawano M, Saeki T, Nakashima H et al : Proposal for diagnostic criteria for IgG4-related kidney disease. Clin Exp Nephrol 2011, 15 : 615-626
68) Yamaguchi Y, Kanetsuna Y, Honda K et al : Characteristic tubulointerstitial nephritis in IgG4-related disease. Human Pathol 2012, 43 : 536-549
69) Dimopoulos MA, Terpos E, Chanan-Khan A et al : Renal impairment in patient with multiple myeloma : A consensus statement on behalf of the international myeloma working group. J Clin Oncol 2010, 28 : 4976-4984
70) Klootwijk ED, Reichold M, Unwin RJ et al : Renal Fanconi syndrome : taking a proximal look at the nephron. Nephrol Dial Transplant 2015, 30 : 1456-1460
71) Wolf MTF : Nephronophthisis and related syndromes. Curr Opin Pediatr 2015, 27 : 201-211
72) 井藤奈央子, 藤丸拓也, 長田道夫 : 髄質嚢胞性腎疾患研究の進歩. 日腎誌 2018, 60 : 543-552
73) Ghata J, Cowley BD Jr : Polycystic kidney disease. Compr Physiol 2017, 18 : 945-975
74) Guay-Woodford LM, Bissler JJ, Braun M et al : Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease : report of an international conference. J Pediatr 2014, 165 : 611-617
75) Winyard P, Chitty LS : Dysplastic kidneys. Semin Fetal Neonatal Med 2008, 13 : 142-151
76) Nozu K, Nakanishi K, Abe Y et al : A review of clinical characteristics and genetic backgrounds in Alport syndrome. Clin Exp Nephrol 2019, 23 : 158-168
77) Zarate Y, Hopkin RJ : Fabry's disease. Lancet 2008, 18 : 1427-1435
78) Chinnery PF : Mitochondrial disorders overview. GeneReviews [Internet] 2014, August 14
79) Kobayashi A, Goto Y, Nagata M et al : Granular swollen epithelial cells : a histological and diagnostic marker for mitochondrial nephropathy Am J Surg Pathol 2010, 34 : 262-270
80) Lusco MA, Chen Y, Cheng H et al : AJKD Atlas of Renal Pathology : Fibronectin glomerulopathy. Am J Kid Dis 2017, 70 : e21-e22
81) 日本臨床腎移植学会, 日本移植学会 : 腎移植臨床登録集計報告 (2018) 2017年実施症例の集計報告と追跡調査結果. 移植 2018, 53 : 89-108
82) Haas M, Loupy A, Lefaucheur C et al : The Banff 2017 Kidney Meeting Report : Revised diagnostic criteria for chronic active T cell mediated rejection, antibody-mediated rejection, and prospects for integrative endpoints for next-generation clinical trials. Am J Transplant 2018, 18 : 293-307
83) Naesens M, Kuypers DR, Sarwal M : Calcineurin inhibitor nephrotoxity. Clin J Am Soc Nephrol 2009, 4 : 481-508
84) Karuthu A, Blumberg E : Common infection in kidney transplant recipients. Clin J Am Soc Nephrol 2012, 7 : 2058-2070
85) De Keyzer K, Van Laecke S, Peeters P et al : Human Cytomegalovirus and Kidney Transplantation : A Clinician's Update. Am J Kidney Dis 2011, 58 : 118-126
86) Greena M, Michaels MG : Epstein Barr Virus Infection and Posttransplant Lymphoproliferative Disorder. Am J Transplant 2013, 13 : 41-54
P.958 掲載の参考文献
1) 国立がん研究センター がん情報サービス がん登録・統計 https://ganjoho.jp/reg_stat/statistics/stat/summary.html
2) Moch H, Ohashi R, Gandhi JS et al : Morphological clues to the appropriate recognition of hereditary renal neoplasms. Semin Diagn Pathol 2018, 35 : 184-192
3) Eble JN, Sauter G, Epstein JI et al : Tumours of the kidney. in : Eble JN, Sauter G, Epstein J et al (eds) : WHO Classification of Tumours. Pathology and Genetics. Tumours of the Urinary System and Male Genital Organs, 3rd ed, IARC Press, 2004, 9-87
4) 日本泌尿器科学会, 日本医学放射線学会, 日本病理学会 (編) : 腎癌取扱い規約, 第4版, 金原出版, 2011
5) Moch H, Martignoni G, Amin MB et al : Renal tumours. Introduction. in : Moch H, Humphery PA, Ulbight TM, et al (eds) : WHO Classification of Tumours of the Urinary System and Male Genital Organs, 4th ed, IARC Press, 2016, 14-17
6) Maher ER : Hereditary renal cell carcinoma syndromes : diagnosis, surveillance and management. World J Urol 2018, 36 : 1891-1898
7) Shen C, Kaelin WG Jr : The VHL/HIF axis in clear cell renal carcinoma. Semin Cancer Biol 2013, 23 : 18-25
8) Schmidt LS, Linehan WM : Molecular genetics and clinical features of Birt-Hogg-Dube syna drome. Nat Rev Urol 2015, 12 : 558-569
9) Courthod G, Tucci M, Di Maio M et al : Papillary renal cell carcinoma : A review of the current therapeutic landscape. Crit Rev Oncol Hematol 2015, 96 : 100-112
10) Ooi A : Advances in hereditary leiomyomatosis and renal cell carcinoma (HLRCC) research. Semin Cancer Biol 2019, S1044-579X (19) 30271-30278
11) Aghamir SMK, Heshmat R, Ebrahimi M et al : The Impact Of Succinate Dehydrogenase Gene (SDH) Mutations In Renal Cell Carcinoma (RCC) : A Systematic Review. Onco Targets Ther 2019, 12 : 7929-7940
12) Lam HC, Siroky BJ, Henske EP : Renal disease in tuberous sclerosis complex : pathogenesis and therapy. Nat Rev Nephrol 2018, 14 : 704-716
13) Hastie ND : Wilms' tumour 1 (WT1) in development, homeostasis and disease. Development 2017, 144 : 2862-2872
14) Maschietto M, Charlton J, Perotti D et al : The IGF signalling pathway in Wilms tumours--a report from the ENCCA Renal Tumours Biology-driven drug development workshop. Oncotarget 2014, 5 : 8014-8026
15) 一般社団法人日本病理学会 (編) : ゲノム診療用病理組織検体取扱い規程, 羊土社, 2019
16) 長嶋洋治, 谷口多美代, 古林直人ほか : 腎臓 (手術). 外科病理マニュアル, 病理と臨床 2008, 26 (臨増) : 277-282
17) Kuroda N, Tanaka A, Ohe C et al : Recent advances of immunohistochemistry for diagnosis of renal tumors. Pathol Int 2013, 63 : 381-390
18) 長嶋洋治, 鬼塚裕美, 澤田杏理ほか : 腎腫瘍の針生検病理組織診断. 診断病理 2016, 33 : 216-223
19) Collins J, Epstein JI : Prognostic significance of extensive necrosis in renal cell carcinoma. Hum Pathol 2017, 66 : 108-114
20) Delahunt B, Eble JN, Egevad L et al : Grading of renal cell carcinoma. Histopathology 2019, 74 : 4-17
21) Fuhrman SA, Lasky LC, Limas C : Prognostic significance in morphologic parameters in renal cell carcinoma. Am J Surg Pathol 1982, 6 : 656-663
22) Delahunt B, Cheville JC, Martignoni G et al : The International Society of Urological Pathology (ISUP) grading system for renal cell carcinoma and other prognostic parameters. Am J Surg Pathol 2013, 37 : 1490-1504
23) Hegemann M, Kroeger N, Stenzl A et al : Rare and changeable as a chameleon : paraneoplastic syndromes in renal cell carcinoma. World J Urol 2018, 36 : 849-854
24) Crestani A, Rossanese M, Calandriello M et al : Introduction to small renal tumours and prognostic indicators. Int J Surg 2016, 36 : 495-503
25) Sun M, Marconi L, Eisen T et al : Adjuvant Vascular Endothelial Growth Factor-targeted Therapy in Renal Cell Carcinoma : A Systematic Review and Pooled Analysis. Eur Urol 2018, 74 : 611-620
26) Porta C, Toscani I, Czarnecka AM et al : Immuno-oncology for renal cell carcinoma treatment : future perspectives for combinations and sequences with molecularly targeted agents. Expert Opin Biol Ther 2017, 17 : 151-162
27) Jonasch E, Gao J, Rathmell WK : Renal cell carcinoma. Version 2. BMJ 2014, 349 : g4797
28) Klatte T, Rossi SH, Stewart GD : Prognostic factors and prognostic models for renal cell carcinoma : a literature review. World J Urol 2018, 36 : 1943-1952
29) Ljungberg B, Bensalah K, Canfield S et al : EAU guidelines on renal cell carcinoma : 2014 update. Eur Urol 2015, 67 : 913-924
30) Varshney N, Kebede AA, Owusu-Dapaah H et al : A Review of von Hippel-Lindau Syndrome. J Kidney Cancer VHL 2017, 4 : 20-29
31) Maxwell PH, Wiesener MS, Chang GW et al : The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis. Nature 1999, 399 : 271-275
32) Chappell JC, Payne LB, Rathmell WK : Hypoxia, angiogenesis, and metabolism in the hereditary kidney cancers. J Clin Invest 2019, 129 : 442-451
33) Krieg M, Haas R, Brauch H et al : Up-regulation of hypoxia-inducible factors HIF-1alpha and HIF-2alpha under normoxic conditions in renal carcinoma cells by von Hippel-Lindau tumor suppressor gene loss of function. Oncogene 2000, 19 : 5435-5443
34) Al Tameemi W, Dale TP, Al-Jumaily RMK et al : Hypoxia-Modified Cancer Cell Metabolism. Front Cell Dev Biol 2019, 7 : 4
35) Tostain J, Li G, Gentil-Perret A et al : Carbonic anhydrase 9 in clear cell renal cell carcinoma : a marker for diagnosis, prognosis and treatment. Eur J Cancer 2010, 46 : 3141-3148
36) Piva F, Santoni M, Matrana MR et al : BAP1, PBRM1 and SETD2 in clear-cell renal cell carcinoma : molecular diagnostics and possible targets for personalized therapies. Expert Rev Mol Diagn 2015, 15 : 1201-1210
37) D'Avella C, Abbosh P, Pal SK et al : Mutations in renal cell carcinoma. Urol Oncol 2018, S1078-1439 : 30436-30438
38) Suzigan S, Lopez-Beltran A, Montironi R et al : Multilocular cystic renal cell carcinoma : a report of 45 cases of a kidney tumor of low malignant potential. Am J Clin Pathol 2006, 125 : 217-222
39) Tickoo SK, Reuter VE : Multilocular cystic clear cell renal cell neoplasm neoplasm of low malignant potential.in : Amin MB, Tickoo SK (eds) : Diagnostic Pathology Genitourinary, Elsevier, 2016, 64-67
40) von Teichman A, Comperat E, Behnke S et al : VHL mutations and dysregulation of pVHL- and PTEN-controlled pathways in multilocular cystic renal cell carcinoma. Mod Pathol 2011, 24 : 571-578
41) Cossu-Rocca P, Eble JN, Delahunt B et al : Renal mucinous tubular and spindle carcinoma lacks the gains of chromosomes 7 and 17 and losses of chromosome Y that are prevalent in papillary renal cell carcinoma. Mod Pathol 2006, 19 : 488-493
42) Kuroda N, Toi M, Hiroi M et al : Review of papillary renal cell carcinoma with focus on clinical and pathobiological aspects. Histol Histopathol 2003, 18 : 487-494
43) Tickoo SK, Reuter VE : Papillary renal cell carcinoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 80-89
44) Cheville JC, Lohse CM, Zincke H et al : Comparisons of outcome and prognostic features among histologic subtypes of renal cell carcinoma. Am J Surg Pathol 2003, 27 : 612-624
45) Delahunt B, Eble JN : Papillary Renal Cell Carcinoma : A Clinicopathologic and Immunohistochemical Study of 105 Tumors. Mod Pathol 1997, 10 : 537-544
46) Xia QY, Rao Q, Shen Q et al : Oncocytic papillary renal cell carcinoma : a clinicopathological study emphasizing distinct morphology, extended immunohistochemical profile and cytogenetic features. Int J Clin Exp Pathol 2013, 6 : 1392-1399
47) Kobayashi N, Matsuzaki O, Shirai S et al : Collecting duct carcinoma of the kidney : an immunohistochemical evaluation of the use of antibodies for differential diagnosis. Hum Pathol 2008, 39 : 1350-1359
48) Nagashima Y : Chromophobe renal cell carcinoma : clinical, pathological and molecular biological aspects. Pathol Int 2000, 50 : 872-878
49) Kuroda N, Toi M, Hiroi M et al : Review of chromophobe renal cell carcinoma with focus on clinical and pathobiological aspects. Histol Histopathol 2003, 18 : 165-171
50) Contractor H, Zariwala M, Bugert P et al : Mutation of the p53 tumour suppressor gene occurs preferentially in the chromophobe type of renal cell tumour. J Pathol 1997, 181 : 136-139
51) Ricketts CJ, De Cubas AA, Fan H et al : The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma. Cell Rep 2018, 23 : 313-326
52) Tickoo SK, Reuter VE : Chrmophobe renal cell carcinoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 90-97
53) Akhtar M, Tulbah A, Kardar AH et al : Sarcomatoid renal cell carcinoma : the chromophobe connection. Am J Surg Pathol 1997, 21 : 1188-1195
54) Sharma R, Kaushal V : Sarcomatoid chromophobe renal cell carcinoma : A rare entity with prognostic significance. J Cancer Res Ther 2015, 11 : 1030
55) Lohse CM, Gupta S, Cheville JC : Outcome prediction for patients with renal cell carcinoma. Semin Diagn Pathol 2015, 32 : 172-183
56) Lin TF, Lin WR, Chen M et al : Compare Fuhrman Nuclear and Chromophobe Tumor Grade on Chromophobe RCC. Open Med (Wars) 2019, 14 : 336-342
57) Taki A, Nakatani Y, Misugi K et al : Chromophobe renal cell carcinoma : an immunohistochemical study of 21 Japanese cases. Mod Pathol 1999, 12 : 310-317
58) Martignoni G, Pea M, Brunelli M et al : CD10 is expressed in a subset of chromophobe renal cell carcinomas. Mod Pathol 2004, 17 : 1455-1463
59) Mikami S, Kuroda N, Nagashima Y et al : Classification of solid renal tumor with oncocytic/eosinophilic cytoplasm : is hybrid oncocytic/chromophobe renal tumor a subtype of oncocytoma, chromophobe renal cell carcinoma, or a distinct tumor entity? Ann Transl Med 2019, 7 : S350
60) Furuya M, Hasumi H, Yao M et al : Birt-Hogg-Dube syndrome-associated renal cell carcinoma : Histopathological features and diagnostic conundrum. Cancer Sci 2020, 111 : 15-22
61) Tyrakis PA, Yurkovich ME, Sciacovelli M et al : Fumarate Hydratase Loss Causes Combined Respiratory Chain Defects. Cell Rep 2017, 21 : 1036-1047
62) Smith SC, Trpkov K, Chen YB et al : Tubulocystic carcinoma of the kidney with poorly differentiated foci : A frequent morphologic pattern of fumarate hydratase-deficient renal cell carcinoma. Am J Surg Pathol 2016, 40 : 1457-1472
63) Patel VM, Handler MZ, Schwartz RA et al : Hereditary leiomyomatosis and renal cell cancer syndrome : An update and review. J Am Acad Dermatol 2017, 77 : 149-158
64) Tickoo SK, Reuter VE : Hereditary leiomyomatosis renal cell carcinoma syndrome. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 20-23
65) Ulamec M, Skenderi F, Zhou M et al : Molecular genetic alterations in renal cell carcinomas with tubulocystic pattern : Tubulocystic renal cell carcinoma, tubulocystic renal cell carcinoma with heterogenous component and familial leiomyomatosis-associated renal cell carcinoma. Clinicopathologic and molecular genetic analysis of 15 Cases. Appl Immunohistochem Mol Morphol 2016, 24 : 521-530
66) Tickoo SK, Reuter VE : Collecting duct carcinoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016. 98-104
67) Tokuda N, Naito S, Matsuzaki O et al : Japanese Society of Renal Cancer. Collecting duct (Bellini duct) renal cell carcinoma : a nationwide survey in Japan. J Urol 2006, 176 : 40-43
68) Singh JA, Ohe C, Smith SC : High grade infiltrative adenocarcinomas of renal cell origin : New insights into classification, morphology, and molecular pathogenesis. Pathol Int 2018, 68 : 265-277
69) Sugawara E, Togashi Y, Kuroda N et al : Identification of anaplastic lymphoma kinase fusions in renal cancer : large-scale immunohistochemical screening by the intercalated antibody-enhanced polymer method. Cancer 2012, 118 : 4427-4736
70) Argani P : MiT family translocation renal cell carcinoma. Semin Diagn Pathol 2015, 32 : 103-113
71) Kato I, Furuya M, Baba M et al : RBM10-TFE3 renal cell carcinoma characterised by paracentric inversion with consistent closely split signals in break-apart fluorescence in-situ hybridisation : study of 10 cases and a literature review. Histopathology 2019, 75 : 254-265
72) Tickoo SK, Reuter VE : Succinate dehydrogenase complex deficiency syndrome. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 28-31
73) Tickoo SK, Reuter VE : Mucinous tubular and spindle cell carcinoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 118-123
74) Nathany S, Monappa V : Mucinous tubular and spindle cell carcinoma : A review of histopathology and clinical and prognostic implications. Arch Pathol Lab Med 2019. doi : 10.5858/arpa.2017-0506-RS
75) Tickoo SK, Reuter VE : Tubulocystic carcinoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 124-127
76) Tickoo SK, de Peralta-Venturina MN, Harik LR et al : Spectrum of epithelial neoplasms in endstage renal disease : an experience from 66 tumor-bearing kidneys with emphasis on histologic patterns distinct from those in sporadic adult renal neoplasia. Am J Surg Pathol 2006, 30 : 141-153
77) Ishikawa I, Kovacs G : High incidence of papillary renal cell tumours in patients on chronic haemodialysis. Histopathology 1993, 22 : 135-139
78) Tickoo SK, Reuter VE : Acquired cystic disease-associated renal cell carcinoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 132-138
79) Tickoo SK, Reuter VE : Clear cell papillary renal cell carcinoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 72-79
80) Batavia AA, Schraml P, Moch H : Clear cell renal cell carcinoma with wild-type on Hippel-Lindau gene : a non-existent or new tumour entity? Histopathology 2019, 74 : 60-67
81) Tickoo SK, Reuter VE : Thyroid-like follicular carcinoma of the kidney. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 128-131
82) Tickoo SK, Reuter VE : Papillary adenoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 44-47
83) Van Poppel H, Nilsson S, Algaba F et al : Precancerous lesions in the kidney. Scand J Urol Nephrol 2000, 205 : 136-165
84) Tickoo SK, Reuter VE : Renal oncocytoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 48-53
85) Brimo F, Epstein JI : Selected common diagnostic problems in urologic pathology : perspectives from a large consult service in genitourinary pathology. Arch Pathol Lab Med 2012, 136 : 360-371
86) 日本病理学会小児腫瘍組織分類委員会 (編) : 小児腫瘍組織カラーアトラス 第4巻 小児腎腫瘍, 金原出版, 2008
87) Riccio A, Sparago A, Verde G et al : Inherited and sporadic epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor. Endocr Dev 2009, 14 : 1-9
88) Pavlick D, Schrock AB, Malicki D et al : Identification of NTRK fusions in pediatric mesenchymal tumors. Pediatr Blood Cancer 2017, 64. doi : 10.1002/pbc.26433
89) Argani P, Ladanyi M : Recent advances in pediatric renal neoplasia. Adv Anat Pathol 2003, 10 : 243-260
90) Uddin N, Minhas K, Abdul-Ghafar J et al : Expression of cyclin D1 in clear cell sarcoma of kidney. Is it useful in differentiating it from its histological mimics? Diagn Pathol 2019, 14 : 13
91) Aw SJ, Chang KTE : Clear Cell Sarcoma of the Kidney. Arch Pathol Lab Med 2019, 143 : 1022-1026
92) Wong MK, Ng CCY, Kuick CH et al : Clear cell sarcomas of the kidney are characterised by BCOR gene abnormalities, including exon 15 internal tandem duplications and BCOR-CCNB3 gene fusion. Histopathology 2018, 72 : 320-329
93) Pawel BR : SMARCB1-deficient Tumors of Childhood : A Practical Guide. Pediatr Dev Pathol 2018, 21 : 6-28
94) Tamboli P, Ro JY, Amin MB et al : Benign tumors and tumor-like lesions of the adult kidney. Part II : Benign mesenchymal and mixed neoplasms, and tumor-like lesions. Adv Anat Pathol 2000, 7 : 47-66
95) Tickoo SK, Reuter VE : Metanephric adenoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 146-151
96) Nagashima Y, Arai N, Tanaka Y et al : Two cases of a renal epithelial tumour resembling immature nephron. Virchows Arch A Pathol Anat Histopathol 1991, 418 : 77-81
97) Wataya-Kaneda M, Uemura M, Fujita K et al : Tuberous sclerosis complex : Recent advances in manifestations and therapy. Int J Urol 2017, 24 : 681-691
98) McEneaney LJ, Tee AR : Finding a cure for tuberous sclerosis complex : From genetics through to targeted drug therapies. Adv Genet 2019, 103 : 91-118
99) Wei J, Li Y, Wen Y et al : Renal angiomyolipoma with epithelial cysts : a rare entity and review of literature. Int J Clin Exp Pathol 2015, 8 : 11760-11765
100) Ackerman TE, Levi CS, Lindsay DJ et al : Angiomyolipoma with lymph node involvement. Can Assoc Radiol J 1994, 45 : 52-55
101) Tickoo SK, Reuter VE : Epithelioid angiomyolipoma. in : Amin MB, Tickoo SK : Diagnostic Pathology : Genitourinary, Elsevier, 2016, 178-183
102) Nese N, Martignoni G, Fletcher CD et al : Pure epithelioid PEComas (so-called epithelioid angiomyolipoma) of the kidney : A clinicopathologic study of 41 cases : detailed assessment of morphology and risk stratification. Am J Surg Pathol 2011, 35 : 161-176
103) Kuroda N, Gotoda H, Ohe C et al : Review of juxtaglomerular cell tumor with focus on pathobiological aspect. Diagn Pathol 2011, 6 : 80
104) Duan X, Bruneval P, Hammadeh R et al : Metastatic juxtaglomerular cell tumor in a 52-yearold man. Am J Surg Pathol 2004, 28 : 1098-1102
105) Montironi R, Mazzucchelli R, Lopez-Beltran A et al : Cystic nephroma and mixed epithelial and stromal tumour of the kidney : opposite ends of the spectrum of the same entity? Eur Urol 2008, 54 : 1237-1246
106) Calio A, Eble JN, Grignon DJ et al : Mixed Epithelial and Stromal Tumor of the Kidney : A Clinicopathologic Study of 53 Cases. Am J Surg Pathol 2016, 40 : 1538-1549
107) Jung SJ, Shen SS, Tran T et al : Mixed epithelial and stromal tumor of kidney with malignant transformation : report of two cases and review of literature. Hum Pathol 2008, 39 : 463-468
P.992 掲載の参考文献
1) Didier RA, Chow JS, Kwatra NS et al : The duplicated collecting system of the urinary tract : embryology, imaging appearances and clinical considerations. Pediatr Radiol 2017, 47 : 1526-1538
2) Timberlake MD, Corbett ST : Minimally invasive techniques for management of the ureterocele and ectopic ureter : upper tract versus lower tract approach. Urol Clin North Am 2015, 42 : 61-76
3) Scales CD, Jr., Smith AC, Hanley JM et al : Prevalence of kidney stones in the United States. Eur Urol 2012, 62 : 160-165
4) Moch H, Humphrey PA, Ulbright TM et al : Tumours of the urinary tract. In : World Health Organization classification of tumours of the urinary system and male genital organs, 4th ed., IARC Press, 2016
5) Siegel RL, Miller KD, Jemal A : Cancer statistics, 2019. CA Cancer J Clin 2019, 69 : 7-34
6) Roupret M, Yates DR, Comperat E et al : Upper urinary tract urothelial cell carcinomas and other urological malignancies involved in the hereditary nonpolyposis colorectal cancer (lynch syndrome) tumor spectrum. Eur Urol 2008, 54 : 1226-1236
7) Roupret M, Babjuk M, Comperat E et al : European Association of Urology Guidelines on Upper Urinary Tract Urothelial Carcinoma : 2017 Update. Eur Urol 2018, 73 : 111-122
8) Amin MB, Edge SB, Greene FL et al : AJCC Cancer Staging Manual, 8th ed., Springer, 2017
9) Brierley JD, Gospodarowicz MK, Wittekind C : TNM Classification of Malignant Tumours, 8th ed., Wiley, 2017
10) Paner GP, Montironi R, Amin MB : Challenges in pathologic staging of bladder cancer : proposals for fresh approaches of assessing pathologic stage in light of recent studies and observations pertaining to bladder histoanatomic variances. Adv Anat Pathol 2017, 24 : 113-127
11) Snyder CL : Current management of umbilical abnormalities and related anomalies. Semin Pediatr Surg 2007, 16 : 41-49
12) Yiee J, Wilcox D : Abnormalities of the fetal bladder. Semin Fetal Neonatal Med 2008, 13 : 164-170
13) Tamas EF, Stephenson AJ, Campbell SC et al : Histopathologic features and clinical outcomes in 71 cases of bladder diverticula. Arch Pathol Lab Med 2009, 133 : 791-796
14) Smeulders N, Woodhouse CR : Neoplasia in adult exstrophy patients. BJU Int 2001, 87 : 623-628
15) Garat JM, Angerri O, Caffaratti J et al : Primary congenital bladder diverticula in children. Urology 2007, 70 : 984-988
16) Idrees MT, Alexander RE, Kum JB et al : The spectrum of histopathologic findings in vesical diverticulum : implications for pathogenesis and staging. Hum Pathol 2013, 44 : 1223-1232
17) Voskuilen CS, Seiler R, Rink M et al : Urothelial carcinoma in bladder diverticula : a multicenter analysis of characteristics and clinical outcomes. Eur Urol Focus 2018 Dec 14. [Epub ahead of print]
18) Tirzaman O, Wahner-Roedler DL, Malek RS et al : Primary localized amyloidosis of the urinary bladder : a case series of 31 patients. Mayo Clin Proc 2000, 75 : 1264-1268
19) Clouston D, Lawrentschuk N : Metaplastic conditions of the bladder. BJU Int 2013, 112 (Suppl 2) : 27-31
20) Lane Z, Epstein JI : Polypoid/papillary cystitis : a series of 41 cases misdiagnosed as papillary urothelial neoplasia. Am J Surg Pathol 2008, 32 : 758-764
21) Babjuk M, Bohle A, Burger M et al : EAU guidelines on non-muscle-invasive urothelial carcinoma of the bladder : update 2016. Eur Urol 2017, 71 : 447-61
22) Popescu OE, Landas SK, Haas GP : The spectrum of eosinophilic cystitis in males : case series and literature review. Arch Pathol Lab Med 2009, 133 : 289-294
23) Matz EL, Hsieh MH : Review of advances in uroprotective agents for cyclophosphamide- and ifosfamide-induced hemorrhagic cystitis. Urology 2017, 10 : 16-19
24) Mani J, Jin N, Schmitt M : Cellular immunotherapy for patients with reactivation of JC and BK polyomaviruses after transplantation. Cytotherapy 2014, 16 : 1325-1335
25) Mazal PR, Schaufler R, Altenhuber-Muller R et al : Derivation of nephrogenic adenomas from renal tubular cells in kidney-transplant recipients. N Engl J Med 2002, 347 : 653-659
26) Philippou P, Shabbir M, Ralph DJ et al : Genital lichen sclerosus/balanitis xerotica obliterans in men with penile carcinoma : a critical analysis. BJU Int 2013, 111 : 970-976
27) Spagnolo DV, Waring PM : Bladder granulomata after bladder surgery. Am J Clin Pathol 1986, 86 : 430-437
28) Tsuzuki T, Epstein JI : Fibroepithelial polyp of the lower urinary tract in adults. Am J Surg Pathol 2005, 29 : 460-466
29) Burger M, Catto JW, Dalbagni G et al : Epidemiology and risk factors of urothelial bladder cancer. Eur Urol 2013, 63 : 234-241
30) Bedwani R, Renganathan E, El Kwhsky F et al : Schistosomiasis and the risk of bladder cancer in Alexandria, Egypt. Br J Cancer 1998, 77 : 1186-1189
31) Li N, Yang L, Zhang Y et al : Human papillomavirus infection and bladder cancer risk : a meta-analysis. J Infect Dis 2011, 204 : 217-223
32) Ho CH, Sung KC, Lim SW et al : Chronic indwelling urinary catheter increase the risk of bladder cancer, even in patients without spinal cord injury. Medicine (Baltimore) 2015, 94 : e1736
33) Nieder AM, Porter MP, Soloway MS : Radiation therapy for prostate cancer increases subsequent risk of bladder and rectal cancer : a population based cohort study. J Urol 2008, 180 : 2005-2009
34) Skeldon SC, Semotiuk K, Aronson M et al : Patients with Lynch syndrome mismatch repair gene mutations are at higher risk for not only upper tract urothelial cancer but also bladder cancer. Eur Urol 2013, 63 : 379-385
35) Kamat AM, Hahn NM, Efstathiou JA et al : Bladder cancer. Lancet 2016, 388 : 2796-2810
36) 日本泌尿器科学会, 日本病理学会, 日本医学放射線学会 : 腎盂・尿管・膀胱癌取扱い規約, 第1版, 金原出版, 2011
37) Hedegaard J, Lamy P, Nordentoft I et al : Comprehensive Transcriptional Analysis of Early-Stage Urothelial Carcinoma. Cancer Cell 2016, 30 : 27-42
38) Moschini M, D'Andrea D, Korn S et al : Characteristics and clinical significance of histological variants of bladder cancer. Nat Rev Urol 2017, 14 : 651-668
39) Lopez-Beltran A, Henriques V, Montironi R et al : Variants and new entities of bladder cancer. Histopathology 2019, 74 : 77-96
40) Robertson AG, Kim J, Al-Ahmadie H et al : Comprehensive Molecular Characterization of Muscle-Invasive Bladder Cancer. Cell 2017, 171 : 540-556
41) Amin MB, Smith SC, Reuter VE et al : Update for the practicing pathologist : The International Consultation On Urologic Disease-European association of urology consultation on bladder cancer. Mod Pathol 2015, 28 : 612-630
42) Amin MB, Trpkov K, Lopez-Beltran A et al : Best practices recommendations in the application of immunohistochemistry in the bladder lesions : report from the International Society of Urologic Pathology consensus conference. Am J Surg Pathol 2014, 38 : e20-e34
43) Salem HK, Mahfouz S : Changing patterns (age, incidence, and pathologic types) of schistosoma-associated bladder cancer in Egypt in the past decade. Urology 2012, 79 : 379-383
44) Martucci VL, Lorenzo ZG, Weintraub M et al : Association of urinary bladder paragangliomas with germline mutations in the SDHB and VHL genes. Urol Oncol 2015, 33 : 167
45) Tsuzuki T, Magi-Galluzzi C, Epstein JI : ALK-1 expression in inflammatory myofibroblastic tumor of the urinary bladder. Am J Surg Pathol 2004, 28 : 1609-1614
46) Montgomery EA, Shuster DD, Burkart AL et al : Inflammatory myofibroblastic tumors of the urinary tract : a clinicopathologic study of 46 cases, including a malignant example inflammatory fibrosarcoma and a subset associated with highgrade urothelial carcinoma. Am J Surg Pathol 2006, 30 : 1502-1512
47) Wu IB, Schwartz RA : Reiter's syndrome : the classic triad and more. J Am Acad Dermatol 2008, 59 : 113-121
48) Sui W, RoyChoudhury A, Wenske S et al : Outcomes and Prognostic Factors of Primary Urethral Cancer. Urology 2017, 100 : 180-186
49) Zhang M, Adeniran AJ, Vikram R et al : Carcinoma of the urethra. Hum Pathol 2018, 72 : 35-44
50) Clouston D, Hall A, Lawrentschuk N : Penile lichen sclerosus (balanitis xerotica obliterans). BJU Int 2011, 108 (Suppl 2) : 14-19
51) Velazquez EF, Cubilla AL : Lichen sclerosus in 68 patients with squamous cell carcinoma of the penis : frequent atypias and correlation with special carcinoma variants suggests a precancerous role. Am J Surg Pathol 2003, 27 : 1448-1453
52) Ingles DJ, Pierce Campbell CM, Messina JA et al : Human papillomavirus virus (HPV) genotype- and age-specific analyses of external genital lesions among men in the HPV Infection in Men (HIM) Study. J Infect Dis 2015, 211 : 1060-1067
53) Taylor FL, Levine LA : Peyronie's Disease. Urol Clin North Am 2007, 34 : 517-534
54) Olesen TB, Sand FL, Rasmussen CL et al : Prevalence of human papillomavirus DNA and p16 (INK4a) in penile cancer and penile intraepithelial neoplasia : a systematic review and meta-analysis. Lancet Oncol 2019, 20 : 145-158
55) Velazquez EF, Ayala G, Liu H et al : Histologic grade and perineural invasion are more important than tumor thickness as predictor of nodal metastasis in penile squamous cell carcinoma invading 5 to 10 mm. Am J Surg Pathol 2008, 32 : 974-979
56) Joshi SS, Handorf E, Strauss D et al : Treatment trends and outcomes for patients with lymph node-positive cancer of the penis. JAMA Oncol 2018, 4 : 643-649
57) Hakenberg OW, Comperat EM, Minhas S et al : EAU guidelines on penile cancer : 2014 update. Eur Urol 2015, 67 : 142-150
58) O'Brien JS, Perera M, Manning T et al : Penile cancer : contemporary lymph node management. J Urol 2017, 197 : 1387-1395
P.1026 掲載の参考文献
1) Sadler TW : Langman's Medical Embryology, fourteenth edition, Wolters Kluwer, 2019, 267-283
2) Nistal M, Paniagua R, Gonzalez-Peramato P : Chapter 12, Nonneoplastic disease of the testis. In Cheng L, MacLennan GT, Bostwick DG ed., Urologic Surgical Pathology, 4th ed., Elsevier 2019, 549-730
3) 森永正二郎 : 精巣と精巣付属器. 病理診断に直結した組織学. 病理と臨床 (臨時増刊号) 2017, 35 : 305-319
5) Ono M, Harley VR : Disorders of sex development : new genes, new concepts. Nat Rev Endocrinol 2013, 9 : 79-91
6) Magers MJ, Udager AM, Chinnaiyan AM et al : Comprehensive immunophenotypic characterization of adult and fetal testes, the excretory duct system, and testicular and epididymal appendages. Appl Immunohistochem Mol Morphol 2016, 24 : e50-e68
7) Osterballe L, Clasen-Linde E, Cortes D et al : The diagnostic impact of testicular biopsies for intratubular germ cell neoplasia in cryptorchid boys and the subsequent risk of testicular cancer in men with prepubertal surgery for syndromic or non-syndromic cryptorchidism. J Pediatr Surg 2017, 52 : 587-592
8) Koni A, Ozseker HS, Arpali E et al : Histopathological evaluation of orchiectomy specimens in 51 late postpubertal men with unilateral cryptorchidism. J Urol 2014, 192 : 1183-1188
9) 中島信一, 緒方勤 : 性分化疾患の分類. 臨床泌尿器科 2017, 71 : 759-763
10) Lepais L, Morel Y, Mouriquand P et al : A novel morphological approach to gonads in disorders of sex development. Mod Pathol 2016, 29 : 1399-1414
11) Wikstrom AM, Dunkel L : Klinefelter syndrome. Best Pract Res Clin Endocrinol Metab 2011, 25 : 239-250
12) Ulbright TM, Young RH : Gonadoblastoma and selected other aspects of gonadal pathology in young patients with disorders of sex development. Semin Diagn Pathol 2014, 31 : 427-440
13) Nishina-Uchida N, Fukuzawa R, Ishii T et al : The distribution and cellular lineages of XX and XY cells in gonads associated with ovotesticular disorder of sexual development. Sex Dev 2016, 10 : 185-190
14) Shukla GC, Plaga AR, Shankar E et al : Androgen receptor-related diseases : what do we know? Andrology 2016, 4 : 366-381
15) Cools M, Looijenga L : Update on the pathophysiology and risk factors for the development of malignant testicular germ cell tumors in complete androgen insensitivity syndrome. Sex Dev 2017, 11 : 175-181
16) Olesen IA, Andersson AM, Aksglaede L et al : Clinical, genetic, biochemical, and testicular biopsy findings among 1, 213 men evaluated for infertility. Fertil Steril 2017, 107 : 74-82
17) Abdel Raheem A, Garaffa G, Rushwan N et al : Testicular histopathology as a predictor of a positive sperm retrieval in men with non-obstructive azoospermia. BJU Int 2013, 111 : 492-499
19) Nistal M, Paniagua R, Gonzalez-Peramato P et al : Perspectives in pediatric pathology, chapter 19. Testicular torsion, testicular appendix torsion, and other forms of testicular infarction. Pediatr Dev Pathol 2016, 19 : 345-359
20) Howitt BE, Berney DM : Tumors of the testis : morphologic features and molecular alterations. Surg Pathol Clin 2015, 8 : 687-716
21) Lobo J, Costa AL, Vilela-Salgueiro B et al : Testicular germ cell tumors : revisiting a series in light of the new WHO classification and AJCC staging systems, focusing on challenges for pathologists. Hum Pathol 2018, 82 : 113-124
22) Tarrant WP, Czerniak BA, Guo CC : Relationship between primary and metastatic testicular germ cell tumors : a clinicopathologic analysis of 100 cases. Hum Pathol 2013, 44 : 2220-2226
23) TNM悪性腫瘍の分類, 第8版, 日本語版, 金原出版, 2017, 195-198
24) AJCC Cancer Staging Manual, Eighth Edition, Springer, 2017, 727-735
25) Ulbright TM, Tickoo SK, Berney DM et al : Best practices recommendations in the application of immunohistochemistry in testicular tumors : report from the International Society of Urological Pathology consensus conference. Am J Surg Pathol 2014, 38 : e50-e59
26) Cheng L, Lyu B, Roth LM : Perspectives on testicular germ cell neoplasms. Hum Pathol 2017, 59 : 10-25
27) Miettinen M, Wang Z, McCue PA et al : SALL4 expression in germ cell and non-germ cell tumors : a systematic immunohistochemical study of 3215 cases. Am J Surg Pathol 2014, 38 : 410-420
28) 森永正二郎 : 精巣腫瘍の臨床病理学的問題点. 病理と臨床 2012, 30 : 1086-1101
29) Moch H, Humphrey PA, Ulbright TM et al : WHO Classification of Tumours of the Urinary System and Male Genital Organs, 4th ed, IARC, 2016
30) Williamson SR, Delahunt B, Magi-Galluzzi C et al : The World Health Organization 2016 classification of testicular germ cell tumours : a review and update from the International Society of Urological Pathology Testis Consultation Panel. Histopathology 2017, 70 : 335-346
31) Magers MJ, Kao CS, Cole CD et al : "Somatic-type" malignancies arising from testicular germ cell tumors : a clinicopathologic study of 124 cases with emphasis on glandular tumors supporting frequent yolk sac tumor origin. Am J Surg Pathol 2014, 38 : 1396-1409
32) Howitt BE, Magers MJ, Rice KR et al : Many postchemotherapy sarcomatous tumors in patients with testicular germ cell tumors are sarcomatoid yolk sac tumors : a study of 33 cases. Am J Surg Pathol 2015, 39 : 251-259
33) Mikuz G, Colecchia M : Teratoma with somatic-type malignant components of the testis. A review and an update. Virchows Arch 2012, 461 : 27-32
34) Kum JB, Ulbright TM, Williamson SR et al : Molecular genetic evidence supporting the origin of somatic-type malignancy and teratoma from the same progenitor cell. Am J Surg Pathol 1012, 36 : 1849-1856
35) Ulbright TM, Hattab EM, Zhang S et al : Primitive neuroectodermal tumors in patients with testicular germ cell tumors usually resemble pediatric-type central nervous system embryonal neoplasms and lack chromosome 22 rearrangements. Mod Pathol 2010, 23 : 972-980
36) Emerson RE, Ulbright TM, Zhang S et al : Nephroblastoma arising in a germ cell tumor of testicular origin. Am J Surg Pathol 2004, 28 : 687-692
37) Clevenger JA, Foster RS, Ulbright TM : Differentiated rhabdomyomatous tumors after chemotherapy for metastatic testicular germ-cell tumors : a clinicopathological study of seven cases mandating separation from rhabdomyosarcoma. Mod Pathol 2009, 22 : 1361-1366
38) Alvarado-Cabrero I, Hernandez-Toriz N, Paner GP : Clinicopathologic analysis of choriocarcinoma as a pure or predominant component of germ cell tumor of the testis. Am J Surg Pathol 2014, 38 : 111-118
39) Idrees MT, Kao CS, Epstein JI et al : Nonchoriocarcinomatous trophoblastic tumors of the testis : The widening spectrum of trophoblastic neoplasia. Am J Surg Pathol 2015, 39 : 1468-1478
40) Stall JN, Young RH : Polyembryoma of the testis : a report of two cases dominant within mixed germ cell tumors and review of gonadal polyembryomas. Mod Pathol 2017, 30 : 908-918
41) Zamecnik M, Sultani K : Diffuse embryoma with intratubular germ-cell neoplasia. Histopathology 2004, 45 : 427429
42) Balzer BL, Ulbright TM : Spontaneous regression of testicular germ cell tumors : an analysis of 42 cases. Am J Surg Pathol 2006, 30 : 858-865
43) 日本泌尿器科学会・日本病理学会・日本医学放射線学会・日本臨床腫瘍学会編 : 精巣腫瘍取り扱い規約, 第4版, 金原出版, 2018
44) Ulbright TM, Young RH : Testicular and paratesticular tumors and tumor-like lesions in the first 2 decades. Semin Diagn Pathol 2014, 31 : 323-381
45) Cornejo KM, Frazier L, Lee RS et al : Yolk sac tumor of the testis in infants and children : A clinicopathologic analysis of 33 cases. Am J Surg Pathol 2015, 39 : 1121-1131
46) Zhang C, Berney DM, Hirsch MS et al : Evidence supporting the existence of benign teratomas of the postpubertal testis : a clinical, histopathologic, and molecular genetic analysis of 25 cases. Am J Surg Pathol 2013, 37 : 827-835
47) Umar SA, MacLennan GT : Epidermoid cyst of the testis. J Urol 2008, 180 : 335
48) Younger C, Ulbright TM, Zhang S et al : Molecular evidence supporting the neoplastic nature of some epidermoid cysts of the testis. Arch Pathol Lab Med 2003, 127 : 858-860
49) Wang WP, Guo C, Berney DM et al : Primary carcinoid tumors of the testis : a clinicopathologic study of 29 cases. Am J Surg Pathol 2010, 34 : 519-524
50) Abbosh PH, Zhang S, Maclennan GT et al : Germ cell origin of testicular carcinoid tumors. Clin Cancer Res 2008, 14 : 1393-1396
51) Giannoulatou E, Maher GJ, Ding Z et al : Whole-genome sequencing of spermatocytic tumors provides insights into the mutational processes operating in the male germline. PLoS One 2017, 12 : e0178169
52) Hu R, Ulbright TM, Young RH : Spermatocytic seminoma : A report of 85 cases emphasizing its morphologic spectrum including some aspects not widely known. Am J Surg Pathol 2019, 43 : 1-11
53) Roth LM, Lyu B, Cheng L : Perspectives on testicular sex cord-stromal tumors and those composed of both germ cells and sex cord-stromal derivatives with a comparison to corresponding ovarian neoplasms. Hum Pathol 2017, 65 : 1-14
54) Heer R, Jackson MJ, El-Sherif A et al : Twenty-nine Leydig cell tumors : histological features, outcomes and implications for management. Int J Urol 2010, 17 : 886-889
55) Kao CS, Kum JB, Idrees MT et al : Sclerosing Sertoli cell tumor of the testis : a clinicopathologic study of 20 cases. Am J Surg Pathol 2014, 38 : 510-517
56) Mesa H, Gilles S, Datta MW et al : Comparative immunomorphology of testicular Sertoli and sertoliform tumors. Hum Pathol 2017, 61 : 181-189
57) Zhang C, Ulbright TM : Nuclear localization of β-catenin in sertoli cell tumors and other sex cord-stromal tumors of the testis : An immunohistochemical study of 87 cases. Am J Surg Pathol 2015, 39 : 1390-1394
58) Henley JD, Young RH, Ulbright TM : Malignant Sertoli cell tumors of the testis. A study of 13 examples of a neoplasm frequently misinterpreted as seminoma. Am J Surg Pathol 2002, 26 : 541-550
59) Petersson F, Bulimbasic S, Sima R et al : Large cell calcifying Sertoli cell tumor : a clinicopathologic study of 1 malignant and 3 benign tumors using histomorphology, immunohistochemistry, ultrastructure, comparative genomic hybridization, and polymerase chain reaction analysis of the PRKAR1A gene. Hum Pathol 2010, 41 : 552-559
60) Cornejo KM, Young RH : Adult granulosa cell tumors of the testis : a report of 32 cases. Am J Surg Pathol 2014, 38 : 1242-1250
61) Hes O1, Vanecek T, Petersson F et al : Mutational analysis (c.402C > G) of the FOXL2 gene and immunohistochemical expression of the FOXL2 protein in testicular adult type granulosa cell tumors and incompletely differentiated sex cord stromal tumors. Appl Immunohistochem Mol Morphol 2011, 19 : 347-351
62) Kao CS, Cornejo KM, Ulbright TM et al : Juvenile granulosa cell tumors of the testis : a clinicopathologic study of 70 cases with emphasis on its wide morphologic spectrum. Am J Surg Pathol 2015, 39 : 1159-1169
63) Kao CS, Ulbright TM : Myoid gonadal stromal tumor : a clinicopathologic study of three cases of a distinctive testicular tumor. Am J Clin Pathol 2014, 142 : 675-682
64) Burger T, Schildhaus HU, Inniger R et al : Ovarian-type epithelial tumours of the testis : immunohistochemical and molecular analysis of two serous borderline tumours of the testis. Diagn Pathol 2015, 10 : 118
65) Gwiti P, Vereczkey I, Cundell D et al : The mutational frequency of BRAF and KRAS in lowgrade serous testicular neoplasms-a case series. Histopathology 2017, 71 : 686-692
66) Cheah CY, Wirth A, Seymour JF : Primary testicular lymphoma. Blood 2014, 123 : 486-493
67) Amin MB : Selected other problematic testicular and paratesticular lesions : rete testis neoplasms and pseudotumors, mesothelial lesions and secondary tumors. Mod Pathol 2005, 18 Suppl 2 : S131-S145
68) Ulbright TM, Young RH : Metastatic carcinoma to the testis : a clinicopathologic analysis of 26 nonincidental cases with emphasis on deceptive features. Am J Surg Pathol 2008, 32 : 1683-1693
69) Algaba F, Mikuz G, Boccon-Gibod L et al : Pseudoneoplastic lesions of the testis and paratesticular structures. Virchows Arch 2007, 451 : 987-997
70) Hernandez-Rodriguez J, Tan CD, Koening CL et al : Testicular vasculitis : findings differentiating isolated disease from systemic disease in 72 patients. Medicine (Baltimore) 2012, 91 : 75-85
71) Cox R, Vang R, Epstein JI : Papillary cystadenoma of the epididymis and broad ligament : morphologic and immunohistochemical overlap with clear cell papillary renal cell carcinoma. Am J Surg Pathol 2014, 38 : 713-718
72) Goode B, Joseph NM, Stevers M et al : Adenomatoid tumors of the male and female genital tract are defined by TRAF7 mutations that drive aberrant NF-κB pathway activation. Mod Pathol 2018, 31 : 660-673
73) Skinnider BF, Young RH : Infarcted adenomatoid tumor : a report of five cases of a facet of a benign neoplasm that may cause diagnostic difficulty. Am J Surg Pathol 2004, 28 : 77-83
74) Sedig L, Geiger J, Mody R Jet al : Paratesticular desmoplastic small round cell tumors : A case report and review of the literature. Pediatr Blood Cancer 2017, 64 : e26631
P.1061 掲載の参考文献
1) 日本泌尿器科学会, 日本病理学会, 日本医学放射線学会編 : 前立腺癌取扱い規約, 第4版, 金原出版, 2010, 70-71
2) Stillwell TJ, Engen DE, Farrow GM : The clinical spectrum of granulomatous prostatitis : a report of 200 cases. J Urol 1987, 138 : 320-323
3) Hauck EW, Battmann A, Schmelz HU et al : Giant multilocular cystadenoma of the prostate : a rare differential diagnosis of benign prostatic hyperplasia. Urol Int 2004, 73 : 365-369
5) Takahashi H, Epstein JI, Wakui S et al : Differences in prostate cancer grade, stage, and location in radical prostatectomy specimens from United States and Japan. Prostate 2014, 74 : 321-325
6) Ro JY, Ayala AG, Ordonez NG et al : Intraluminal crystalloids in prostatic adenocarcinoma. Immunohistochemical, electron microscopic, and x-ray microanalytic studies. Cancer 1986, 57 : 2397-2407
7) Epstein JI : Diagnostic criteria of limited adenocarcinoma of the prostate on needle biopsy. Hum Pathol 1995, 26 : 223-229
8) Epstein JI, Fynheer J : Acidic mucin in the prostate : can it differentiate adenosis from adenocarcinoma? Hum Pathol 1992, 23 : 1321-1325
9) Baisden BL, Kahane H, Epstein JI : Perineural invasion, mucinous fibroplasia, and glomerulations : diagnostic features of limited cancer on prostate needle biopsy. Am J Surg Pathol 1999, 23 : 918-924
10) Bastacky SI, Walsh PC, Epstein JI : Relationship between perineural tumor invasion on needle biopsy and radical prostatectomy capsular penetration in clinical stage B adenocarcinoma of the prostate. Am J Surg Pathol 1993, 17 : 336-341
11) Epstein JI, Grignon DJ, Humphrey PA et al : Interobserver reproducibility in the diagnosis of prostatic intraepithelial neoplasia. Am J Surg Pathol 1995, 19 : 873-886
12) Cina SJ, Epstein JI : Adenocarcinoma of the prostate with atrophic features. Am J Surg Pathol 1997, 21 : 289-295
13) Humphrey PA, Kaleem Z, Swanson PE et al : Pseudohyperplastic prostatic adenocarcinoma. Am J Surg Pathol 1998, 22 : 1239-1246
14) Nelson RS, Epstein JI : Prostatic carcinoma with abundant xanthomatous cytoplasm. Foamy gland carcinoma. Am J Surg Pathol 1996, 20 : 419-426
15) Ro JY, Grignon DJ, Ayala AG et al : Mucinous adenocarcinoma of the prostate : histochemical and immunohistochemical studies. Hum Pathol 1990, 21 : 593-600
16) Ro JY, el-Naggar A, Ayala AG et al : Signetring-cell carcinoma or the prostate. Electron-microscopic and immunohistochemical studies of eight cases. Am J Surg Pathol 1988, 12 : 453-460
17) McNeal JE, Bostwick DG : Intraductal dysplasia : a premalignant lesion of the prostate. Hum Pathol 1986, 17 : 64-71
18) McNeal JE, Reese JH, Redwine EA et al : Cribriform adenocarcinoma of the prostate. Cancer 1986, 58 : 1714-1719
19) Guo CC, Epstein JI : Intraductal carcinoma of the prostate on needle biopsy : histologic features and clinical significance. Mod Pathol 2006, 19 : 1528-1535
20) Greene LF, Farrow GM, Ravits JM et al : Prostatic adenocarcinoma of ductal origin. J Urol 1979, 121 : 303-305
21) Tavora F, Epstein JI : High-grade prostatic intraepithelial neoplasia like ductal adenocarcinoma of the prostate : a clinicopathological study of 28 cases. Am J Surg Pathol 2008, 32 : 1060-1067
22) Adlakha H, Bostwick DG : Paneth cell-like change in prostatic adenocarcinoma represents neuroendocrine differentiation : report of 30 cases. Hum Pathol 1994, 25 : 135-139
23) Yao JL, Madeb R, Bourne P et al : Small cell carcinoma of the prostate : an immunohistochemical study. Am J Surg Pathol 2006, 30 : 705-712
24) Evans AJ, Humphrey PA, Belani J et al : Large cell neuroendocrine carcinoma of prostate : a clinicopathologic summary of 7 cased of a rare manifestation of advanced prostate cancer. Am J Surg Pathol 2006, 30 : 684-693
25) Giordano S, Tolonen T, Tolonen T et al : A pure primary low grade neuroendocrine carcinoma (carcinoid tumor) of the prostate. Int Urol Nephrol 2010, 42 : 683-687
26) Greene LF, O'Dea MJ, Dockerty MB : Primary transitional cell carcinoma of the prostate. J Urol 1976, 116 : 761-763
27) Schellhammer PF, Bean MA, Whitmore WF Jr : Prostatic involvement by transitional cell carcinoma : pathogenesis, patterns and prognosis. J Urol 1977, 118 : 399-403
28) Chibber PJ, MaIntyre MA, Hindmarsh JR et al : Transitional cell carcinoma involving the prostate. Br J Urol 1981, 53 : 605-609
29) Magi-Galluzzi C, Evans A, Delahunt B et al : International Society of Urological Pathology (ISUP) Consensus Conference on Handling and Staging of Radical Prostatectomy Specimens. Working group 3 : extraprostatic extension, lymphovascular invasion and locally advanced disease. Mod Pathol 2011, 24 : 26-38
30) Brossner C, Ringhofer H, Hernady T et al : Lymphatic drainage of prostatic transition and peripheral zones visualized on a three-dimensional workstation. Urology 2001, 57 : 389-393
31) Bubendorf L, Schopfer A, Wagner U et al : Metastatic patterns of prostate cancer : an autopsy study of 1, 589 patients. Hum Pathol 2000, 31 : 578-583
32) Gleason DF : Classification of prostatic carcinomas. Cancer Chemother Rep 1966, 50 : 125-128
33) Epstein JI, Egevad L, Amin MB et al : The 2014 International Society of Urological Pathology (ISUP) Consensus Conference on Gleason Grading of Prostatic Carcinoma. Am J Surg Pathol 2016, 40 : 244-252
34) Moch H, Humphrey PA, Ulbright TM et al : WHO classification of tumors of the urinary system and male genital organs. International Agency for Research on Cancer, 2016, 154
35) Smith DM, Murphy WM : Histologic changes in prostate carcinomas treated with leuprolide (luteinizing hormone-releasing hormone effect). Distinction from poor tumor differentiation. Cancer 1994, 73 : 1472-1477
36) Herawi M, Parwani AV, Irie J et al : Small glandular proliferations on needle biopsies : most common benign mimickers of prostatic adenocarcinoma sent in for expert second opinion. Am J Surg Pathol 2005, 29 : 874-880
37) Amin MB, Tamboli P, Varma M et al : Postatrophic hyperplasia of the prostate gland : a detailed analysis of its morphology in needle biopsy specimens. Am J Surg Pathol 1999, 23 : 925-931
38) Gaudin PB, Epstein JI : Adenosis of the prostate : morphologic criteria for its distinction from well-differentiated carcinoma. Hum Pathol 1993, 24 : 819-832
39) Devaraj LT, Bostwick DG : Atypical basal cell hyperplasia of the prostate. Immunophenotypic profile and proposed classification of basal cell proliferations. Am J Surg Pathol 1993, 17 : 645-659
40) Ali TZ, Epstein JI : Basal cell carcinoma of the prostate : a clinicopathologic study of 29 cases. Am J Surg Pathol 2007, 31 : 697-705
41) Grignon DJ, O'Malley FP : Mucinous metaplasia in the prostate gland. Am J Surg Pathol 1993, 17 : 287-290
42) Arias-Stella J, Takano-Morton J : Atypical epithelial changes in the seminal vesicle. AMA Arch Pathol 1958, 66 : 761-766
43) Gagucas RJ, Brown RW, Wheeler TM : Verumontanum mucosal gland hyperplasia. Am J Surg Pathol 1995, 19 : 30-36
44) Bostwick DG, Egbert BM, Fajardo LF : Radiation injury of the normal and neoplastic prostate. Am J Surg Pathol 1982, 6 : 541-551
45) Luque RJ, Lopez-Beltran A, Perez-Seoane C et al : Sclerosing adenosis of the prostate. Histologic features in needle biopsy specimens. Arch Pathol Lab Med 2003, 127 : e14-e16
46) Chuang AY, Epstein JI : Xanthoma of the prostate : a mimicker of high-grade prostate adenocarcinoma. Am J Surg Pathol 2007, 31 : 1225-1230
47) Ayala AG, Srigley JR, Ro JY et al : Clear cell cribriform hyperplasia of prostate. Report of 10 cases. Am J Surg Pathol 1986, 10 : 665-671
48) Bostwick DG, Amin MB, Dundore P et al : Architectural patterns of high-grade prostatic intraepithelial neoplasia. Hum Pathol 1993, 24 : 298-310
49) Ostrowski ML, Wheeler TM : Paraganglia of the prostate. Location, frequency, and differentiation from prostatic adenocarcinoma. Am J Surg Pathol 1994, 18 : 412-420
50) Oderda M, Mondaini N, Bartletti R et al : Leiomyoma of the genitourinary tract : a case series from the "rare urological neoplasm" registry. Scand J Urol 2013, 47 : 158-162
51) Vandoros GP, Manolidis T, Karamouzis MV et al : Leiomyosarcoma of the prostate : case report and review of 54 previously published cases. Sarcoma 2008 : 458709
52) Sexton WJ, Lance RE, Reyes AO et al : Adult prostate sarcoma : the M.D. Anderson cancer center experience. J Urol 2001, 166 : 521-525
53) Gaudin PB, Rosai J, Epstein JI : Sarcomas and related proliferative lesions of specialized prostatic stroma : a clinicopathologic study of 22 cases. Am J Surg Pathol 1998, 22 : 148-162
54) Herawi M, Epstein JI : Specialized stromal tumors of the prostate : a clinicopathologic study of 50 cases. Am J Surg Pathol 2006, 30 : 694-704
55) Osunkoya AO, Netto GJ, Epstein JI : Colorectal adenocarcinoma involving the prostate : report of 9 cases. Hum Pathol 2007, 38 : 1836-1841
56) Pitkanen P, Westermark P, Cornwell GG 3rd et al : Amyloid of the seminal vesicles. Adistinctive and common localized form of senile amyloidosis. Am J Pathol 1983, 110 : 64-69
57) Kuo T, Gomez LG : Monstrous epithelial cells in human epididymis and seminal vesicles. A pseudomalignant change. Am J Surg Pathol 1981, 5 : 483-490
58) Krishnan R, Heal MR : Study of the seminal vesicles in acute epididymitis. Br J Urol 1991, 67 : 632-637
59) Katafigiotis I, Sfoungaristos I, Duvdevani M et al : Primary adenocarcinoma of the seminal vesicles. A review of the literature. Arch Ital Urol Androl 2016, 88 : 47-51
60) Ohori M, Scardino PT, Lapin SL et al : The mechanisms and prognostic significance of seminal vesicle involvement by prostate cancer. Am J Surg Pathol 1993, 17 : 1252-1261
P.1108 掲載の参考文献
1) Evans TN, Poland ML, Boving RL : Vaginal malformations. Am J Obstet Gynecol 1981, 141 : 910-920
2) Kupfer SR, Quigley CA, French FS : Male pseudohermaphroditism. Semin Perinatol 1992, 16 : 319-331
3) New MI : Female pseudohermaphroditism. Semin Perinatol 1992, 16 : 299-318
4) Koenig C, Tavassoli FA : Nodular hyperplasia, adenoma, and adenomyoma of Bartholin's gland. Int J Gynecol Pathol 1998, 17 : 289-294
5) Lynch PJ : 2006 International Society for the Study of Vulvovaginal Disease classification of vulvar dermatoses : a synopsis. J Low Genit Tract Dis 2007, 11 : 1-2
6) Lynch PJ, Moyal-Barracco M, Bogliatto F et al : 2006 ISSVD classification of vulvar dermatoses : pathologic subsets and their clinical correlates. J Reprod Med 2007, 52 : 3-9
7) Guerrero A, Venkatesan A : Inflammatory vulvar dermatoses. Clin Obstet Gynecol 2015, 58 : 464-475
8) Janovski NA, Ames S : Lichen sclerosus et atrophicus of the vulva : a poorly understood disease entity. Obstet Gynecol 1963, 22 : 697-708
9) Lascano EF, Leopoldo, Montes F et al : Lichen sclerosus et atrophicus in childhood. Report of 6 Cases. Obstet Gynecol 1964, 24 : 872-877
10) Lee A, Bradford J, Fischer G : Long-term management of adult vulvar lichen sclerosus : a prospective cohort study of 507 women. JAMA Dermatol 2015, 151 : 1061-1067
11) Virgili A, Levratti A, Marzola A et al : Retrospective histopathologic reevaluation of 18 cases of plasma cell vulvitis. J Reprod Med 2005, 50 : 3-7
12) Wilkinson EJ, Teixeira MR : Epithelial tumours, Tumours of the vulva. In : Tavassoli FA, Stratton MR eds., Pathology and Genetics of Tumours of the Breast and Female Genital Organs, IARC Press, 2003, 316-325
13) Crum CP, Herrington CS, McCluggage WG et al Epithelial tumors. In : Kurman RJ, Carcangiu ML, Herrington CS, Young RH, eds., WHO Classification of Tumours of Female Reproductive Organs, IARC Press, 2014, 232-242
14) Bai H, Cviko A, Granter S et al : Immunophenotypic and viral (human papillomavirus) correlates of vulvar seborrheic keratosis. Hum Pathol 2003, 34 : 559-564
15) Aguilera-Barrantes I, Magro C, Nuovo GJ : Verruca vulgaris of the vulva in children and adults : a nonvenereal type of vulvar wart. Am J Surg Pathol 2007, 31 : 529-535
16) Sideri M, Jones RW, Wilkinson EJ et al : Squamous vulvar intraepithelial neoplasia : 2004 modified terminology, ISSVD Vulvar Oncology Subcommittee. J Reprod Med 2005, 50 : 807-810
17) Smith JS, Backes DM, Hoots BE et al : Human papillomavirus type-distribution in vulvar and vaginal cancers and their associated precursors. Obstet Gynecol 2009, 113 : 917-924
18) Goldblum JR, Hart WR : Vulvar Paget's disease : a clinicopathologic and immunohistochemical study of 19 cases. Am J Surg Pathol 1997, 21 : 1178-1187
19) Wilkinson EJ, Brown HM : Vulvar Paget disease of urothelial origin : a report of three cases and a proposed classification of vulvar Paget disease. Hum Pathol 2002, 33 : 549-54
20) Iwasa Y, Fletcher CD : Distinctive prepubertal vulval fibroma : a hitherto unrecognized mesenchymal tumor of prepubertal girls : analysis of 11 cases. Am J Surg Pathol 2004, 28 : 1601-1608
21) Steeper TA, Rosai J : Aggressive angiomyxoma of the female pelvis and perineum. Report of nine cases of a distinctive type of gynecologic soft-tissue neoplasm. Am J Surg Pathol 1983, 7 : 463-475
22) McCluggage WG, Connolly L, McBride HA : HMGA2 is a sensitive but not specific immunohistochemical marker of vulvovaginal aggressive angiomyxoma. Am J Surg Pathol 2010, 34 : 1037-1042
23) Fletcher CD, Tsang WY, Fisher C et al : Angiomyofibroblastoma of the vulva. A benign neoplasm distinct from aggressive angiomyxoma. Am J Surg Pathol 1992, 16 : 373-382
24) Nielsen GP, Young RH, Dickersin GR et al : Angiomyofibroblastoma of the vulva with sarcomatous transformation ("angiomyofibrosarcoma"). Am J Surg Pathol 1997, 21 : 1104-1108
25) Nucci MR, Granter SR, Fletcher CD : Cellular angiofibroma : a benign neoplasm distinct from angiomyofibroblastoma and spindle cell lipoma. Am J Surg Pathol 1997, 21 : 636-644
26) Iwasa Y, Fletcher CD : Cellular angiofibroma : clinicopathologic and immunohistochemical analysis of 51 cases. Am J Surg Pathol 2004, 28 : 1426-1435
27) Yoshida A, Yoshida H, Yoshida M et al : Myoepithelioma-like tumors of the vulvar region : a distinctive group of SMARCB1-deficient neoplasms. Am J Surg Pathol 2015, 39 : 1102-1113
28) Guillou L, Wadden C, Coindre JM et al : "Proximal-type" epithelioid sarcoma, a distinctive aggressive neoplasm showing rhabdoid features. Clinicopathologic, immunohistochemical, and ultrastructural study of a series. Am J Surg Pathol 1997, 21 : 130-146
29) Kim HJ, Kim MH, Kwon J et al : Proximal-type epithelioid sarcoma of the vulva with INI1 diagnostic utility. Ann Diagn Pathol 2012, 16 : 411-415
30) McCluggage WG, Ganesan R, Hirschowitz L et al : Ectopic prostatic tissue in the uterine cervix and vagina : report of a series with a detailed immunohistochemical analysis. Am J Surg Pathol 2006, 30 : 209-215
31) Herbst AL, Scully RE : Adenocarcinoma of the vagina in adolescence. A report of 7 cases including 6 clear-cell carcinomas (so-called mesonephromas) . Cancer 1970, 25 : 745-757
32) Herbst AL, Scully RE, Robboy SJ : The significance of adenosis and clear-cell adenocarcinoma of the genital tract in young females. J Reprod Med 1975, 15 : 5-11
33) Laskin WB, Fetsch JF, Tavassoli FA : Superficial cervicovaginal myofibroblastoma : fourteen cases of a distinctive mesenchymal tumor arising from the specialized subepithelial stroma of the lower female genital tract. Hum Pathol 2001, 32 : 715-725
34) Kazakov DV, Stewart CJ, Kacerovska D et al : Prostatic-type tissue in the lower female genital tract : a morphologic spectrum, including vaginal tubulosquamous polyp, adenomyomatous hyperplasia of paraurethral Skene glands (female prostate), and ectopic lesion in the vulva. Am J Surg Pathol 2010, 34 : 950-955
35) Sandberg EC : The incidence and distribution of occult vaginal adenosis. Am J Obstet Gynecol 1968, 101 : 322-334
36) Sherman AI, Goldrath M, Berlin A et al : Cervical-vaginal adenosis after in utero exposure to synthetic estrogens. Obstet Gynecol 1974, 44 : 531-545
37) Robboy SJ, Hill EC, Sandberg EC et al : Vaginal adenosis in women born prior to the diethylstilbestrol era. Human pathology 1986, 17 : 488-492
38) Robboy SJ, Young RH, Welch WR et al : Atypical vaginal adenosis and cervical ectropion. Association with clear cell adenocarcinoma in diethylstilbestrol-exposed offspring. Cancer 1984, 54 : 869-875
39) Bosch FX, Lorincz A, Munoz N et al : The causal relation between human papillomavirus and cervical cancer. J Clin Pathol 2002, 55 : 244-265
40) Mikami Y : Non-human-papillomavirus (HPV) -related adenocarcinomas and their precursors. In : Herrington CS ed., Pathology of the cervix, Springer, 2017, 185-199
41) Crosbie EJ, Einstein MH, Franceschi S et al : Human papillomavirus and cervical cancer. Lancet 2013, 382 : 889-899
42) Munoz N, Bosch FX, de Sanjose S et al : Epidemiologic classification of human papillomavirus types associated with cervical cancer. N Engl J Med 2003, 348 : 518-527
43) Cho NH, Kang S, Hong S et al : Multinucleation of koilocytes is in fact multilobation and is related to aberration of the G2 checkpoint. J Clin Pathol 2005, 58 : 576-582
44) McIntosh PB, Laskey P, Sullivan K et al : E1--E4-mediated keratin phosphorylation and ubiquitylation : a mechanism for keratin depletion in HPV16-infected epithelium. J Cell Sci 2010, 123 : 2810-2822
45) Richart RM, Barron BA : A follow-up study of patients with cervical dysplasia. Am J Obstet Gynecol 1969, 105 : 386-393
46) The 1988 Bethesda System for Reporting Cervical/Vaginal Cytologic Diagnoses. Developed and approved at a National Cancer Institute Workshop, Bethesda, Maryland, U.S.A., December 12-13, 1988. J Reprod Med 1989, 34 : 779-785
47) Stoler M, Bergeron C, Colgan TJ et al Squamous cell tumors and precursors. In : Kurman RJ, Carcangiu ML, Herrington CS, Young RH eds., WHO Classification of Tumours of Female Reproductive Organs, IARC Press, 2014
48) Darragh TM, Colgan TJ, Cox JT et al : The lower anogenital squamous terminology standardization project for HPV-associated lesions : background and consensus recommendations from the College of American Pathologists and the American Society for Colposcopy and Cervical Pathology. J Low Genit Tract Dis 2012, 16 : 205-242
49) 日本産婦人科学会, 日本病理学会 : 子宮頸癌取扱い規約 病理編, 第4版, 金原出版, 2017
50) Nagura M, Koshiyama M, Matsumura N et al : Clinical approaches to treating papillary squamous cell carcinoma of the uterine cervix. BMC Cancer 2014, 14 : 784
51) Grayson W, Cooper K : A reappraisal of "basaloid carcinoma" of the cervix, and the differential diagnosis of basaloid cervical neoplasms. Adv Anat Pathol 2002, 9 : 290-300
52) Masuda M, Abiko K, Minamiguchi S et al : Case of rapidly progressing condylomatous squamous cell carcinoma of the uterine cervix associated with low-risk human papillomavirus type 6. J Obstet Gynaecol Res 2018, 44 : 583-587
53) Frega A, Lukic A, Nobili F et al : Verrucous carcinoma of the cervix : detection of carcinogenetic human papillomavirus types and their role during follow-up. Anticancer Res 2007, 27 : 4491-4494
54) Wilbur DC, Colgan TJ, Ferenczy TJ et al : Glandular tumours and precursors. WHO Classification of Tumours of Female Reproductive Organs, 4th ed., IARC Press, 2014
55) Park JJ, Sun D, Quade BJ et al : Stratified mucin-producing intraepithelial lesions of the cervix : adenosquamous or columnar cell neoplasia? Am J Surg Pathol 2000, 24 : 1414-1419
56) Lastra RR, Park KJ, Schoolmeester JK : Invasive stratified mucin-producing carcinoma and stratified mucin-producing intraepithelial lesion (SMILE) : 15 cases presenting a spectrum of cervical neoplasia with description of a distinctive variant of invasive adenocarcinoma. Am J Surg Pathol 2016, 40 : 262-269
57) Stolnicu S, Barsan I, Hoang L et al : International endocervical adenocarcinoma criteria and classification (IECC) : A new pathogenetic classification for invasive adenocarcinomas of the endocervix. Am J Surg Pathol 2018, 42 : 214-226
58) Stolnicu S, Hoang L, Chiu D et al : Clinical outcomes of HPV-associated and unassociated endocervical adenocarcinomas categorized by the international endocervical adenocarcinoma criteria and classification (IECC). Am J Surg Pathol 2019, 43 : 466-474
59) Association of Directors of Anatomic and Surgical Pathology : Recommendations for the reporting of surgical specimens containing uterine cervical neoplasms. Am J Clin Pathol 2000, 114 : 847-851
60) Kojima A, Mikami Y, Sudo T et al : Gastric morphology and immunophenotype predict poor outcome in mucinous adenocarcinoma of the uterine cervix. Am J Surg Pathol 2007, 31 : 664-672
61) Park KJ, Kiyokawa T, Soslow RA et al : Unusual endocervical adenocarcinomas : an immunohistochemical analysis with molecular detection of human papillomavirus. Am J Surg Pathol 2011, 35 : 633-646
62) Carleton C, Hoang L, Sah S et al : A detailed immunohistochemical analysis of a large series of cervical and vaginal gastric-type adenocarcinomas. Am J Surg Pathol 2016, 40 : 636-644
63) Karamurzin YS, Kiyokawa T, Parkash V et al : Gastric-type endocervical adenocarcinoma : an aggressive tumor with unusual metastatic patterns and poor prognosis. Am J Surg Pathol 2015, 39 : 1449-1457
64) Kojima A, Shimada M, Mikami Y et al : Chemoresistance of gastric-type mucinous carcinoma of the uterine cervix : a study of the sankai gynecology study group. Int J Gynecol Cancer 2018, 28 : 99-106
65) Scully RE, Robboy SJ, Herbst AL : Vaginal and cervical abnormalities, including clear-cell adenocarcinoma, related to prenatal exposure to stilbestrol. Ann Clin Lab Sci 1974, 4 : 222-233
66) Kenny SL, McBride HA, Jamison J et al : Mesonephric adenocarcinomas of the uterine cervix and corpus : HPV-negative neoplasms that are commonly PAX8, CA125, and HMGA2 positive and that may be immunoreactive with TTF1 and hepatocyte nuclear factor 1-beta. Am J Surg Pathol 2012, 36 : 799-807
67) Stolnicu S, Barsan I, Hoang L et al : Diagnostic algorithmic proposal based on comprehensive immunohistochemical evaluation of 297 invasive endocervical adenocarcinomas. Am J Surg Pathol 2018, 42 : 989-1000
68) Mikami Y, McCluggage WG : Endocervical glandular lesions exhibiting gastric differentiation : an emerging spectrum of benign, premalignant, and malignant lesions. Adv Anat Pathol 2013, 20 : 227-237
69) Matsubara A, Sekine S, Ogawa R et al : Lobular endocervical glandular hyperplasia is a neoplastic entity with frequent activating GNAS mutations. Am J Surg Pathol 2014, 38 : 370-376
70) Colgan TJ, Hirschowitz L, Kim KR et al Other epithelial tumors. In : Kurman RJ, Carcangiu ML, Herrington CS, Young RH eds., WHO Classification of Tumours of Female Reproductive Organs, IARC Press, 2014, 194-196
71) Lennerz JK, Perry A, Mills JC et al : Mucoepidermoid carcinoma of the cervix : another tumor with the (t 11, 19) -associated CRTC1-MAML2 gene fusion. Am J Surg Pathol 2009, 33 : 835-843
72) Colgan TJ, Hirschowitz L, Kim KR et al : Neuroendocrine tumors. In : Kurman RJ, Carcangiu ML, Herrington CS, Young RH eds., WHO Classification of Tumours of Female Reproductive Organs, IARC Press, 2014, 196-198
73) Mannion C, Park WS, Man YG et al : Endocrine tumors of the cervix : morphologic assessment, expression of human papillomavirus, and evaluation for loss of heterozygosity on 1p, 3p, 11q, and 17p. Cancer 1998, 83 : 1391-1400
74) Gadducci A, Carinelli S, Aletti G : Neuroendrocrine tumors of the uterine cervix : A therapeutic challenge for gynecologic oncologists. Gynecol Oncol 2017, 144 : 637-646
75) Kuji S, Watanabe R, Sato Y et al : A new marker, insulinoma-associated protein 1 (INSM1), for high-grade neuroendocrine carcinoma of the uterine cervix : Analysis of 37 cases. Gynecol Oncol 2017, 144 : 384-390
76) Hariri J, Ingemanssen JL : Multinucleated stromal giant cells of the uterine cervix. Int J Gynecol Pathol 1993, 12 : 228-234
77) Nucci MR, Young RH, Fletcher CD : Cellular pseudosarcomatous fibroepithelial stromal polyps of the lower female genital tract : an underrecognized lesion often misdiagnosed as sarcoma. Am J Surg Pathol 2000, 24 : 231-240
78) Siddon A, Hui P : Glial heterotopia of the uterine cervix : DNA genotyping confirmation of its fetal origin. Int J Gynecol Pathol 2010, 29 : 394-397
79) Gilks CB, Young RH, Clement PB et al : Adenomyomas of the uterine cervix of of endocervical type : a report of ten cases of a benign cervical tumor that may be confused with adenoma malignum [corrected]. Mod Pathol 1996, 9 : 220-224
80) Grayson W, Taylor LF, Cooper K : Carcinosarcoma of the uterine cervix : a report of eight cases with immunohistochemical analysis and evaluation of human papillomavirus status. Am J Surg Pathol 2001, 25 : 338-347
81) Copeland LJ, Sneige N, Ordonez NG et al : Endodermal sinus tumor of the vagina and cervix. Cancer 1985, 55 : 2558-2565
P.1139 掲載の参考文献
1) McCluggage WG : Benign Diseases of the Endometrium. Blaustein's Pathology of the Female Genital Tract, 6th ed, In : Kurman RJ, Ellenson LH, Ronnett BM, editors., Springer, 2011, 305-358
2) Wheeler DT, Bristow RE, Kurman RJ : Histologic alterations in endometrial hyperplasia and well-differentiated carcinoma treated with progestins. Am J Surg Pathol 2007, 31 : 988-998
3) Park HJ, Kim YS, Yoon TK et al : Chronic endometritis and infertility. Clin Exp Reprod Med 2016, 43 : 185-192
4) Cohen I : Endometrial pathologies associated with postmenopausal tamoxifen treatment. Gynecol Oncol 2004, 94 : 256-266
5) Hileeto D, Fadare O, Martel M et al : Age dependent association of endometrial polyps with increased risk of cancer involvement. World J Surg Oncol 2005, 3 : 8
6) Eken MK, Kaygusuz EI, G II et al : Endometrial malignancies arising on endometrial polyps and precursor lesions. Eur J Gynaecol Oncol 2016, 37 : 827-832
7) Fletcher JA, Pinkus JL, Lage JM et al : Clonal 6p21 rearrangement is restricted to the mesenchymal component of an endometrial polyp. Genes Chromosomes Cancer 1992, 5 : 260-263
8) Hendrickson MR, Kempson RL : Endometrial epithelial metaplasias : proliferations frequently misdiagnosed as adenocarcinoma. Report of 89 cases and proposed classification. Am J Surg Pathol 1980, 4 : 525-542
9) Rawish KR, Desouki MM, Fadare O : Atypical mucinous glandular proliferations in endometrial samplings : follow-up and other clinicopathological findings in 41 cases. Hum Pathol 2017, 63 : 53-62
10) Kurman RJ, Kaminski PF, Norris HJ : The behavior of endometrial hyperplasia. A long-term study of "untreated" hyperplasia in 170 patients. Cancer 1985, 56 : 403-412
11) Mutter GL : Endometrial intraepithelial neoplasia (EIN) : will it bring order to chaos? The Endometrial Collaborative Group. Gynecol Oncol 2000, 76 : 287-290
12) Kurman RJ, Norris HJ : Evaluation of criteria for distinguishing atypical endometrial hyperplasia from well-differentiated carcinoma. Cancer 1982, 49 : 2547-2559
13) Setiawan VW, Yang HP, Pike MC et al : Type I and II endometrial cancers : have they different risk factors? J Clin Oncol 2013, 31 : 2607-2618
14) Bokhman JV : Two pathogenetic types of endometrial carcinoma. Gynecol Oncol 1983, 15 : 10-17
15) Matias-Guiu X, Prat J : Molecular pathology of endometrial carcinoma. Histopathology 2013, 62 : 111-123
17) Howitt BE, Shukla SA, Sholl LM et al : Association of polymerase e-mutated and microsatellite-instable endometrial cancers with neoantigen load, number of tumor-infiltrating lymphocytes, and expression of PD-1 and PD-L1. JAMA Oncol 2015, 1 : 1319-1323
18) Santin AD, Bellone S, Buza N et al : Regression of chemotherapy-resistant polymerase epsilon (POLE) ultra-mutated and MSH6 hyper-mutated endometrial tumors with Nivolumab. Clin Cancer Res 2016, 22 : 5682-5687
19) Kihara A, Yoshida H, Watanabe R et al : Clinicopathologic association and prognostic value of microcystic, elongated, and fragmented (MELF) pattern in endometrial endometrioid carcinoma. Am J Surg Pathol 2017, 41 : 896-905
20) Kounelis S, Kapranos N, Kouri E et al : Immunohistochemical profile of endometrial adenocarcinoma : a study of 61 cases and review of the literature. Mod Pathol 2000, 13 : 379-388
21) Saegusa M, Okayasu I : Frequent nuclear beta-catenin accumulation and associated mutations in endometrioid-type endometrial and ovarian carcinomas with squamous differentiation. J Pathol 2001, 194 : 59-67
22) Djordjevic B, Hennessy BT, Li J et al : Clinical assessment of PTEN loss in endometrial carcinoma : immunohistochemistry outperforms gene sequencing. Mod Pathol 2012, 25 : 699-708
23) Tashiro H, Isacson C, Levine R et al : p53 gene mutations are common in uterine serous carcinoma and occur early in their pathogenesis. Am J Pathol 1997, 150 : 177-185
24) Yemelyanova A, Ji H, Shih IeM et al : Utility of p16 expression for distinction of uterine serous carcinomas from endometrial endometrioid and endocervical adenocarcinomas : immunohistochemical analysis of 201 cases. Am J Surg Pathol 2009, 33 : 1504-1514
25) Ju B, Wang J, Yang B et al : Morphologic and immunohistochemical study of clear cell carcinoma of the uterine endometrium and cervix in comparison to ovarian clear cell carcinoma. Int J Gynecol Pathol 2018, 37 : 388-396
26) Pocrnich CE, Ramalingam P, Euscher ED et al : Neuroendocrine carcinoma of the endometrium : a clinicopathologic study of 25 cases. Am J Surg Pathol 2016, 40 : 577-586
27) Altrabulsi B, Malpica A, Deavers MT et al : Undifferentiated carcinoma of the endometrium. Am J Surg Pathol 2005, 29 : 1316-1321
28) Tafe LJ, Garg K, Chew I et al : Endometrial and ovarian carcinomas with undifferentiated components : clinically aggressive and frequently underrecognized neoplasms. Mod Pathol 2010, 23 : 781-789
29) Hoang L, Chiang S, Lee CH : Endometrial stromal sarcomas and related neoplasms : new developments and diagnostic considerations. Pathology 2018, 50 : 162-177
30) Chu PG, Arber DA, Weiss LM et al : Utility of CD10 in distinguishing between endometrial stromal sarcoma and uterine smooth muscle tumors : an immunohistochemical comparison of 34 cases. Mod Pathol 2001, 14 : 465-471
31) Lee CH, Marino-Enriquez A, Ou W et al : The clinicopathologic features of YWHAE-FAM22 endometrial stromal sarcomas : a histologically high-grade and clinically aggressive tumor. Am J Surg Pathol 2012, 36 : 641-653
32) Lee CH, Ali RH, Rouzbahman M et al : Cyclin D1 as a diagnostic immunomarker for endometrial stromal sarcoma with YWHAE-FAM22 rearrangement. Am J Surg Pathol 2012, 36 : 1562-1570
33) Chiang S, Lee CH, Stewart CJR et al : BCOR is a robust diagnostic immunohistochemical marker of genetically diverse high-grade endometrial stromal sarcoma, including tumors exhibiting variant morphology. Mod Pathol 2017, 30 : 1251-1261
34) Lewis N, Soslow RA, Delair DF et al : ZC3H7BBCOR high-grade endometrial stromal sarcomas : a report of 17 cases of a newly defined entity. Mod Pathol 2018, 31 : 674-684
35) Marino-Enriquez A, Lauria A, Przybyl J et al : BCOR internal tandem duplication in high-grade uterine sarcomas. Am J Surg Pathol 2018, 42 : 335-341
36) de Leval L, Lim GS, Waltregny D et al : Diverse phenotypic profile of uterine tumors resembling ovarian sex cord tumors : an immunohistochemical study of 12 cases. Am J Surg Pathol 2010, 34 : 1749-1761
37) Croce S, de Kock L, Boshari T et al : Uterine Tumor Resembling Ovarian Sex Cord Tumor (UTROSCT) commonly exhibits positivity with sex cord markers FOXL2 and SF-1 but lacks FOXL2 and DICER1 mutations. Int J Gynecol Pathol 2016, 35 : 301-308
38) Moore M, McCluggage WG : Uterine tumour resembling ovarian sex cord tumour : first report of a large series with follow-up. Histopathology 2017, 71 : 751-759
39) Oliva E, Young RH, Amin MB et al : An immunohistochemical analysis of endometrial stromal and smooth muscle tumors of the uterus : a study of 54 cases emphasizing the importance of using a panel because of overlap in immunoreactivity for individual antibodies. Am J Surg Pathol 2002, 26 : 403-412
40) Sun X, Mittal K : MIB-1 (Ki-67), estrogen receptor, progesterone receptor, and p53 expression in atypical cells in uterine symplastic leiomyomas. Int J Gynecol Pathol 2010, 29 : 51-54
41) Mills AM, Ly A, Balzer BL et al : Cell cycle regulatory markers in uterine atypical leiomyoma and leiomyosarcoma : immunohistochemical study of 68 cases with clinical follow-up. Am J Surg Pathol 2013, 37 : 634-642
42) Bennett JA, Lamb C, Young RH : Apoplectic leiomyomas : a morphologic analysis of 100 cases highlighting unusual features. Am J Surg Pathol 2016, 40 : 563-568
43) Prayson RA, Goldblum JR, Hart WR : Epithelioid smooth-muscle tumors of the uterus : a clinicopathologic study of 18 patients. Am J Surg Pathol 1997, 21 : 383-391
44) Carr RJ, Hui P, Buza N : Intravenous leiomyomatosis revisited : an experience of 14 cases at a single medical center. Int J Gynecol Pathol 2015, 34 : 169-176
45) Barnas E, Ksiazek M, Ras R et al : Benign metastasizing leiomyoma : a review of current literature in respect to the time and type of previous gynecological surgery. PLoS One 2017, 12 : e0175875
46) Patton KT, Cheng L, Papavero V et al : Benign metastasizing leiomyoma : clonality, telomere length and clinicopathologic analysis. Mod Pathol 2006, 19 : 130-140
47) Bell SW, Kempson RL, Hendrickson MR : Problematic uterine smooth muscle neoplasms. A clinicopathologic study of 213 cases. Am J Surg Pathol 1994, 18 : 535-558
48) Gupta M, Laury AL, Nucci MR et al : Predictors of adverse outcome in uterine smooth muscle tumours of uncertain malignant potential (STUMP) : a clinicopathological analysis of 22 cases with a proposal for the inclusion of additional histological parameters. Histopathology 2018, 73 : 284-298
49) Ip PP, Cheung AN, Clement PB : Uterine smooth muscle tumors of uncertain malignant potential (STUMP) : a clinicopathologic analysis of 16 cases. Am J Surg Pathol 2009, 33 : 992-1005
50) Nakayama H, Teramoto H, Teramoto M : True incidence of uterine adenomatoid tumors. Biomed Rep 2013, 1 : 352-354
51) Tamura D, Maeda D, Halimi SA et al : Adenomatoid tumour of the uterus is frequently associated with iatrogenic immunosuppression. Histopathology 2018, 73 : 1013-1022
52) Musella A, De Felice F, Kyriacou AK et al : Perivascular epithelioid cell neoplasm (PEComa) of the uterus : A systematic review. Int J Surg 2015, 19 : 1-5
53) Bennett JA, Braga AC, Pinto A et al : Uterine PEComas : a morphologic, immunohistochemical, and molecular analysis of 32 tumors. Am J Surg Pathol 2018, 42 : 1370-1383
54) Haimes JD, Stewart CJR, Kudlow BA et al : Uterine inflammatory myofibroblastic tumors frequently harbor ALK fusions with IGFBP5 and THBS1. Am J Surg Pathol 2017, 41 : 773-780
55) Mohammad N, Haimes JD, Mishkin S et al : ALK is a specific diagnostic marker for inflammatory myofibroblastic tumor of the uterus. Am J Surg Pathol 2018, 42 : 1353-1359
56) Chiang S, Cotzia P, Hyman DM et al : NTRK fusions define a novel uterine sarcoma subtype with features of fibrosarcoma. Am J Surg Pathol 2018, 42 : 791-798
57) Kolin DL, Dong F, Baltay M et al : SMARCA4-deficient undifferentiated uterine sarcoma (malignant rhabdoid tumor of the uterus) : a clinicopathologic entity distinct from undifferentiated carcinoma. Mod Pathol 2018, 31 : 1442-1456
59) Gilks CB, Clement PB, Hart WR et al : Uterine adenomyomas excluding atypical polypoid adenomyomas and adenomyomas of endocervical type : a clinicopathologic study of 30 cases of an underemphasized lesion that may cause diagnostic problems with brief consideration of adenomyomas of other female genital tract sites. Int J Gynecol Pathol 2000, 19 : 195-205
60) Horita A, Kurata A, Maeda D et al : Immunohistochemical characteristics of atypical polypoid adenomyoma with special reference to h-caldesmon. Int J Gynecol Pathol 2011, 30 : 64-70
61) Heatley MK : Atypical polypoid adenomyoma : a systematic review of the English literature. Histopathology 2006, 48 : 609-610
62) Liu Y, Weber Z, San Lucas FA et al : Assessing inter-component heterogeneity of biphasic uterine carcinosarcomas. Gynecol Oncol 2018, 151 : 243-249
63) Silverberg SG, Major FJ, Blessing JA et al : Carcinosarcoma (malignant mixed mesodermal tumor) of the uterus. A Gynecologic Oncology Group pathologic study of 203 cases. Int J Gynecol Pathol 1990, 9 : 1-19
64) Ferguson SE, Tornos C, Hummer A et al : Prognostic features of surgical stage I uterine carcinosarcoma. Am J Surg Pathol 2007, 31 : 1653-1661
P.1186 掲載の参考文献
1) Medeiros F, Muto MG, Lee Y et al : The tubal fimbria is a preferred site for early adenocarcinoma in women with familial ovarian cancer syndrome. Am J Surg Pathol 2006, 30 : 230-236
2) Fernandez-Acenero MJ, Cordova S : Cutaneous endometriosis : review of 15 cases diagnosed at a single institution. Arch Gynecol Obstet 2011, 283 : 1041-1044
3) McCluggage WG, O'Rourke D, McElhenney C et al : Mullerian papilloma-like proliferation arising in cystic pelvic endosalpingiosis. Hum Pathol 2002, 33 : 944-946
4) Kurman RJ, Carcangiu ML, Herrington CS et al eds : WHO Classification of tumours of female reproductive organs, 4th ed, IARC Press, 2014
5) 日本産婦人科学会, 日本病理学会編 : 卵巣腫瘍・卵管癌・腹膜癌取扱い規約, 病理編, 第1版, 金原出版, 2016
6) 日本産科婦人科学会 : 婦人科腫瘍委員会報告, 2017年度患者年報. 日本産婦人科学会誌 2019, 71 : 669-724
7) Brierley JD, Gospodarowicz MK, Wittekind C (eds) : Ovarian, Fallopian Tube, and Primary Peritoneal Carcinoma, 2017
8) 日本産科婦人科学会 : 婦人科腫瘍委員会報告, 第60回治療報告. 日本産婦人科学会誌 2019, 71 : 725-802
9) 国立がん研究センターがん対策情報センター : がん情報サービス, がんの統計. https://ganjoho.jp/reg_stat/statistics/dl/index.html
10) 北正人 : 婦人科がん (第2版) -最新の研究動向-, 卵巣がん, 卵巣癌の発生, 卵巣癌の疫学. 日本臨床 2018, 76 : 491-498
11) Nakonechny QB, Gilks CB : Ovarian Cancer in Hereditary Cancer Susceptibility Syndromes. Surg Pathol Clin 2016, 9 : 189-199
12) 小林浩 : 卵巣腫瘍卵巣子宮内膜症と卵巣癌, 長期間の疫学調査よりみた卵巣子宮内膜症の癌化について. 病理と臨床 2006, 24 : 243-248
13) Baker PM, Oliva E : Immunohistochemistry as a tool in the differential diagnosis of ovarian tumors : an update. Int J Gynecol Pathol 2005, 24 : 39-55.
14) Kobel M, Kalloger SE, Carrick J et al : A limited panel of immunomarkers can reliably distinguish between clear cell and high-grade serous carcinoma of the ovary. Am J Surg Pathol 2009, 33 : 14-21
15) Ordonez NG : Value of PAX 8 immunostaining in tumor diagnosis : a review and update. Adv Anat Pathol 2012, 19 : 140-151
16) Iwamoto M, Nakatani Y, Fugo K et al : Napsin A is frequently expressed in clear cell carcinoma of the ovary and endometrium. Hum Pathol 2015, 46 : 957-962
17) Lim D, Ip PP, Cheung AN et al : Immunohistochemical comparison of ovarian and uterine endometrioid carcinoma, endometrioid carcinoma with clear cell change, and clear cell carcinoma. Am J Surg Pathol 2015, 39 : 1061-1069
18) Kurman RJ, Shih IeM : Molecular pathogenesis and extraovarian origin of epithelial ovarian cancer--shifting the paradigm. Hum Pathol 2011, 42 : 918-931
20) Lee Y, Miron A, Drapkin R et al : A candidate precursor to serous carcinoma that originates in the distal fallopian tube. J Pathol 2007, 211 : 26-35
21) Seidman JD, Kurman RJ : Ovarian serous borderline tumors : a critical review of the literature with emphasis on prognostic indicators. Hum Pathol 2000, 31 : 539-557
22) Deavers MT, Gershenson DM, Tortolero-Luna G et al : Micropapillary and cribriform patterns in ovarian serous tumors of low malignant potential : a study of 99 advanced stage cases. Am J Surg Pathol 2002, 26 : 1129-1141
23) Hauptmann S, Friedrich K, Redline R et al : Ovarian borderline tumors in the 2014 WHO classification : evolving concepts and diagnostic criteria. Virchows Arch 2017, 470 : 125-142
24) Zeppernick F, Ardighieri L, Hannibal CG et al : BRAF mutation is associated with a specific cell type with features suggestive of senescence in ovarian serous borderline (atypical proliferative) tumors. Am J Surg Pathol 2014, 38 : 1603-1611
25) Fader AN, Java J, Ueda S et al : Survival in women with grade 1 serous ovarian carcinoma. Obstet Gynecol 2013, 122 : 225-232
26) Malpica A, Deavers MT, Lu K et al : Grading ovarian serous carcinoma using a two-tier system. Am J Surg Pathol 2004, 28 : 496-504
27) Soslow RA, Han G, Park KJ et al : Morphologic patterns associated with BRCA1 and BRCA2 genotype in ovarian carcinoma. Mod Pathol 2012, 25 : 625-636
28) Ali RH, Seidman JD, Luk M et al : Transitional cell carcinoma of the ovary is related to highgrade serous carcinoma and is distinct from malignant brenner tumor. Int J Gynecol Pathol 2012, 31 : 499-506
29) Takeuchi T, Ohishi Y, Imamura H et al : Ovarian transitional cell carcinoma represents a poorly differentiated form of high-grade serous or endometrioid adenocarcinoma. Am J Surg Pathol 2013, 37 : 1091-1099
30) Kindelberger DW, Lee Y, Miron A et al : Intraepithelial carcinoma of the fimbria and pelvic serous carcinoma : Evidence for a causal relationship. Am J Surg Pathol 2007, 31 : 161-169
31) Casey L, Singh N : Ovarian high-grade serous carcinoma : assessing pathology for site of origin, staging and post-neoadjuvant chemotherapy changes. Surg Pathol Clin 2019, 12 : 515-528
32) Singh N, Gilks CB, Hirschowitz L et al : Primary site assignment in tubo-ovarian high-grade serous carcinoma : Consensus statement on unifying practice worldwide. Gynecol Oncol 2016, 141 : 195-198
33) Singh N, Gilks CB, Hirshowitz L et al : Adopting a uniform approach to site assignment in tubo-ovarian high-grade serous carcinoma : the time has come. Int J Gynecol Pathol 2016, 35 : 230-237
34) McCluggage WG, Judge MJ, Clarke BA et al : Data set for reporting of ovary, fallopian tube and primary peritoneal carcinoma : recommendations from the International Collaboration on Cancer Reporting (ICCR). Mod Pathol 2015, 28 : 1101-1122
35) Hart WR : Mucinous tumors of the ovary : a review. Int J Gynecol Pathol 2005, 24 : 4-25
36) Romeo M, Pons F, Barretina P et al : Incomplete staging surgery as a major predictor of relapse of borderline ovarian tumor. World J Surg Oncol 2013, 11 : 13
37) du Bois A, Ewald-Riegler N, de Gregorio N et al : Borderline tumours of the ovary : A cohort study of the Arbeitsgmeinschaft Gynakologische Onkologie (AGO) Study Group. Eur J Cancer 2013, 49 : 1905-1914
38) Ludwick C, Gilks CB, Miller D et al : Aggressive behavior of stage I ovarian mucinous tumors lacking extensive infiltrative invasion : a report of four cases and review of the literature. Int J Gynecol Pathol 2005, 24 : 205-217
40) Tabrizi AD, Kalloger SE, Kobel M et al : Primary ovarian mucinous carcinoma of intestinal type : significance of pattern of invasion and immunohistochemical expression profile in a series of 31 cases. Int J Gynecol Pathol 2010, 29 : 99-107
41) Zaino RJ, Brady MF, Lele SM et al : Advanced stage mucinous adenocarcinoma of the ovary is both rare and highly lethal : a Gynecologic Oncology Group study. Cancer 2011, 117 : 554-562
42) Prat J, Young RH, Scully RE : Ovarian mucinous tumors with foci of anaplastic carcinoma. Cancer 1982, 50 : 300-304
43) Provenza C, Young RH, Prat J : Anaplastic carcinoma in mucinous ovarian tumors : a clinicopathologic study of 34 cases emphasizing the crucial impact of stage on prognosis, their histologic spectrum, and overlap with sarcomalike mural nodules. Am J Surg Pathol 2008, 32 : 383-389
44) Kuo KT, Mao TL, Jones S et al : Frequent activating mutations of PIK3CA in ovarian clear cell carcinoma. Am J Pathol 2009, 174 : 1597-1601
45) Jones S, Wang TL, Shih IeM et al : Frequent mutations of chromatin remodeling gene ARID1A in ovarian clear cell carcinoma. Science 2010, 330 : 228-231
46) Wiegand KC, Shah SP, Al-Agha OM et al : ARID1A mutations in endometriosis-associated ovarian carcinomas. N Engl J Med 2010, 363 : 1532-1543
47) 前田大, 木藤正 : 癌の分子病理学病理診断から治療標的探索まで, (第2部) 癌の分子病理学, 臓器癌, 卵巣癌. 病理と臨床 2016, 34 : 205-220
48) Chui MH, Ryan P, Radigan J et al : The histomorphology of Lynch syndrome-associated ovarian carcinomas : toward a subtype-specific screening strategy. Am J Surg Pathol 2014, 38 : 1173-1181
49) Lewis MR, Deavers MT, Silva EG et al : Ovarian involvement by metastatic colorectal adenocarcinoma : still a diagnostic challenge. Am J Surg Pathol 2006, 30 : 177-184
50) 清川貴子, 浜田智美 : 病理診断に役立つ免疫組織化学の新しいマーカー, 卵巣顆粒膜細胞腫と類内膜腺癌の鑑別への応用. 診断病理 2007, 24 : 18-20
51) Young RH : Ovarian sex cord-stromal tumours and their mimics. Pathology 2018, 50 : 5-15
52) Young RH : From Krukenberg to today : the ever present problems posed by metastatic tumors in the ovary. Part II. Adv Anat Pathol 2007, 14 : 149-177
53) Prat J : Ovarian carcinomas, including secondary tumors : diagnostically challenging areas. Mod Pathol 2005, 18 Suppl 2 : S99-111
54) Laury AR, Perets R, Piao H et al : A comprehensive analysis of PAX8 expression in human epithelial tumors. Am J Surg Pathol 2011, 35 : 816-826
55) Rabban JT, Lerwill MF, McCluggage WG et al : Primary ovarian carcinoid tumors may express CDX-2 : a potential pitfall in distinction from metastatic intestinal carcinoid tumors involving the ovary. Int J Gynecol Pathol 2009, 28 : 41-48
56) Rabban JT, Zaloudek CJ : A practical approach to immunohistochemical diagnosis of ovarian germ cell tumours and sex cord-stromal tumours. Histopathology 2013, 62 : 71-88
57) Kuhn E, Ayhan A, Shih IeM et al : The pathogenesis of atypical proliferative Brenner tumor : an immunohistochemical and molecular genetic analysis. Mod Pathol 2014, 27 : 231-237
58) Liao XY, Xue WC, Shen DH et al : p63 expression in ovarian tumours : a marker for Brenner tumours but not transitional cell carcinomas. Histopathology 2007, 51 : 477-483
59) Logani S, Oliva E, Amin MB et al : Immunoprofile of ovarian tumors with putative transitional cell (urothelial) differentiation using novel urothelial markers : histogenetic and diagnostic implications. Am J Surg Pathol 2003, 27 : 1434-1441
60) Hamada T, Kiyokawa T, Nomura K et al : Immunohistochemical analysis of reserve cell-like cells of ovarian mullerian mucinous/mixed epithelial borderline tumor. Int J Gynecol Pathol 2008, 27 : 199-206
61) Lim D, Oliva E : Ovarian sex cord-stromal tumours : an update in recent molecular advances. Pathology 2018, 50 : 178-189
62) 前田大地 : 卵巣腫瘍 II-病理診断の実際-, Microcystic stromal tumor, 新たな卵巣腫瘍の疾患概念. 病理と臨床 2015, 33 : 1085-1093
64) Roth LM, Czernobilsky B : Perspectives on pure ovarian stromal neoplasms and tumor-like proliferations of the ovarian stroma. Am J Surg Pathol 2011, 35 : e15-33
65) Stall JN, Young RH : Granulosa cell tumors of the ovary with prominent thecoma-like foci : a report of 16 cases emphasizing the ongoing utility of the reticulin stain in the modern era. Int J Gynecol Pathol 2019, 38 : 143-150
66) Young RH, Dickersin GR, Scully RE : Juvenile granulosa cell tumor of the ovary. A clinicopathological analysis of 125 cases. Am J Surg Pathol 1984, 8 : 575-596
67) Wang X, Ma Z, Li Y : Ovarian yolk sac tumor : the experience of a regional cancer center. Int J Gynecol Cancer 2016, 26 : 884-891
68) Shojaei H, Hong H, Redline RW : High-level expression of divergent endodermal lineage markers in gonadal and extra-gonadal yolk sac tumors. Mod Pathol 2016, 29 : 1278-1288
69) Nogales FF, Dulcey I, Preda O : Germ cell tumors of the ovary : an update. Arch Pathol Lab Med 2014, 138 : 351-362
70) Witkowski L, Goudie C, Foulkes WD et al : Small-cell carcinoma of the ovary of hypercalcemic type (malignant rhabdoid tumor of the ovary) : a review with recent developments on pathogenesis. Surg Pathol Clin 2016, 9 : 215-226
71) Young RH, Oliva E, Scully RE : Small cell carcinoma of the ovary, hypercalcemic type. A clinicopathological analysis of 150 cases. Am J Surg Pathol 1994 18 : 1102-1116
72) Jelinic P, Schlappe BA, Conlon N et al : Concomitant loss of SMARCA2 and SMARCA4 expression in small cell carcinoma of the ovary, hypercalcemic type. Mod Pathol 2016, 29 : 60-66
73) Young RH : From krukenberg to today : the ever present problems posed by metastatic tumors in the ovary : part I. Historical perspective, general principles, mucinous tumors including the krukenberg tumor. Adv Anat Pathol 2006, 13 : 205-227.
74) Lee KR, Young RH : The distinction between primary and metastatic mucinous carcinomas of the ovary : gross and histologic findings in 50 cases. Am J Surg Pathol 2003, 27 : 281-292
75) Khunamornpong S, Suprasert P, Pojchamarnwiputh S et al : Primary and metastatic mucinous adenocarcinomas of the ovary : Evaluation of the diagnostic approach using tumor size and laterality. Gynecol Oncol 2006, 101 : 152-157
76) Elishaev E, Gilks CB, Miller D et al : Synchronous and metachronous endocervical and ovarian neoplasms : evidence supporting interpretation of the ovarian neoplasms as metastatic endocervical adenocarcinomas simulating primary ovarian surface epithelial neoplasms. Am J Surg Pathol 2005, 29 : 281-294
77) Ronnett BM, Kajdacsy-Balla A, Gilks CB et al : Mucinous borderline ovarian tumors : points of general agreement and persistent controversies regarding nomenclature, diagnostic criteria, and behavior. Hum Pathol 2004, 35 : 949-960.
78) Riopel MA, Ronnett BM, Kurman RJ : Evaluation of diagnostic criteria and behavior of ovarian intestinal-type mucinous tumors : atypical proliferative (borderline) tumors and intraepithelial, microinvasive, invasive, and metastatic carcinomas. Am J Surg Pathol 1999, 23 : 617-635
79) Vang R, Gown AM, Zhao C et al : Ovarian mucinous tumors associated with mature cystic teratomas : morphologic and immunohistochemical analysis identifies a subset of potential teratomatous origin that shares features of lower gastrointestinal tract mucinous tumors more commonly encountered as secondary tumors in the ovary. Am J Surg Pathol 2007, 31 : 854-869
80) Heatley MK : Immunohistochemical biomarkers of value in distinguishing primary ovarian carcinoma from gastric carcinoma : a systematic review with statistical meta-analysis. Histopathology 2008, 52 : 267-276
81) Lee KR, Scully RE : Mucinous tumors of the ovary : a clinicopathologic study of 196 borderline tumors (of intestinal type) and carcinomas, including an evaluation of 11 cases with 'pseudomyxoma peritonei'. Am J Surg Pathol 2000, 24 : 1447-1464.
82) Kiyokawa T, Young RH, Scully RE : Krukenberg tumors of the ovary : a clinicopathologic analysis of 120 cases with emphasis on their variable pathologic manifestations. Am J Surg Pathol 2006, 30 : 277-299
83) Bennett JA, Young RH, Chuang AY et al : Ovarian metastases of breast cancers with signet ring cells : a report of 17 cases including 14 Krukenberg tumors. Int J Gynecol Pathol 2018, 37 : 507-515
84) Alvarado-Cabrero I, Stolnicu S, Kiyokawa T et al : Carcinoma of the fallopian tube : Results of a multi-institutional retrospective analysis of 127 patients with evaluation of staging and prognostic factors. Ann Diagn Pathol 2013, 17 : 159-164
85) Young RH : Neoplasms of the fallopian tube and broad ligament : a selective survey including historical perspective and emphasising recent developments. Pathology 2007, 39 : 112-124
86) Heatley MK : Is female adnexal tumour of probable wolffian origin a benign lesion? A systematic review of the English literature. Pathology 2009, 41 : 645-648
87) Tiltman AJ, Allard U : Female adnexal tumours of probable Wolffian origin : an immunohistochemical study comparing tumours, mesonephric remnants and paramesonephric derivatives. Histopathology 2001, 38 : 237-242
88) Goyal A, Masand RP, Roma AA : Value of PAX-8 and SF-1 immunohistochemistry in the distinction between female adnexal tumor of probable wolffian origin and its mimics. Int J Gynecol Pathol 2016, 35 : 167-175
P.1215 掲載の参考文献
1) Lewis SH, Post MD, Benirschke K : Placenta. Histology for Pathologist, 4th ed., Lippincott Williams & Wilkins, 2012, 1149-1181
2) 南口早智子 : 胎盤, 病理診断に直結した組織学. 病理と臨床 2017, 35 (臨時増刊号) : 349-361
3) 佐藤勇一郎 : 胎盤の肉眼所見の取り方と検体の扱い方. 病理と臨床 2014, 32 : 494-502
4) Klaus FT, Redline RW, Gersell DJ et al : Placental Pathology, Atlas of Nontumor Pathology, The American Registry of Pathology, 2004, 312
5) Hargitai B, Marton T, Cox PM : Best practice no 178. Examination of the human placenta. J Clin Pathol 2004, 57 : 785-792
6) Langston C, Kaplan C, Macpherson T et al : Practice guideline for examination of the placenta : developed by the Placental Pathology Practice Guideline Development Task Force of the College of American Pathologists. Arch Pathol Lab Med 1997, 121 : 449-476
7) 松岡健太郎 : 双胎胎盤の病理. 病理と臨床 2014, 32 : 518-523
8) 中山雅弘 : 目でみる胎盤病理, 医学書院, 2002, 19-22
9) Baergen RN : Manual of Pathology of the Human Placenta, 2nd ed., Springer, 2011, 3-426
11) Nowak C, Joubert M, Jossic F et al : Perinatal prognosis of pregnancies complicated by placental chronic villitis or intervillositis of unknown etiology and combined lesions : about a series of 178 cases. Placenta 2016, 44 : 104-108
12) Tsuge M, Hida AI, Minematsu T et al : Prospective cohort study of congenital cytomegalovirus infection during pregnancy with fetal growth restriction : serologic analysis and placental pathology. J Pediatr 2019, 206 : 42-48
13) 金井瑞恵, 錦信吾, 有馬雄三ほか : 先天梅毒児の臨床像および母親の背景情報に関する研究報告 (2016-2017年). IASR 2018, 39 : 205-206
14) Qureshi F, Jacques SM, Reyes MP : Placental histopathology in syphilis. Hum Pathol 1993, 23 : 779-784
15) 渡辺員支 : 妊娠高血圧症候群の新たな定義・臨床分類. 臨床婦人科産科 2018, 72 : 634-639
16) Karumanchi SA, Maynard SE, Stillman IE : Preeclampsia : a renal perspective. Kidney Int 2005, 67 : 2101-2113
17) Stanek J : Placental pathology varies in hypertensive conditions of pregnancy. Virchow Arch 2018, 472 : 415-423
18) Veerbeek JH, Nikkeks PG, Torrance HL et al : Placental pathology in early intrauterine growth restriction associated with maternal hypertension. Placenta 2014, 35 : 696-701
20) ACOG Committee on Obstetric Practice : ACOG committee opinion. Number 266, January 2002 : placenta accreta. Obstet Gynecol 2002, 99 : 169-170
21) Sugiyama S, Itakura A, Ota T et al : Placenta previa increta/percreta in Japan-a retrospective study of ultrasound findings, management and clinical course. J Obstet Gynecol Res 2007, 33 : 606-611
23) Kurman RJ, Carcangiu ML, Herrington CS et al : WHO Classification of Tumours of Female Reproductive Organs, 4th ed., IARC, 2014, 158-167
24) 日本産科婦人科学会・日本病理学会編 : 絨毛性疾患取扱い規約, 第3版, 金原出版, 2011
25) Matsui H, Iitsuka Y, Yamazawa K et al : Changes in the incidence of molar pregnancies. A population-based study in Chiba Prefecture and Japan between 1974 and 2000. Hum Reprod 2003, 18 : 172-175
26) Eysbouts YK, Bulten J, Ottevenger PB et al : Trends in incidence for gestational trophoblastic disease over the last 20 years in a population-based study. Gynecol Oncol 2016, 140 : 70-75
27) Berkowitz RS, Goldstein DP : Clinical practice. Molar pregnancy. N Engl J Med 2009, 360 : 1639-1645
28) Ronnet BM : Hydatidiform moles : ancilliary techniques to refine diagnosis. Arch Pathol Lab Med 2018, 142 : 1485-1502
29) Pham T, Steele J, Stayboldt C et al : Placental mesenchymal dysplasia is associated with high rates of intrauterine growth restriction and fetal demise : A report of 11 new cases and a review of the literature. Am J Clin Pathol 2006, 126 : 67-78
32) Yver M, Carles D, Bloch B et al : Determination of DNA ploidy by fluorescence in situ hybridization (FISH) in hydatidiform moles : evaluation of FISH on isolated nuclei. Hum Pathol 2004, 35 : 752-758
33) Gaber LW, Redline RW, Mostoufi-Zadeh M et al : Invasive partial mole. Am J Clin Pathol 1986, 85 : 722-724
34) Hui P : Gestational trophoblastic tumors : a timely review of diagnostic pathology. Arch Pathol Lab Med 2019, 143 : 65-74
35) Liu J, Guo L : Intraplacental choriocarcinoma in a term placenta with both maternal and infantile metastases : a case report and review of the literature. Gynecol Oncol 2006, 103 : 1147-1151
36) Stichelbout M, Devisme L, Franquet-Ansart H et al : SALL4 expression in gestational trophoblastic tumors : a useful tool to distinguish choriocarcinoma from placental site trophoblastic tumor and epithelioid trophoblastic tumor. Hum Pathol 2016, 54 : 121-126
37) Shih IM, Kurman RJ : p63 expression is useful in the distinction of epithelioid trophoblastic and placental site trophoblastic tumors by profiling trophoblastic subpopulations. Am J Surg Pathol 2004, 28 : 1177-1183
38) Schmid P, Nagai Y, Agarwal R et al : Prognostic markers and long-term outcome of placental-site trophoblastic tumours : a retrospective observational study. Lancet 2009, 374 : 48-55
40) Fadare O, Parkash V, Carcangiu ML et al : Epithelioid trophoblastic tumor : clinicopathological features with an emphasis on uterine cervical involvement. Mod Pathol 2006, 19 : 75-82
41) Amer HZ, Heller DS : Chorangioma and related vascular lesions of the placenta--a review. Fetal Pediatr Pathol 2010, 29 : 199-206
42) Yee EU, Hale G, Liu X et al : Hepatocellular adenoma of the placenta with updated immunohistochemical and molecular markers : a case report. Int J Surg Pathol 2016, 24 : 640-643
43) Valenzano Menada M, Moioli M, Garaventa A et al : Spontaneous regression of transplacental metastases from maternal melanoma in a newborn : case report and review of the literature. Melanoma Res 2010, 20 : 443-449
44) Lynn AA, Parry SI, Morgan MA et al : Disseminated congenital neuroblastoma involving the placenta. Arch Pathol Lab Med 1997, 121 : 741-744
45) Ravishankar S, Hoffman L, Lertsburapa T et al : Extensive placental choriovascular infiltration by maturing myeloid cells in down syndrome-associated transient abnormal myelopoiesis. Pediatr Dev Pathol 2015, 18 : 231-236
P.1260 掲載の参考文献
1) 森谷卓也 : 正常乳房の基本的な組織像. 乳腺腫学, 第2版, 日本乳癌学会編, 金原出版, 2016, 2-7
2) Boecker W, Buerger H : Evidence of progenitor cells of glandular and myoepithelial cell lineages in the human adult female breast epithelium : a new progenitor (adult stem) cell concept. Cell Prolif 2003, 36 Suppl 1 : 73-84
3) 日本乳癌学会編 : 乳癌取扱い規約, 第18版, 金原出版, 2018
4) WHO Classification of Tumours of Editorial Board ed : WHO Classification of Tumours, 5 th ed, Breast Tumours, IARC Press, 2019
5) Usami S, Moriya T, Kasajima A et al : Pathological aspects of core needle biopsy for non-palpable breast lesions. Breast Cancer 2005, 12 : 272-278
6) Perou CM, Sorlie T, Eisen MB et al : Molecular portraits of human breast tumours. Nature 2000, 406 : 747-752
7) Carey LA, Perou CM, Livasy CA et al : Race, breast cancer subtypes, and survival in the Carolina Breast Cancer Study. JAMA 2006, 295 : 2492-2502
8) Rastelli F, Biancanelli S, Falzetta A et al : Triple-negative breast cancer : current state of the art. Tumori 2010, 96 : 875-888
9) Curigliano G, Burstein HJ, Winer EP et al : De-escalating and escalating treatments for early-stage breast cancer. the St. Gallen International Expert Consensus Conference on the Primary Therapy of Early Breast Cancer 2017. Ann Oncol 2017, 28 : 1700-1712
10) Mayer IA, Abramson VG, Lehmann BD et al : New strategies for triple-negative breast cancer--deciphering the heterogeneity. Clin Cancer Res 2014, 20 : 782-790
11) 日本乳癌学会編 : 乳癌診療ガイドライン 2 疫学・診断編 2018年版, 第4版, 金原出版, 2018
12) Patani N, Mokbel K : Clinical significance of sentinel lymph node isolated tumour cells in breast cancer. Breast Cancer Res Treat 2011, 127 : 325-334
13) Brennick JB, Yan S : False-positive cells in sentinel lymph nodes. Semin Diagn Pathol 2008, 25 : 116-119
14) Nihon-Yanagi Y, Ueda T, Kameda N et al : A case of ectopic breast cancer with a literature review. Surg Oncol 2011, 20 : 35-42
15) Barreto DS, Sedgwick EL, Nagi CS et al : Granulomatous mastitis : etiology, imaging, pathology, treatment, and clinical findings. Breast Cancer Res Treat 2018, 171 : 527-534
16) Hwang MJ, Brown H, Murrin R et al : Breast implant-associated anaplastic large cell lymphoma : a case report and literature review. Aesthetic Plast Surg 2015, 39 : 391-395
17) Fellegara G, Kuhn E : Perineural and intraneural "invasion" in benign proliferative breast disease. Int J Surg Pathol 2007, 15 : 286-287
18) Wen YH, Weigelt B, Reis-Filho JS : Microglandular adenosis : a non-obligate precursor of triple-negative breast cancer? Histol Histopathol 2013, 28 : 1099-1108
19) Ha SM, Cha JH, Shin HJ et al : Radial scars/com-plex sclerosing lesions of the breast : radiologic and clinicopathologic correlation. BMC Med Imaging 2018, 18 : 39
20) Lakhani SR, Ellis IO, Schnitt SJ et al ed : WHO Classification of Tumours of the Breast, 4th ed, IARC Press, 2012
21) Bombonati A, Sgroi DC : The molecular pathology of breast cancer progression. J Pathol 2011, 223 : 307-317
22) 森谷卓也, 鹿股直樹, 小塚祐司 : 非浸潤性乳管癌および乳管内病変の病理診断 最近の話題も含めて. 診断病理 2011, 28 : 79-89
23) Moriya T, Kozuka Y, Kanomata N et al : The role of immunohistochemistry in the differential diagnosis of breast lesions. Pathology 2009, 41 : 68-76
24) Gomes DS, Porto SS, Balabram D et al : Inter-observer variability between general pathologists and a specialist in breast pathology in the diagnosis of lobular neoplasia, columnar cell lesions, atypical ductal hyperplasia and ductal carcinoma in situ of the breast. Diagn Pathol 2014, 9 : 121
25) Said SM, Visscher DW, Nassar A et al : Flat epithelial atypia and risk of breast cancer : A Mayo cohort study. Cancer 2015, 121 : 1548-1555
26) Moriya T : Development of breast carcinoma in relationships to the intrinsic subtype. In Pathology of female breast cancers : Precursor and early-stage breast, ovarian and uterine carcinomas, Springer, 2018, 73-79
27) Ni YB, Tse GM : Pathological criteria and practical issues in papillary lesions of the breast-a review. Histopathology 2016, 68 : 22-32
28) Matsubayashi RN, Momosaki S, Muranaka T : Ductal adenoma of breast : imaging characteristics and radiologic-pathologic correlation of unique findings which reflect "pseudoinvasion". Breast Cancer 2016, 23 : 597-606
29) Yoon JY, Chitale D : Adenomyoepithelioma of the breast. A brief diagnostic review. Arch Pathol Lab Med 2013, 137 : 725-729
30) Moritz AW, Wiedenhoefer JF, Profit AP et al : Breast adenomyoepithelioma and adenomyoepithelioma with carcinoma (malignant adenomyoepithelioma) with associated breast malignancies : A case series emphasizing histologic, radiologic, and clinical correlation. Breast 2016, 29 : 132-139
31) Atkins KA, Cohen MA, Nicholson B et al : Atypical lobular hyperplasia and lobular carcinoma in situ at core breast biopsy. Use of careful radiologic-pathologic correlation to recommend excision or observation. Radiology 2013, 269 : 340-347
32) Sen LQ, Berg WA, Hooley RJ et al : Core breast biopsies showing lobular carcinoma in situ should be excised and surveillance is reasonable for atypical lobular hyperplasia. AJR Am J Roentgenol 2016, 207 : 1132-1145
33) Ginter PS, D'Alfonso TM : Current concepts in diagnosis, molecular features, and management of lobular carcinoma in situ of the breast with a discussion of morphologic variants. Arch Pathol Lab Med 2017, 141 : 1668-1678
34) Tan PH, Schnitt SJ, van de Vijver MJ et al : Papillary and neuroendocrine breast lesions : the WHO stance. Histopathology 2015, 66 : 761-770
35) Kuo SH, Lo C, Chen YH et al : Prognostic significance of clinicopathologic features in patients with breast ductal carcinoma-in-situ who received breast-conserving surgery. Clin Breast Cancer 2018, 18 : 441-450
36) Moritani S, Ichihara S, Hasegawa M et al : Topographical, morphological and immunohistochemical characteristics of carcinoma in situ of the breast involving sclerosing adenosis. Two distinct topographical patterns and histological types of carcinoma in situ. Histopathology 2011, 58 : 835-846
37) Yang M, Moriya T, Oguma M et al : Microinvasive ductal carcinoma (T1mic) of the breast. The clinicopathological profile and immunohistochemical features of 28 cases. Pathol Int 2003, 53 : 422-428
38) Ohashi R, Hayama A, Matsubara M et al : Breast carcinoma with osteoclast-like giant cells : A cytological-pathological correlation with a literature review. Ann Diagn Pathol 2018, 33 : 1-5
39) Tsuda H, Akiyama F, Kurosumi M et al : Evaluation of the interobserver agreement in the number of mitotic figures of breast carcinoma as simulation of quality monitoring in the Japan National Surgical Adjuvant Study of Breast Cancer (NSAS-BC) protocol. Jpn J Cancer Res 2000, 91 : 451-457
40) Rakha EA, El-Sayed ME, Lee AH et al : Prognostic significance of Nottingham histologic grade in invasive breast carcinoma. J Clin Oncol 2008, 26 : 3153-3158
41) Green AR, Soria D, Powe DG et al : Nottingham prognostic index plus (NPI+) predicts risk of distant metastases in primary breast cancer. Breast Cancer Res Treat 2016, 157 : 65-75
42) Cuzick J, Dowsett M, Pineda S et al : Prognostic value of a combined estrogen receptor, progesterone receptor, Ki-67, and human epidermal growth factor receptor 2 immunohistochemical score and comparison with the Genomic Health recurrence score in early breast cancer. J Clin Oncol 2011, 29 : 4273-4278
43) Allred DC, Harvey JM, Berardo M et al : Prognostic and predictive factors in breast cancer by immunohistochemical analysis. Mod Pathol 1998, 11 : 155-168
44) Wolff AC, Hammond MEH, Allison KH et al : Human Epidermal Growth Factor Receptor 2 Testing in breast cancer. American Society of Clinical Oncology/College of American Pathologists clinical practice guideline focused update. J Clin Oncol 2018, 36 : 2105-2122
45) Leung SCY, Nielsen TO, Zabaglo LA et al : Analytical validation of a standardised scoring protocol for Ki67 immunohistochemistry on breast cancer excision whole sections : an international multicentre collaboration. Histopathology 2019, 75 : 225-235
46) Hida AI, Bando K, Sugita A et al : Visual assessment of Ki67 using a 5-grade scale (Eye-5) is easy and practical to classify breast cancer subtypes with high reproducibility. J Clin Pathol 2015, 68 : 356-361
47) Al-Baimani K, Bazzarelli A, Clemons M et al : Invasive pleomorphic lobular carcinoma of the breast. Pathologic, clinical, and therapeutic considerations. Clin Breast Cancer 2015, 15 : 421-425
48) Gunhan-Bilgen I, Oktay A : Tubulolobular carcinoma of the breast : clinical, mammographic and sonographic findings. Eur J Radiol 2006, 60 : 418-424
49) Canas-Marques R, Schnitt SJ : E-cadherin immunohistochemistry in breast pathology. Uses and pitfalls. Histopathology 2016, 68 : 57-69
50) Dabbs DJ, Bhargava R, Chivukula M : Lobular versus ductal breast neoplasms : the diagnostic utility of p120 catenin. Am J Surg Pathol 2007, 31 : 427-437
51) Moriya T, Kasajima A, Ishida K et al : New trends of immunohistochemistry for making differential diagnosis of breast lesions. Med Mol Morphol 2006, 39 : 8-13
52) Brandt SM, Young GQ, Hoda SA : The "Rosen Triad" : tubular carcinoma, lobular carcinoma in situ, and columnar cell lesions. Adv Anat Pathol 2008, 15 : 140-146
53) Cong Y, Qiao G, Zou H et al : Invasive cribriform carcinoma of the breast : A report of nine cases and a review of the literature. Oncol Lett 2015, 9 : 1753-1758
54) de Andrade Natal R, Derchain SF, Pavanello M et al : Expression of unusual immunohistochemical markers in mucinous breast carcinoma. Acta Histochem 2017, 119 : 327-336
55) Karabagli P, Kilic H : Primary pure signet cell carcinoma of the breast : a case report and review of the literature. Breast Cancer 2013, 20 : 363-366
56) Jaffer S, Bleiweiss IJ, Nagi CS : Benign mucocele-like lesions of the breast : revisited. Mod Pathol 2011, 24 : 683-687
57) Gibreel WO, Boughey JC : Mucocele-like lesions of the breast : rate of upstaging and cancer development. Ann Surg Oncol 2016, 23 : 3838-3842
58) Mateo AM, Pezzi TA, Sundermeyer M et al : Atypical medullary carcinoma of the breast has similar prognostic factors and survival to typical medullary breast carcinoma : 3, 976 cases from the National Cancer Data Base. J Surg Oncol 2016, 114 : 533-536
59) Suzuki T, Miki Y, Takagi K et al : Androgens in human breast carcinoma. Med Mol Morphol 2010, 43 : 75-81
60) Takahashi K, Wakasa T, Shintaku M : A case of rare primary cystic-type squamous cell carcinoma of the breast that could be preoperatively diagnosed. Asian J Surg 2017, 40 : 243-247
61) Carter MR, Hornick JL, Lester S et al : Spindle cell (sarcomatoid) carcinoma of the breast : a clinicopathologic and immunohistochemical analysis of 29 cases. Am J Surg Pathol 2006, 30 : 300-309
62) Dwyer JB, Clark BZ : Low-grade fibromatosis-like spindle cell carcinoma of the breast. Arch Pathol Lab Med 2015, 139 : 552-557
63) Downs-Kelly E, Nayeemuddin KM, Albarracin C et al : Matrix-producing carcinoma of the breast : an aggressive subtype of metaplastic carcinoma. Am J Surg Pathol 2009, 33 : 534-541
64) De la Cruz C, Moriya T, Endoh M et al : Invasive micropapillary carcinoma of the breast : clinicopathological and immunohistochemical study. Pathol Int 2004, 54 : 90-96
65) Moritani S, Ichihara S, Hasegawa M et al : Serous papillary adenocarcinoma of the female genital organs and invasive micropapillary carcinoma of the breast. Are WT1, CA125, and GCDFP-15 useful in differential diagnosis? Hum Pathol 2008, 39 : 666-671
66) Harrison BT, Fowler E, Krings G et al : Pan-TRK immunohistochemistry : a useful diagnostic adjunct for secretory carcinoma of the breast. Am J Surg Pathol 2019, 43 : 1693-1700
67) Treitl D, Radkani P, Rizer M : Adenoid cystic carcinoma of the breast, 20 years of experience in a single center with review of literature. Breast Cancer 2018, 25 : 228-233
68) Resetkova E, Albarracin C, Sneige N : Collagenous spherulosis of breast : morphologic study of 59 cases and review of the literature. Am J Surg Pathol 2006, 30 : 20-27
69) Otsuki Y, Yamada M, Shimizu S et al : Solid-papillary carcinoma of the breast : clinicopathological study of 20 cases. Pathol Int 2007, 57 : 421-429
70) Nayak A, Bleiweiss IJ, Dumoff K et al : Mucinous cystadenocarcinoma of the breast : Report of 2 cases including one with long-term local recurrence. Int J Surg Pathol 2018, 26 : 749-757
71) Foschini MP, Asioli S, Foreid S et al : Solid Papillary breast carcinomas resembling the tall cell variant of papillary thyroid neoplasms : A unique invasive tumor with indolent behavior. Am J Surg Pathol 2017, 41 : 887-895
72) Park S, Suh YL : Useful immunohistochemical markers for distinguishing Paget cells from Toker cells. Pathology 2009, 41 : 640-644
73) Krings G, Bean GR, Chen YY : Fibroepithelial lesions ; The WHO spectrum. Semin Diagn Pathol 2017, 34 : 438-452
74) Wu YT, Chen ST, Chen CJ et al : Breast cancer arising within fibroadenoma : collective analysis of case reports in the literature and hints on treatment policy. World J Surg Oncol 2014, 12 : 335
75) Lozada JR, Burke KA, Maguire A et al : Myxoid fibroadenomas differ from conventional fibroadenomas : a hypothesis-generating study. Histopathology 2017, 71 : 626-634
76) Zhang Y, Kleer CG : Phyllodes tumor of the breast : Histopathologic features, differential diagnosis, and molecular/genetic updates. Arch Pathol Lab Med 2016, 140 : 665-671
77) Tan BY, Acs G, Apple SK et al : Phyllodes tumours of the breast : a consensus review. Histopathology 2016, 68 : 5-21
78) Rakha EA, Aleskandarany MA, Lee AH et al : An approach to the diagnosis of spindle cell lesions of the breast. Histopathology 2016, 68 : 33-44
79) Drinka EK, Bargaje A, Ersahin CH et al : Pseudoangiomatous stromal hyperplasia (PASH) of the breast : a clinicopathological study of 79 cases. Int J Surg Pathol 2012, 20 : 54-58
80) Bonito FJP, de Almeida Cerejeira D, Dahlstedt-Ferreira C et al : Radiation-induced angiosarcoma of the breast : A review. Breast J 2019 [Epub ahead of print]
81) Fong D, Lann MA, Finlayson C et al : Diabetic (lymphocytic) mastopathy with exuberant lymphohistiocytic and granulomatous response : a case report with review of the literature. Am J Surg Pathol 2006, 30 : 1330-1336
82) Chau A, Jafarian N, Rosa M : Male breast : clinical and imaging evaluations of benign and malignant entities with histologic correlation. Am J Med 2016, 129 : 776-791
83) Ruddy KJ, Winer E : Male breast cancer : risk factors, biology, diagnosis, treatment, and survivorship. Ann Oncol 2013, 24 : 1434-1443
84) Asch-Kendrick R, Cimino-Mathews A : The role of GATA3 in breast carcinomas : a review. Hum Pathol 2016, 48 : 37-47
85) El Hag MI, Hag AM, Ha JP et al : Comparison of GATA-3, mammaglobin, GCDFP-15 expression in breast carcinoma in serous effusions : A cell-block micro-array study. Pleura Peritoneum 2017, 2 : 143-148
P.1296 掲載の参考文献
1) 大島孝一, 森坪麻友子 : リンパ節ならびに節外臓器の取り扱いかた. リンパ腫アトラス, 第5版, 文光堂, 2018, 41-44
2) 中村直哉 : 免疫組織化学とin situ hybridization. リンパ腫アトラス, 第5版, 文光堂, 2018, 20-25
3) 磯部泰司, 三浦偉久男 : 染色体・遺伝子検査. 日本臨牀 2014, 72 : 418-429
4) 大島孝一 : 悪性リンパ腫 : 検査方法, 診断, 分類, コンパニオン診断まで. SRL 宝函 2017, 37 : 11-21
5) Swerdlow SH, Campo E, Harris NL et al : WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. International Agency for Research on Cancer (IARC) Press, 2017
6) 横山雅大 : 悪性リンパ腫の抗体療法. 血液フロンティア 2010, 20 : 21-29
7) Cheson BD : Ofatumumab, a novel anti-CD20 monoclonal antibody for the treatment of B-cell malignancies. J Clin Oncol 2010, 28 : 3525-3530
8) 吉野正, 佐藤康晴 : リンパ組織の形態と機能. リンパ腫アトラス, 第5版, 文光堂, 2018, 12-19
9) Nosanchuk JS, Schnitzer B : Follicular hyperplasia in lymph nodes from patients with rheumatoid arthritis. A clinicopathologic study. Cancer 1969, 24 : 343-354
10) Kojima M, Hosomura Y, Itoh H et al : Reactive proliferative lesions in lymph nodes from rheumatoid arthritis patients. A clinicopathological and immunohistological study. Acta Pathol Jpn 1990, 40 : 249-254,
11) 高木敬三, 遠藤泰彦 : 木村病, リンパ節病変. 病理と臨床 1994, 12 (臨時増刊号) : 383-384
12) 石川栄世, 田中寿子ほか : 好酸球性リンパ濾胞様構造増生肉芽腫 (木村氏病) の病理学的研究. 日網内系会誌 1981, 20 (補) : 137-148
13) Ramchandani PL, Sabesan T, Hussein K : Angiolymphoid hyperplasia with eosinophilia masquerading as Kimura disease. Br J Oral Maxillofac Surg 2005, 43 : 249-252
14) 吉田泰徳 : 木村病. リンパ腫アトラス, 第5版, 文光堂, 2018, 356-359
15) Keller AR, Hochholzer L, Castleman B : Hyaline-vascular and plasma-cell types of giant lymph node hyperplasia of mediastinum and other locations. Cancer 1972, 29 : 670-683
16) Frizzera G : Atypical lymphoproliferative disorders. Neoplastic Hematopathology, 2nd ed, Knowles DM ed, Lippincott Williams&Wilkins, 2000, 569-622
17) Leger-Ravet MB, Pauchmaur M, Devergne O et al : Interleukin-6 gene expression in Castleman's disease. Blood 1991, 78 : 2923-2930
18) Ohbayashi JH, Ohbayashi K, Kawakubo K et al : Molecular genetic, cytogenetic and immunophenotypic analyses in Castleman's disease of the plasma cell type. Am J Clin Pathol 1994, 101 : 290-295
19) 中村博敏, 中世古知昭, 石井昭宏ほか : 血清IL-6が高値を示し染色体異常を認めた全身性Castleman病. 臨床血液 1993, 34 : 212-217
20) 佐久間秀夫, 森尚義, 小島瑞 : 多発性神経炎と内分泌症状を伴うplasma cell dyscrasia (病理的側面). 病理と臨床 1983, 1 : 1669-1682
21) Dispenzieri A, Kyle RA, Lacy MQ et al : POEMS syndrome : Definitions and long-term outcome. Blood 2003, 101 : 2496-2506
22) Takatsuki K, Sanada I : Plasma cell dyscrasia with polyneuropathy and endocrine disorder : Clinical and laboratory features of 109 reported cases. Jpn J Clin Oncol 1983, 13 : 543-555
23) 森茂郎, 毛利昇, 内田俊和 : 著しい多クローン性高γグロブリン血症と全身リンパ節の高度の形質細胞増殖を呈する症候群 : 形質細胞型Castlemanリンパ腫との異同. 日網内系会誌 1980, 20 (補) : 85-94
24) Kojima M, Nakamura S, Shimizu K et al : Clinical implication of idiopathic plasmacytic lymphadenopathy with polyclonal hypergammaglobulinemia. A report of 16 cases. Int J Surg Pathol 2004, 12 : 25-30
25) Kojima M, Nakamura S, Motoori T et al : Primary marginal zone B-cell lymphoma of the lymph node resembling plasmacytoma arising from a plasma cell variant of Castleman's disease. A clinicopathological and immunohistochemical study of seven patients. APMIS 110 : 875-880, 2002
26) 竹内真衣 : IgG4関連疾患. 病理と臨床 2017, 35 : 534-539
27) Sato Y, Yoshino T : IgG4-related lymphadenopathy. Int J Rheumatol 2012, 2012 : 572539
28) Umehara H, Okazaki K, Msaki Y et al : Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011. Mod Rheumatol 2012, 22 : 21-30
29) Ioachim HL, Medeiros, LJ : Ioachim's Lymph Node Pathology, 4th edition, Lippincott Williams & Wilkins, 2009
30) Oyama T, Ichimura K, Suzuki R et al : Senile EBV+ B-cell lymphoproliferative disorders : A clinicopathologic study of 22 patients. Am J Surg Pathol 2003, 27 : 16-26
31) 日本小児感染症学会監修 : 慢性活動性EBウイルス感染症とその類縁疾患の診療ガイドライン 2016, 診断と治療社, 2016
32) Ohshima K, Kikuchi M, Masuda Y et al : HTLV-I associated lymphadenitis. Cancer 1992, 69 : 239-248
33) Ohshima K, Suzumiya J, Kato A et al : Clonal HTLV-I-infected CD4+ lymphocytes and nonclonal non-HTLV-I-infected giant cells in incipient ATLL with Hodgkin-like histologic features. Int J Cancer 1997, 72 : 592-598
34) Pantaleo G, Graziosi C, Fauci AS : The immunopathogenesis of human immunodeficiency virus infection. N Engl J Med 1993, 328 : 327-335
35) Burns BF, Wood GS, Dorfman RF : The varied histopathology of lymphadenopathy in the homosexual male. Am J Surg Pathol 1985, 9 : 287-297
36) Katzin WE, Julius CJ, Tubbs RR et al : Lymphoproliferative disorders associated with carbamazepine. Arch Pathol Lab Med 1990, 114 : 1244-8
37) 菊池昌弘 : 特異な組織像を呈するリンパ節炎について. 日血会誌 1972, 35 : 379-380
38) Kikuchi M, Takeshita M, Eimoto T et al : Histiocytic necrotizing lymphadenitis : Clinicopathologic, immunologic and HLA typing study. Lymphoid Malignancy, Immunology and Cytogenetics, Hanaoka M, Kadin ME, Mikata A et al eds, Field & Wood, 1990, 251-257
39) Ohshima K, Kikuchi M, Sumiyoshi Y et al : Proliferating cells in histiocytic necrotizing lymphadenitis. Virchows Arch B Cell Pathol Incl Mol Pathol 1991, 61 : 97-100
40) Eimoto T, Kikuchi M, Mitsui T : Histiocytic necrotizing lymphadenitis. An ultrastructural study in comparison with other types of lymphadenitis. Acta Pathol Jpn 1983, 33 : 863-879
41) Hollingsworth HC, Peiper SC, Weiss LM et al : An investigation of the viral pathogenesis of Kikuchi-Fujimoto's disease. Lack of evidence for Epstein-Barr virus or human herpes type 6 as the causative agent. Arch Pathol Lab Med 1994, 118 : 134-140
42) Sheibani K, Fritz RM, Winberg CD et al : "Monocytoid" cells in reactive follicular hyperplasia with and without multifocal histiocytic reactions. An immunohistochemical study of 21 cases including suspected cases of toxoplasmic lymphadenitis. Am J Clin Pathol 1984, 81 : 435-458
43) Aozasa K, Ohsawa M, Horiuchi K et al : The occurrence of monocytoid B-lymphocytes in autoimmune disorders. Mod Pathol 1993, 6 : 121-124
44) Kojima M, Nakamura S, Itoh H et al : Occurrence of monocytoid B-cells in reactive lymph node lesions. Pathol Res Pract 1998, 194 : 559-565
45) Rosai J, Dorfman RF : Sinus histiocytosis with massive lymphadenopathy : A pseudolymphomatous benign disorder. Analysis of 34 cases. Cancer 1972, 30 : 1174-1188
46) Robb-Smith AHT, Taylor, CR : Lymph Node Biopsy : A Diagnostic Atlas, Miller Heyden, 1981, 132
47) Foucar E, Rosai J, Dorfman R : Sinus histiocytosis with massive lymphadenopathy (Rosai and Dorfman disease) : Review of the entity. Semin Diagn Pathol 1990, 7 : 19-73
48) Mepham BL : Fluorescence microscopy in histopathology. Selected Topics in Histopathology, Cook HC ed, Bailliere Tindall, 1973, 269-276
49) Ustredt HT : Usual and unusual reactions to B.C.G. inoculation in children. Am Rev Tuberc 1956, 74 : 32-42
50) al-Bhlal LA : Pathologic findings for bacille Calmette-Guerin infections in immunocompetent and immunocompromised patients. Am J Clin Pathol 2000, 113 : 703-708
51) 武村民子編 : 特集 サルコイドーシス ; 病変成立の理解のために. 病理と臨床 1995, 13 : 762-826
52) Scott MA, McCurley TL, Vnencak-Jones CL et al : Cat-scratch disease. Detection of Bartonella henselae DNA in archival biopsies from patients with clinically, serologically and histologically defined disease. Am J Pathol 1996, 149 : 2161-2167
53) Naji AF, Carbonell F, Baker HJ : Cat scratch disease. A report of three new cases, review of the literature, and classification of the pathologic changes in the lymph nodes during various stage of disease. Am J Clin Pathol 1962, 38 : 513-521
54) Kojima M, Nakamura S, Hosomura Y et al : Abscess- forming granulomatous lymphadenitis : Histological typing of suppurative granulomas and clinicopathological findings with special reference to cat scratch disease. Acta Pathol Jpn 1993, 43 : 11-17
55) 大原甞一郎 : 野兎病の最近の知見. 臨床検査 1971, 15 : 337-341
56) Kitamura S : Pathology of tularemia. Acta Pathol Jpn 1956, 6 : 719-753
57) 館下孝光, 朝隈蓉子, 斎藤孝久ほか : パラフィン切片での蛍光抗体法による組織内梅毒スピロヘータの証明法. Med Technol 1980, 8 : 647-658
58) Lennert K, Feller AC : Histopathology of Non-Hodgkin's Lymphomas, Springer-Verlag, 1992
59) Burke JS, Butler JJ : Malignant lymphoma with a high content of epithelioid histiocytes (Lennert's lymphoma). Am J Clin Pathol 1976, 66 : 1-9
60) Frizzera G, Moran EM, Rappaport H : Angio-immunoblastic lymphadenopathy. Diagnosis and clinical course. Am J Med 1975, 59 : 803-818
61) Lukes RJ, Tindle BH : Immunoblastic lymphadenopathy. A hyperimmune entity resembling Hodgkin's disease. N Engl J Med 1975, 292 : 1-8
62) Poppema S, Kaiserling E, Lennert K : Hodgkin's disease with lymphocytic predominance, nodular type (nodular paragranuloma) and progressively transformed germinal centers-A cytohistological study. Histopathology 1979, 3 : 295-308
63) Kojima M, Nakamura S, Motoori T et al : Progressive transformation of germinal centers : A clinicopathological study of 42 Japanese patients. Int J Surg Pathol 2003, 11 : 101-107
64) Hansmann ML, Fellbaum C, Hui PK et al : Progressive transformation of germinal centers with and without association to Hodgkin's disease. Am J Clin Pathol 1990, 93 : 219-26
65) Osborne BM, Butler JJ, Gresik MV : Progressive transformation of germinal centers : comparison of 23 pediatric patients to the adult population. Mod Pathol 1992, 5 : 135-140
66) Kojima M, Nakamura S, Shimizu K et al : Classical Hodgkin lymphoma occurring in clusters of nodal marginal zone B-lymphocytes in association with progressive transformation of germinal center : A case report. Pathol Res Pract 2003, 199 : 547-550
67) Taddesse-Heath L, Pittaluga S, Sorbara L et al : Marginal zone B-cell lymphoma in children and young adults. Am J Surg Pathol 2003, 27 : 522-531
68) 須知泰山 : 末梢性T細胞腫瘍の多様性-T領域性リンパ腫群を中心に. 日病理会誌 1989, 78-2 : 21-47
69) Kojima M, Nakamura S, Oyama T et al : Autoimmune disease-associated lymphadenopathy with histological appearance of T-zone dysplasia with hyperplastic follicles. A clinicopathological analysis of nine cases. Pathol Res Pract 2001, 197 : 237-244
70) Kojima M, Nakamura S, Itoh H et al : Acute viral lymphadenitis mimicking low-grade peripheral T-cell lymphoma : A clinicopathologic study of nine cases. APMIS 2001, 109 : 419-427
71) Karube K, Ohshima K, Tsuchiya T et al : A "floral" variant of nodal marginal zone lymphoma. Hum Pathol 2005, 36 : 202-206
P.1368 掲載の参考文献
1) 国立がん研究センター : がん情報サービス, 2019年のがん統計予測 https://ganjoho.jp/reg_stat/statistics/stat/short_pred.html (2019年12月閲覧)
2) Harris NL, Jaffe ES, Stein H et al : A revised European-American classification of lymphoid neoplasms : a proposal from the International Lymphoma Study Group. Blood 1994, 84 : 1361-92
3) Jaffe ES, Harris NL, Stein H et al : WHO classification of tumours. Pathology & Genetics tumours of Haematopoietitc and lymphoid tissues, IARC press, Lyon, 2001
4) Swerdlow SH, Campo E, Harris NL et al : WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, IARC Press, 2008
5) Swerdlow SH, Campo E, Harris NL et al : WHO classification of Tumours, Revised 4th ed, IARC Press, 2017
6) Yuda S, Maruyama D, Maeshima AM et al : Influence of the watch and wait strategy on clinical outcomes of patients with follicular lymphoma in the rituximab era. Ann Hematol 2016, 95 : 2017-2022
7) Alizadeh AA, Eisen MB, Davis RE et al : Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling. Nature 2000, 403 : 503-511
8) Wilson WH, Young RM, Schmitz R et al : Targeting B cell receptor signaling with ibrutinib in diffuse large B cell lymphoma. Nat Med 2015, 21 : 922-926
9) Treon SP, Xu L, Yang G et al : MYD88 L265P somatic mutation in Waldenstrom's macroglobulinemia. N Engl J Med 2012, 367 : 826-33
10) Taniguchi K, Takata K, Chuang SS et al : Frequent MYD88 L265P and CD79B Mutations in Primary Breast Diffuse Large B-Cell Lymphoma. Am J Surg Pathol 2016, 40 : 324-34
11) Sakata-Yanagimoto M, Enami T, Yoshida K et al : Somatic RHOA mutation in angioimmunoblastic T cell lymphoma. Nat Genet 2014, 46 : 171-175
12) Watatani Y, Sato Y, Miyoshi H et al : Molecular heterogeneity in peripheral T-cell lymphoma, not otherwise specified revealed by comprehensive genetic profiling. Leukemia 2019, 33 : 2867-2883
13) Carey CD, Gusenleitner D, Lipschitz M et al : Topological analysis reveals a PD-L1-associated microenvironmental niche for Reed-Sternberg cells in Hodgkin lymphoma. Blood 2017, 130 : 2420-2430
14) Miyoshi H, Ohshima K : Epidemiology of malignant lymphoma and recent progress in research on adult T-cell leukemia/lymphoma in Japan. Int J Hematol 2018, 107 : 420-427
16) Oppezzo P, Magnac C, Bianchi S et al : Do CLL B cells correspond to naive or memory B-lymphocytes? Evidence for an active Ig switch unrelated to phenotype expression and Ig mutational pattern in B-CLL cells. Leukemia 2002, 16 : 2438-2446
17) Schnittger S, Bacher U, Haferlach T et al : Development and validation of a real-time quantification assay to detect and monitor BRAFV600E mutations in hairy cell leukemia. Blood 2012, 119 : 3151-3154
18) Mozos A, Royo C, Hartmann E et al : SOX11 expression is highly specific for mantle cell lymphoma and identifies the cyclin D1-negative subtype. Haematologica 2009, 94 : 1555-1562
19) Masir N, Campbell LJ, Goff LK et al : BCL2 protein expression in follicular lymphomas with t (14 ; 18) chromosomal translocations. Br J Haematol 2009, 144 : 716-25
20) Schuler F, Dolken L, Hirt C et al : Prevalence and frequency of circulating t (14 ; 18) -MBR translocation carrying cells in healthy individuals. Int J Cancer 2009, 124 : 958-963
21) Quintanilla-Martinez L, Sander B, Chan JK et al : Indolent lymphomas in the pediatric population : follicular lymphoma, IRF4/MUM1+ lymphoma, nodal marginal zone lymphoma and chronic lymphocytic leukemia. Virchows Arch 2016, 468 : 141-157
22) Schmidt J, Gong S, Marafioti T et al : Genome-wide analysis of pediatric-type follicular lymphoma reveals low genetic complexity and recurrent alterations of TNFRSF14 gene. Blood 2016, 128 : 1101-1111
23) Yoshino T, Takata K, Tanaka T et al : Recent progress in follicular lymphoma. Pathol Int 2018, 68 : 665-676
24) Yoshino T, Miyake K, Ichimura K et al : Increased incidence of follicular lymphoma in the duodenum. Am J Surg Pathol 2000, 24 : 688-693
25) Sato Y, Ichimura K, Tanaka T, Takata K et al : Duodenal follicular lymphomas share common characteristics with mucosa-associated lymphoid tissue lymphomas. J Clin Pathol 2008, 61 : 377-381
26) Takata K, Tanino M, Ennishi D et al : Duodenal follicular lymphoma : comprehensive gene expression analysis with insights into pathogenesis. Cancer Sci 2014, 105 : 608-615
27) Takata K, Okada H, Ohmiya N et al : Primary gastrointestinal follicular lymphoma involving the duodenal second portion is a distinct entity : A multicenter, retrospective analysis in Japan. Cancer Sci 2011, 102 : 1532-1536
28) Tari A, Kitadai Y, Mouri R et al : A watch-andwait policy versus rituximab-combined chemotherapy in Japanese patients with intestinal follicular lymphoma. J Gastroenterol Hepatol 2018, 33 : 1461-1468
29) Schmatz AI, Streubel B, Kretschmer-Chott E et al : Primary follicular lymphoma of the duodenum is a distinct mucosal/submucosal variant of follicular lymphoma : a retrospective study of 63 cases. J Clin Oncol 2011, 29 : 1445-1451
30) Chisholm KM, Mohlman J, Liew M et al : IRF4 translocation status in pediatric follicular and diffuse large B-cell lymphoma patients enrolled in Children's Oncology Group trials. Pediatr Blood Cancer 2019, 66 : e27770
31) Vermeer MH, Willemze R : Recent advances in primary cutaneous B-cell lymphomas. Curr Opin Oncol 2014, 26 : 230-236
34) Copie-Bergman C, Wotherspoon AC, Capella C et al : Gela histological scoring system for post-treatment biopsies of patients with gastric MALT lymphoma is feasible and reliable in routine practice. Br J Haematol 2013, 160 : 47-52
35) Zamboni G, Franzin G, Scarpa A et al : Carcinoma-like signet-ring cells in gastric mucosa-associated lymphoid tissue (MALT) lymphoma. Am J Surg Pathol 1996, 20 : 588-598
36) Piris MA, Onaindia A, Mollejo M : Splenic marginal zone lymphoma. Best Pract Res Clin Haematol 2017, 30 : 56-64
37) Yu SC, Chen SU, Lu W et al : Expression of CD19 and lack of miR-223 distinguish extramedullary plasmacytoma from multiple myeloma. Histopathology. 2011, 58 : 896-905
38) Keddie S, Lunn MP : POEMS syndrome. Curr Opin Neurol 2018, 31 : 551-558
39) Rosado FG, Oliveira JL, Sohani AR et al : Bone marrow findings of the newly described TEMPI syndrome : when erythrocytosis and plasma cell dyscrasia coexist. Mod Pathol 2015, 28 : 367-372
40) Bianchi G, Anderson KC, Harris NL et al : The heavy chain diseases : clinical and pathologic features. Oncology (Williston Park) 2014, 28 : 45-53
41) Nogai H, Dorken B, Lenz G : Pathogenesis of non-Hodgkin's lymphoma. J Clin Oncol 2011, 29 : 1803-1811
42) Morito T, Fujihara M, Asaoku H et al : Serum soluble interleukin-2 receptor level and immunophenotype are prognostic factors for patients with diffuse large B-cell lymphoma. Cancer Sci 2009, 100 : 1255-1260
43) Bohers E, Mareschal S, Bouzelfen A et al : Targetable activating mutations are very frequent in GCB and ABC diffuse large B-cell lymphoma. Genes Chromosomes Cancer 2014, 53 : 144-153
45) Batlle-Lopez A, Gonzalez de Villambrosia S et al : Stratifying diffuse large B-cell lymphoma patients treated with chemoimmunotherapy : GCB/non-GCB by immunohistochemistry is still a robust and feasible marker. Oncotarget 2016, 7 : 18036-18049
46) Hwang HS, Park CS, Yoon DH et al : High concordance of gene expression profiling-correlated immunohistochemistry algorithms in diffuse large B-cell lymphoma, not otherwise specified. Am J Surg Pathol 2014, 38 : 1046-1057
47) Hartmann S, Doring C, Jakobus C et al : Nodular lymphocyte predominant Hodgkin lymphoma and T cell/histiocyte rich large B cell lymphoma--endpoints of a spectrum of one disease? PLoS One 2013, 8 : e78812
48) Lee JH, Jeong H, Choi JW et al : Clinicopathologic significance of MYD88 L265P mutation in diffuse large B-cell lymphoma : a meta-analysis. Sci Rep 2017, 7 : 1785
49) Shi QY, Feng X, Bao W et al : MYC/BCL2 Co-Expression Is a Stronger Prognostic Factor Compared With the Cell-of-Origin Classification in Primary CNS DLBCL. J Neuropathol Exp Neurol 2017, 76 : 942-948
50) Zhou XA, Louissaint A Jr, Wenzel A et al : Genomic Analyses Identify Recurrent Alterations in Immune Evasion Genes in Diffuse Large B-Cell Lymphoma, Leg Type. J Invest Dermatol 2018, 138 : 2365-2376
51) Oyama T, Ichimura K, Suzuki R et al : Senile EBV+ B-cell lymphoproliferative disorders : a clinicopathologic study of 22 patients. Am J Surg Pathol 2003, 27 : 16-26
52) Ohashi A, Kato S, Okamoto A et al : Reappraisal of Epstein-Barr virus (EBV) in diffuse large B-cell lymphoma (DLBCL) : comparative analysis between EBV-positive and EBV-negative DLBCL with EBV-positive bystander cells. Histopathology 2017, 71 : 89-97
53) Yoshino T, Nakamura S, Matsuno Y et al : Epstein-Barr virus involvement is a predictive factor for the resistance to chemoradiotherapy of gastric diffuse large B-cell lymphoma. Cancer Sci 2006, 97 : 163-166
54) Takakuwa T, Tresnasari K, Rahadiani N et al : Cell origin of pyothorax-associated lymphoma : a lymphoma strongly associated with Epstein-Barr virus infection. Leukemia 2008, 22 : 620-627
55) Roschewski M, Wilson WH : Lymphomatoid granulomatosis. Cancer J 2012, 18 : 469-474
56) Mottok A, Wright G, Rosenwald A et al : Molecular classification of primary mediastinal large B-cell lymphoma using routinely available tissue specimens. Blood 2018, 132 : 2401-2405
57) Murase T, Nakamura S, Kawauchi K et al : An Asian variant of intravascular large B-cell lymphoma : clinical, pathological and cytogenetic approaches to diffuse large B-cell lymphoma associated with haemophagocytic syndrome. Br J Haematol 2000, 111 : 826-834
58) Ponzoni M, Ferreri AJ, Campo E et al : Definition, diagnosis, and management of intravascular large B-cell lymphoma : proposals and perspectives from an international consensus meeting. J Clin Oncol 2007, 25 : 3168-3173
59) Yamaguchi M, Seto M, Okamoto M et al : De novo CD5+ diffuse large B-cell lymphoma : a clinicopathologic study of 109 patients. Blood 2002, 99 : 815-821
60) Gupta GK, Jaffe ES, Pittaluga S : A study of PDL1 expression in intravascular large B cell lymphoma : correlation with clinical and pathological features. Histopathology 2019, 75 : 282-286
61) Pan Z, Hu S, Li M, Zhou Y et al : ALK-positive large B-cell lymphoma : A clinicopathologic study of 26 cases with review of additional 108 cases in the literature. Am J Surg Pathol 2017, 41 : 25-38
62) Lopez A, Abrisqueta P : Plasmablastic lymphoma : current perspectives. Blood Lymphat Cancer 2018, 8 : 63-70
63) Rosenthal A, Younes A : High grade B-cell lymphoma with rearrangements of MYC and BCL2 and/or BCL6 : Double hit and triple hit lymphomas and double expressing lymphoma. Blood Rev 2017, 31 : 37-42
64) Riedell PA, Smith SM : Double hit and double expressors in lymphoma : Definition and treatment. Cancer 2018, 124 : 4622-4632
65) Eberle FC, Salaverria I, Steidl C et al : Gray zone lymphoma : chromosomal aberrations with immunophenotypic and clinical correlations. Mod Pathol 2011, 24 : 1586-1597
66) Pilichowska M, Pittaluga S, Ferry JA et al : Clinicopathologic consensus study of gray zone lymphoma with features intermediate between DLBCL and classical HL. Blood Adv 2017, 1 : 2600-2609
67) Tanaka Y, Maeshima AM, Nomoto J et al : Expression pattern of PD-L1 and PD-L2 in classical Hodgkin lymphoma, primary mediastinal large B-cell lymphoma, and gray zone lymphoma. Eur J Haematol 2018, 100 : 511-517
68) Swerdlow SH, Jaffe ES, Brousset P et al : Cytotoxic T-cell and NK-cell lymphomas : current questions and controversies. Am J Surg Pathol 2014, 38 : e60-71
69) Ichimura K, Kagami Y, Suzuki R et al : Phenotypic analysis of peripheral T/NK cell lymphoma : study of 408 Japanese cases with special reference to their anatomical sites. Pathol Int 2003, 53 : 333-344
70) William BM, Armitage JO : International analysis of the frequency and outcomes of NK/T-cell lymphomas. Best Pract Res Clin Haematol 2013, 26 : 23-32
71) Suzuki R, Nakamura S : Malignancies of natural killer (NK) cell precursor : myeloid/NK cell precursor acute leukemia and blastic NK cell lymphoma/leukemia. Leuk Res 1999, 23 : 615-624
72) Oshimi K, Kawa K, Nakamura S et al : NK-cell neoplasms in Japan. Hematology 2005, 10 : 237-245
73) Kimura H, Cohen JI : Chronic Active Epstein-Barr Virus Disease. Front Immunol 2017, 8 : 1867
74) Kimura H, Fujiwara S : Overview of EBV-Associated T/NK-Cell Lymphoproliferative Diseases. Front Pediatr 2019, 6 : 417
75) Okuno Y, Murata T, Sato Y et al : Defective Epstein-Barr virus in chronic active infection and haematological malignancy. Nat Microbiol 2019, 4 : 404-413
76) Firouzi S, Farmanbar A, Nakai K et al : Clonality of HTLV-1-infected T cells as a risk indicator for development and progression of adult T-cell leukemia. Blood Adv 2017, 1 : 1195-1205
77) Cook LB, Fuji S, Hermine O et al : Revised Adult T-Cell Leukemia-Lymphoma International Consensus Meeting Report. J Clin Oncol 2019, 37 : 677-687
78) Kataoka K, Iwanaga M, Yasunaga JI et al : Prognostic relevance of integrated genetic profiling in adult T-cell leukemia/lymphoma. Blood 2018, 131 : 215-225
79) Nakagawa M, Schmitz R, Xiao W et al : Gain-offunction CCR4 mutations in adult T cell leukemia/lymphoma. J Exp Med 2014, 211 : 2497-2505
80) Yoshida N, Miyoshi H, Kato T et al : CCR4 frameshift mutation identifies a distinct group of adult T cell leukaemia/lymphoma with poor prognosis. J Pathol 2016, 238 : 621-626
81) Sakamoto Y, Ishida T, Masaki A et al : CCR4 mutations associated with superior outcome of adult T-cell leukemia/lymphoma under mogamulizumab treatment. Blood 2018, 132 : 758-761
82) Miyoshi H, Kiyasu J, Kato T et al : PD-L1 expression on neoplastic or stromal cells is respectively a poor or good prognostic factor for adult T-cell leukemia/lymphoma. Blood 2016, 128 : 1374-1381
83) Asano N, Miyoshi H, Kato T et al : Expression pattern of immunosurveillance-related antigen in adult T cell leukaemia/lymphoma. Histopathology 2018, 72 : 945-954
84) Asano N, Kato S, Nakamura S : Epstein-Barr virus-associated natural killer/T-cell lymphomas. Best Pract Res Clin Haematol 2013, 26 : 15-21
85) Harabuchi Y, Takahara M, Kishibe K et al : Extranodal Natural Killer/T-Cell Lymphoma, Nasal Type : Basic Science and Clinical Progress. Front Pediatr 2019, 7 : 141.
86) Hamada T, Nakamura S, Ko YH et al : Epstein-Barr virus-associated T/natural killer-cell lymphomas in the elderly : the first consensus meeting in Kofu 2013. J Dermatol 2014, 41 : 40-42
87) Wu CC, Takahashi E, Asano N et al : Primary cutaneous NK/T-cell lymphoma of nasal type : an age-related lymphoproliferative disease? Hum Pathol 2017, 68 : 61-68
88) Hu LM, Takata K, Miyata-Takata T et al : Clinicopathological analysis of 12 patients with Epstein-Barr virus-positive primary intestinal T/natural killer-cell lymphoma (EBV+ ITNKL). Histopathology 2017, 70 : 1052-1063
89) Tanaka T, Yamamoto H, Elsayed AA et al : Clinicopathologic Spectrum of Gastrointestinal T-cell Lymphoma : Reappraisal Based on T-cell Receptor Immunophenotypes. Am J Surg Pathol 2016, 40 : 777-785
90) Willemze R, Cerroni L, Kempf W et al : The 2018 update of the WHO-EORTC classification for primary cutaneous lymphomas. Blood 2019, 133 : 1703-1714
91) Eladl AE, Satou A, Elsayed AA et al : Clinicopathological Study of 30 Cases of Peripheral T-cell Lymphoma with Hodgkin and Reed-Sternberg-like B-cells from Japan. Am J Surg Pathol 2017, 41 : 506-516
92) Sakakibara A, Kohno K, Eladl AE et al : Immunohistochemical assessment of the diagnostic utility of PD-L1 : a preliminary analysis of anti-PD-L1 antibody (SP142) for lymphoproliferative diseases with tumour and non-malignant Hodgkin-Reed-Sternberg (HRS) -like cells. Histopathology 2018, 72 : 1156-1163
93) Yamashita D, Shimada K, Takata K et al : Reappraisal of nodal Epstein-Barr Virus-negative cytotoxic T-cell lymphoma : Identification of indolent CD5+ diseases. Cancer Sci 2018, 109 : 2599-2610
94) Satou A, Asano N, Kato S et al : FoxP3-positive T cell lymphoma arising in non-HTLV1 carrier : clinicopathological analysis of 11 cases of PTCL-NOS and 2 cases of mycosis fungoides. Histopathology 2016, 68 : 1099-1108
95) Kato S, Takahashi E, Asano N et al : Nodal cytotoxic molecule (CM) -positive Epstein-Barr virus (EBV) -associated peripheral T cell lymphoma (PTCL) : a clinicopathological study of 26 cases. Histopathology 2012, 61 : 186-199
96) Kato S, Asano N, Miyata-Takata T et al : T-cell receptor (TCR) phenotype of nodal Epstein-Barr virus (EBV) -positive cytotoxic T-cell lymphoma (CTL) : a clinicopathologic study of 39 cases. Am J Surg Pathol 2015, 39 : 462-471
97) Boi M, Zucca E, Inghirami G et al : Advances in understanding the pathogenesis of systemic anaplastic large cell lymphomas. Br J Haematol 2015, 168 : 771-783
98) Zhang JP, Song Z, Wang HB et al : A novel model of controlling PD-L1 expression in ALK+ anaplastic large cell lymphoma revealed by CRISPR screening. Blood 2019, 134 : 171-185
99) Shen J, Li S, Medeiros LJ et al : PD-L1 expression is associated with ALK positivity and STAT3 activation, but not outcome in patients with systemic anaplastic large cell lymphoma. Mod Pathol 2019
100) Asano N, Oshiro A, Matsuo K et al : Prognostic significance of T-cell or cytotoxic molecules phenotype in classical Hodgkin's lymphoma : a clinicopathologic study. J Clin Oncol 2006, 24 : 4626-4633
101) Asano N, Suzuki R, Matsuo K et al : Cytotoxic molecule expression is predictive of prognosis in Hodgkin's-like anaplastic large cell lymphoma. Histopathology 2007, 50 : 705-715.
102) Venkataraman G, Song JY, Tzankov A et al : Aberrant T-cell antigen expression in classical Hodgkin lymphoma is associated with decreased event-free survival and overall survival. Blood 2013, 121 : 1795-1804
103) Luchtel RA, Dasari S, Oishi N et al : Molecular profiling reveals immunogenic cues in anaplastic large cell lymphomas with DUSP22 rearrangements. Blood 2018, 132 : 1386-1398
104) Wang HW, Balakrishna JP, Pittaluga S et al : Diagnosis of Hodgkin lymphoma in the modern era. Br J Haematol 2019, 184 : 45-59
105) Roemer MG, Advani RH, Ligon AH et al : PDL1 and PD-L2 Genetic Alterations Define Classical Hodgkin Lymphoma and Predict Outcome. J Clin Oncol 2016, 34 : 2690-2697
106) Eladl AE, Satou A, Elsayed AA et al : Nodular lymphocyte predominant Hodgkin lymphoma : Clincopathological study of 25 cases from Japan with a reappraisal of tissue associated macrophages. Pathol Int 2015, 65 : 652-660
107) Natkunam Y, Gratzinger D, Chadburn A et al : Immunodeficiency-associated lymphoproliferative disorders : time for reappraisal? Blood 2018, 132 : 1871-1878
108) Satou A, Tsuzuki T, Nakamura S : Other Iatrogenic Immunodeficiency-Associated Lymphoproliferative Disorders with a T- or NK-cell phenotype. J Clin Exp Hematop 2019, 59 : 56-63
109) Dojcinov SD, Venkataraman G, Raffeld M et al : EBV positive mucocutaneous ulcer--a study of 26 cases associated with various sources of immunosuppression. Am J Surg Pathol 2010, 34 : 405-417
110) Ikeda T, Gion Y, Yoshino T et al : A review of EBV-positive mucocutaneous ulcers focusing on clinical and pathological aspects. J Clin Exp Hematop 2019, 59 : 64-71
111) Daroontum T, Kohno K, Eladl AE et al : Comparison of Epstein-Barr virus-positive mucocutaneous ulcer associated with treated lymphoma or methotrexate in Japan. Histopathology 2018, 72 : 1115-1127
112) Ishikawa E, Kato S, Shimada K et al : Clinicopathological analysis of primary intestinal diffuse large B-cell lymphoma : Prognostic evaluation of CD5, PD-L1, and Epstein-Barr virus on tumor cells. Cancer Med 2018, 7 : 6051-6063
113) Takahashi E, Nakamura S : Histiocytic sarcoma : an updated literature review based on the 2008 WHO classification. J Clin Exp Hematop 2013, 53 : 1-8
114) Kawase T, Hamazaki M, Ogura M et al : CD56/NCAM-positive Langerhans cell sarcoma : a clinicopathologic study of 4 cases. Int J Hematol 2005, 81 : 323-329
115) Sakakibara A, Takahashi E, Ishikawa E et al : Neoplastic PD-L1 expression on interdigitating dendritic cell sarcoma : A supplementary study of a case report. Pathol Int 2018, 68 : 577-578
P.1396 掲載の参考文献
1) Satoh T, Takeda R, Oikawa H et al : Immunohistochemical and structural characteristics of the reticular framework of the white pulp and marginal zone in the human spleen. Anat Rec 1997, 249 : 486-494
2) Kashimura M, Fujita T : A scanning electron microscopy study of human spleen : relationship between the microcirculation and functions. Scanning Microsc 1987, 1 : 841-851
3) Schmidt EE, Macdonald IC, Groom AC : Microcirculatory pathways in normal human spleen, demonstrated by scanning electron microscopy of corrosion casts. Am J Anat 1988, 181 : 253-266
4) Sasou S, Satodate R, Masuda T et al : Scanning electron microscopic features of spleen in the rat and human : a comparative study. Scan Electron Microsc 1986, (Pt 3) : 1063-1069
5) 佐藤孝, 舘道芳徳, 高須修ほか : 脾臓の生理機能と病理-血行動態も含めて. 肝胆膵 2008, 56 : 331-338
6) Parrott DV, De Sousa MA, East J : Thymus-dependent areas in the lymphoid organs of neonatally thymectomized mice. J Exp Med 1966, 123 : 191-204
7) van Krieken JH, von Schilling C, Kluin PM et al : Splenic marginal zone lymphocytes and related cells in the lymph node : a morphologic and immunohistochemical study. Hum Pathol 1989, 20 : 320-325
8) Satoh T : Immunohistochemical observation of the periarteriolar lymphoid sheath, lymph follicle and marginal zone in the 60Co-irradiated spleen of rats. Acta Pathol Jpn 1991, 41 : 581-589
9) 佐藤武彦 : 特発性門脈圧亢進における静脈洞の走査電顕による観察. 日網会誌 1991, 31 : 257-265
10) 白石直人, 佐熊勉, 佐藤孝 : 特発性門脈圧亢進症脾における静脈洞内皮の免疫組織化学的特性. 日網会誌 1994, 34 : 193-203
11) Buckley PJ, Dickson SA, Walker WS : Human splenic sinusoidal lining cells express antigens associated with monocytes, macrophages, endothelial cells, and T lymphocytes. J Immunol 1985, 134 : 2310-2315
12) Crosby WH : Hematology, McGraw-Hill, 1983, 89-97
13) Langley GR, Felderhof CH : Atypical autohemolysis in hereditary spherocytosis as a reflection of two cell populations : relationship of cell lipids to conditioning by the spleen. Blood 1968, 32 : 569-585
14) Satodate R, Suzuki A, Iwasaki T et al : Distribution of blood-borne particles of two different sizes in rat spleens. Virchow Arch Cell Pathol 1986, 51 : 97-105
15) Satoh T, Sakurai E, Tada H et al : Ontogeny of reticular framework of white pulp and marginal zone in human spleen : immunohistochemical studies of fetal spleens from the 17th to 40th week of gestation. Cell Tissue Res 2009, 336 : 287-297
16) 立石一馬, 柳田公佑, 槇野征一郎ほか : 無脾症候群の末梢赤血球の形態異常に関する知見. 医学のあゆみ 1976, 97 : 342-344
17) 円山英昭 : ヒト脾臓の発生と異常. 病理と臨床 1988, 6 : 1396-1405
18) 内藤眞 : Gaucher病とその類縁疾患. 病理と臨床 1986, 4 : 1017-1025
19) 高橋潔 : 先天性ライソソーム病とマクロファージ. 生命を支えるマクロファージ (高橋潔, 内藤眞, 竹屋元裕編), 文光堂, 2001, 328-345
20) 高橋潔 : 代謝疾患と網内系. 現代病理学大系 18B (飯島宗一, 石川英世, 影山圭三ほか編), 中山書店, 1987, 299-341
21) 石原得博, 山下吉美, 高橋睦夫ほか : 脾臓の代謝障害. 病理と臨床 1988, 6 : 1432-1443
22) 今井深, 亀田治男 : 特発性門脈圧亢進症. 肝胆膵 1991, 22 : 519-527
23) 佐藤武彦, 佐藤孝, 笹生俊一ほか : 特発性門脈圧亢進症における脾臓の病理. 肝胆膵 1991, 22 : 619-626
24) Tanaka M, Kanamori H, Fujisawa S et al : Primary splenic Hodgkin's disease with remarkable granulomatous reaction. Leuk Lymphoma 2001, 41 : 225-227
25) Genetics Home Reference. https://ghr.nlm.nih.gov/condition/hereditary-spherocytosis#genes
26) 菊池昌弘, 岩崎宏, 三井徹次他 : 溶血性貧血脾の組織像-光顕レベルの観察. 臨床血液 1981, 22 : 578-584
27) 廣野見 : グルコース-6-リン酸脱水素酵素異常症. 臨床検査 1992, 36 : 223-224
28) 笹生俊一, 高山和夫, 里舘良一 : ITP脾臓の形態. 細胞 1987, 19 : 295-298
29) 佐藤武彦, 佐熊勉, 増田友之ほか : 外傷性脾嚢胞の1例. 岩手医誌 1991, 43 : 327-331
30) O'Malley DP, George T, Orazi A et al : Benign and reactive conditions of lymph node and spleen, American Registry of Pathology, 2009, 523-552
31) Arber DA, Stricker JG, Chen YY et al : Splenic vascular tumors ; a histologic, immunophenotypic, and virologic study. Am J Pathol 1997, 21 : 827-835
32) Martel M, Cheuk W, Lombardi L et al : Sclerosing angiomatoid nodular transformation (SANT) : report of 25 cases of a distinctive benign splenic lesion. Am J Surg Pathol 2004, 28 : 1268-1279
33) Nomura R, Tokumura H, Katayose Y et al : Sclerosing angiomatoid nodular transformation of the spleen : Lessons from a rare case and review of the literature. Inten Med 2019, 58 : 1433-1441
34) Cotelingam JD, Jaffe ES : Inflammatory pseudotumor of the spleen. Am J Surg Pathol 1984, 8 : 375-384
35) 神山隆一, 石川雄一, 北川昌伸 : 血液疾患と脾臓. 病理と臨床 1988, 6 : 1423-1431
36) Hsieh PP, Olsen RJ, O'Malley DP et al : The role of Janus Kinase 2 V617F mutation in extramedullary hematopoiesis of the spleen in neoplastic myeloid disorders. Mod Pathol 2007, 20 : 929-935
37) Harrison CN, Vannucchi AM, Kiladjian J-J et al : Long-term findings from COMFORT-II, a phase 3 study of ruxolitinib vs best available therapy for myelofibrosis. Leukemia 2016, 30 : 1701-1707
38) Falk S, Stutte HJ : Primary malignant lymphoma of the spleen. A morphologic and immunohistochemical analysis of 17 cases. Cancer 1990, 66 : 2612-2619
39) Kraus MD, Fleming MD, Vonderheide RH : The spleen as a diagnostic specimen : a review of 10 years' experience at two tertiary care institutions. Cancer 2001, 91 : 2001-2009
40) Shimizu-Kohno K, Kimura Y, Kiyasu J et al : Malignant lymphoma of the spleen in Japan : A clinicopathological analysis of 115 cases. Pathol Int 2012, 62 : 577-582
41) Campo E, Hrris NL, Matutes E et al : Splenic marginal zone lymphoma. WHO classification of tumours of haematopoietic and lymphoid tissues (Swerdlow SH, Campo E, Harris NL et al eds), IARC Press, 2017, 223-225
42) Chacon JI, Mollejo M, Munoz E at al : Splenic marginal zone lymphoma : Clinical characteristics and prognostic factors in a series of 60 patients. Blood 2002, 100 : 1648-1654
43) Foucar K, Falini B, Stein H : Hairy cell leukaemia. WHO classification of tumours of haematopoietic and lymphoid tissues (Swerdlow SH, Campo E, Harris NL et al eds), IARC Press, 2017, 226-228
44) Turakhia S, Lanigan C, Hamadeh F et al : Immunohistochemistry for BRAF V600E in the differential diagnosis of hairy cell leukemia vs other splenic B-cell lymphomas. Am J Clin Pathol 2015, 144 : 87-93
45) Garlard P, Jaffe ES, Krenacs L et al : Hepatosplenic T-cell lymphoma. WHO classification of tumours of haematopoietic and lymphoid tissues (Swerdlow SH, Campo E, Harris NL et al eds), IARC Press, 2017, 381-382
46) Ohshima K, Haraoka S, Harada N et al : Hepatosplenic γδ T-cell lymphoma : relation to Epstein-Barr virus and activated cytotoxic molecules. Histopathology 2000, 36 : 127-135
47) Weiss LM, Pileri SA, Chan JKC et al : Histiocytic sarcoma. WHO classification of tumours of haematopoietic and lymphoid tissues (Swerdlow SH, Campo E, Harris NL et al eds), IARC Press, 2017, 468-470
48) Willcox TM, Speer RW, Schlinkert RT et al : Hemangioma of the spleen : presentation, diagnosis, and management. J Gastrointest Surg 2000, 4 : 611-613
49) Falk S, Krishnan J, Meis JM : Primary angiosarcoma of the spleen. A clinicopathologic study of 40 cases. Am J Surg Pathol 1993, 17 : 959-970
50) Falk S, Stutte HJ, Frizzera G : Littoral cell angioma : a novel splenic vascular lesion demonstrating histiocytic differentiation. Am J Surg Pathol 1991, 15 : 1023-1033
51) Rosso R, Pauli M, Gianelli U et al : Littoral cell angiosarcoma of the spleen. Case report with immunohistochemical and ultrastructural analysis. Am J Surg Pathol 1995, 19 : 1203-1208
52) Goh BK, Tan YM, Ong HS et al : Intra-abdominal and retroperitoneal lymphangiomas in pediatric and adult patients. World J Surg 2005, 29 : 837-840
53) Strauli P : Haufigkeit und Morphologie der Tumormetastasierung. Die Milz (Lennert K, Harms D eds), Springer-Verlag, 1970, 406-418
P.1440 掲載の参考文献
1) Zambidis ET, Peault B, Park TS et al : Hematopoietic differentiation of human embryonic stem cells progresses through sequential hematoendothelial, primitive, and definitive stages resembling human yolk sac development. Blood 2005, 106 : 860-870
2) Choi JW, Kim Y, Fujino M et al : Hemoglobin F synthesis is not restricted to fetal erythropoietic organs during extramedullary hematopoiesis. Haematologica 2002, 87 : 323-325
3) Foucar K, Viswanatha DS, Wilson CS eds : Non-Neoplastic Disorders of Bone Marrow, Atlas of Nontumor Pathology (Book 6), American Registry of Pathology, 2009, 397-400
4) Sadahira Y, Mori M : Role of the macrophages in erythropoiesis. Pathol Int 1999, 49 : 841-848
5) Arai F, Hirao A, Ohmura M et al : Tie2/angiopoietin-1 signaling regulates hematopoietic stem cell quiescence in the bone marrow niche. Cell 2004, 118 : 149-161
6) 伊藤雅文 : 骨髄. 外科病理マニュアル. 病理と臨床 2008, 26 (臨時増刊号) : 261-266
7) 定平吉都, 是澤里紗, 岡大五ほか : 骨髄. 免疫組織化学 : 診断と治療選択の指針. 病理と臨床 2014, 32 (臨時増刊号) : 240-247
8) Choi JW, Fujino M, Ito M : F-blast is a useful marker for differentiating hypocellular refractory anemia from aplastic anemia. Int J Hematol 2002, 75 : 257-260
9) Wang R, Yoshida K, Toki T et al : Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia. Br J Hematol 2015, 168 : 854-864
10) Iolascon A, Esposito MR, Russo R : Clinical aspects and pathogenesis of congenital dyserythropoietic anemias : from morphology to molecular approach. Hematologica 2012, 97 : 1786-1794
11) Liu W, Ittmann M, Liu J et al : Human parvovirus B19 in bone marrows from adults with acquired immunodeficiency syndrome : a comparative study using in situ hybridization and immunohistochemistry. Hum Pathol 1997, 28 : 760-766
12) Boocock GR, Morrison JA, Popovic M et al : Mutations in SBDS are associated with Shwachman-Diamond syndrome. Nat Genet 2003, 33 : 97-101
13) Donadieu J, Beaupain B, Fenneteau O et al : Congenital neutropenia in the era of genomics : classification, diagnosis, and natural history. Br J Haematol 2017, 179 : 557-574
14) 小林正夫, 溝口洋子, 唐川修平 : 自己免疫性好中球減少症, 自己免疫性血液疾患, 臓器特異的自己免疫疾患. 別冊日本臨牀 免疫症候群 (第2版) I 2015, 300-303
15) Ochs HD, Filipovich AH, Veys P et al : Wiskott-Aldrich syndrome : diagnosis, clinical and laboratory manifestations, and treatment. Biol Blood Marrow Transplant 2009, 15 (Suppl) : 84-90
16) 矢部普正, 矢部みはる, 小島勢二ほか : Fanconi貧血診療の参照ガイド, 平成28年度改訂版, http://zoketsushogaihan.com/file/guideline_H28/09.pdf
17) 伊藤雅文, 市橋亮一, 岩淵英人 : ITPと脾臓. 病理と臨床 2004, 22 : 1272-1275
18) Harrison CN, Bareford D, Butt N et al : Guideline for investigation and management of adults and children presenting with a thrombocytosis. Br J Haematol 2010, 149 : 352-375
19) 小島勢二, 高橋義行, 西尾信博 : 先天性角化不全症診療の参照ガイド, http://zoketsushogaihan.com/file/guideline_H28/10.pdf
20) 中尾眞二, 小島勢二, 大橋春彦 : 再生不良性貧血診療の参照ガイド 2018年改訂, http://zoketsushogaihan.com/file/guideline_H30/02.pdf
21) Thiele J, Kvasnicka HM, Facchetti F et al : European consensus on grading bone marrow fibrosis and assessment of cellularity. Haematologica 2005, 90 : 1128-1132
22) Boehm J : Gelatinous transformation of the bone marrow : the spectrum of underlying diseases. Am J Surg Pathol 2000, 24 : 56-65
23) Hayden A, Park S, Giustini D et al : Hemophagocytic syndromes (HPSs) including hemophagocytic lymphohistiocytosis (HLH) in adults : A systematic scoping review. Blood Rev 2016, 30 : 411-420
24) Naemi K, Brynes RK, Reisian N et al : Benign lymphoid aggregates in the bone marrow : distribution patterns of B and T lymphocytes. Hum Pathol 2012 44 : 512-520
25) Swan N, Skinner M, O'Hara CJ : Bone marrow core biopsy specimens in AL (primary) amyloidosis. A morphologic and immunohistochemical study of 100 cases. Am J Clin Pathol 2003, 120 : 610-616
26) Paydas S, Ergin M, Baslamisli F et al : Bone marrow necrosis : clinicopathologic analysis of 20 cases and review of the literature. Am J Hematol 2002, 70 : 300-305
27) Tefferi A, Guglielmelli P, Larson DR et al : Long-term survival and blast transformation in molecularly annotated essential thrombocythemia, polycythemia vera, and myelofibrosis. Blood 2014, 124 : 2507-2713
28) Chen CJ, Huang YC, Jaing TH et al : Hemophagocytic syndrome : a review of 18 pediatric cases. J Microbiol Immunol Infect 2004, 37 : 157-163
29) Smith MC, Cohen DN, Greig B et al : The ambiguous boundary between EBV-related hemophagocytic lymphohistiocytosis and systemic EBV-driven T cell lymphoproliferative disorder. Int J Clin Exp Pathol 2014, 7 : 5738-5749
30) Kerr JR : A review of blood diseases and cytopenias associated with human parvovirus B19 infection. Rev Med Virol 2015, 25 : 224-240
31) 檜垣克美, 難波栄二 : ライソゾーム病の臨床病理. 病理と臨床 2019, 37 : 175-179
32) Arber DA, Tefferi A, Orazi A et al : Introduction and overview of the classification of myeloid neoplasms. WHO classification of tumours of haematopoietic and lymphoid tissues, Swerdlow SH, Campo E, Harris NL et al eds, IARC, 2017, 16-27
33) Thiele J, Kvasnicka HM, Mullauer L et al : Essential thrombocythemia versus early primary myelofibrosis : a multicenter study to validate the WHO classification. Blood 2011, 117 : 5710-5718
34) 日本血液学会編 : 慢性骨髄性白血病/骨髄増殖性腫瘍 (chronic myeloid leukemia/myeloproliferative neoplasms : CML/MPN), 造血器腫瘍診療ガイドライン 2018年版, 2018, 89-93
35) Maxson JE, Gotlib J, Pollyea DA et al : Oncogenic CSF3R mutations in chronic neutrophilic leukemia and atypical CML. N Engl J Med 2013, 368 : 1781-1790
36) Kralovics R, Passamonti F, Buser AS et al : A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med 2005, 352 : 1779-1790
37) Thiele J, Kvasnicka HM : The 2008 WHO diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis. Curr Hematol Malig Rep 2009, 4 : 33-40
38) Rosati S, Mick R, Xu F et al : Refractory cytopenia with multilineage dysplasia : further characterization of an 'unclassifiable' myelodysplastic syndrome. Leukemia 1996, 10 : 20-26
39) Tefferi A, Thiele J, Orazi A et al : Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis : recommendations from an ad hoc international expert panel. Blood 2007, 110 : 1092-1097
40) Florena AM, Tripodo C, Iannitto E et al : Value of bone marrow biopsy in the diagnosis of essential thrombocythemia. Haematologica 2004, 89 : 911-919
41) Helbig G, Soja A, Bartkowska-Chrobok A et al : Chronic eosinophilic leukemia-not otherwise specified has a poor prognosis with unresponsiveness to conventional treatment and high risk of acute transformation. Am J Hematol 2012, 87 : 643-645
43) Teodosio C, Mayado A, Sanchez-Munoz L et al : The immunophenotype of mast cells and its utility in the diagnostic work-up of systemic mastocytosis. J Leukoc Biol 2015, 97 : 49-59
44) Germing U, Kundgen A, Gattermann N : Risk assessment in chronic myelomonocytic leukemia (CMML). Leuk Lymphoma 2004, 45 : 1311-1318
45) Orazi A, Chiu R, O'Malley DP et al : Chronic myelomonocytic leukemia : The role of bone marrow biopsy immunohistology. Mod Pathol 2006, 19 : 1536-1545
46) Niemeyer CM : JMML genomics and decisions. Hematology Am Soc Hematol Educ Program 2018, 2018 : 307-312
47) Broseus J, Alpermann T, Wulfert et al : Age, JAK2 (V617F) and SF3B1 mutations are the main predicting factors for survival in refractory anaemia with ring sideroblasts and marked thrombocytosis. Leukemia 2013, 27 : 1826-1831
48) 宮崎泰司, 市川幹, 小沢敬也 : 骨髄異形成症候群診療の参照ガイド 平成28年度改訂版, http://zoketsushogaihan.com/file/guideline_H28/04.pdf
49) Tang G, Wang SA, Menon M et al : High-level CD34 expression on megakaryocytes independently predicts an adverse outcome in patients with myelodysplastic syndromes. Leuk Res 2011, 35 : 766-770
50) Verburgh E, Achten R, Louw VJ et al : A new disease categorization of low-grade myelodysplastic syndromes based on the expression of cytopenia and dysplasia in one versus more than one lineage improves on the WHO classification. Leukemia 2007, 21 : 668-677
51) Patnaik MM, Tefferi A : Refractory anemia with ring sideroblasts and RARS with thrombocytosis. Am J Hematol 2015, 90 : 549-559
52) List A, Dewald G, Bennett J et al : Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletion. N Engl J Med 2006, 355 : 1456-1465
53) Kardos G, Baumann I, Passmore SJ et al : Refractory anemia in childhood : a retrospective analysis of 67 patients with particular reference to monosomy 7. Blood 2003, 102 : 1997-2003
54) Iwafuchi H, Ito M : Differences in the bone marrow histology between childhood myelodysplastic syndrome with multilineage dysplasia and refractory cytopenia of childhood without multilineage dysplasia. Histopathology 2019, 74 : 239-247
55) Paschka P, Marcucci G, Ruppert AS et al : Adverse prognostic significance of KIT mutations in adult acute myeloid leukemia with inv (16) and t (8 ; 21) : a Cancer and Leukemia Group B Study. J Clin Oncol 2006, 24 : 3904-3911
56) Marlton P, Keating M, Kantarjian H et al : Cytogenetic and clinical correlates in AML patients with abnormalities of chromosome 16. Leukemia 1995, 9 : 965-971
57) Burnett AK, Russell NH, Hills RK et al : Arsenic trioxide and all-trans retinoic acid treatment for acute promyelocytic leukaemia in all risk groups (AML17) : results of a randomised, controlled, phase 3 trial. Lancet Oncol 2015, 16 : 1295-1305
58) Montesinos P, Rayon C, Vellenga E et al : Clinical significance of CD56 expression in patients with acute promyelocytic leukemia treated with alltrans retinoic acid and anthracycline-based regimens. Blood 2011, 117 : 1799-1805
59) Slovak ML, Gundacker H, Bloomfield CD et al : A retrospective study of 69 patients with t (6 ; 9) (p23 ; q34) AML emphasizes the need for a prospective, multicenter initiative for rare 'poor prognosis' myeloid malignancies. Leukemia 2006, 20 : 1295-1297
60) Secker-Walker LM, Mehta A, Bain B : Abnormalities of 3q21 and 3q26 in myeloid malignancy : a United Kingdom Cancer Cytogenetic Group study. Br J Haematol 1995, 91 : 490-501
61) Bernstein J, Dastugue N, Haas OA et al : Nineteen cases of the t (1 ; 22) (p13 ; q13) acute megakaryblastic leukaemia of infants/children and a review of 39 cases : report from a t (1 ; 22) study group. Leukemia 2000, 14 : 216-218
62) Pasqualucci L, Liso A, Martelli MP et al : Mutated nucleophosmin detects clonal multilineage involvement in acute myeloid leukemia : Impact on WHO classification. Blood 2006, 108 : 4146-4155
63) Mendler JH, Maharry K, Radmacher MD et al : RUNX1 mutations are associated with poor outcome in younger and older patients with cytogenetically normal acute myeloid leukemia and with distinct gene and MicroRNA expression signatures. J Clin Oncol 2012, 30 : 3109-3118
64) Weinberg OK, Seetharam M, Ren L et al : Clinical characterization of acute myeloid leukemia with myelodysplasia-related changes as defined by the 2008 WHO classification system. Blood 2009, 113 : 1906-1908
65) Rowley JD, Olney HJ : International workshop on the relationship of prior therapy to balanced chromosome aberrations in therapy-related myelodysplastic syndromes and acute leukemia : overview report. Genes Chromosomes Cancer 2002, 33 : 331-345
66) Reinig EF, Greipp PT, Chiu A et al : De novo pure erythroid leukemia : refining the clinicopathologic and cytogenetic characteristics of a rare entity. Mod Pathol 2018, 31 : 705-717
67) Inaba H, Zhou Y, Abla O et al : Heterogeneous cytogenetic subgroups and outcomes in childhood acute megakaryoblastic leukemia : a retrospective international study. Blood 2015, 126 : 1575-1584
68) Roy A, Roberts I, Vyas P : Biology and management of transient abnormal myelopoiesis (TAM) in children with Downsyndrome. Semin Fetal Neonatal Med 2012, 17 : 196-201
69) Lange BJ, Kobrinsky N, Barnard DR et al : Distinctive demography, biology, and outcome of acute myeloid leukemia and myelodysplastic syndrome in children with Down syndrome : Children's Cancer Group Studies 2861 and 2891. Blood 1998, 91 : 608-615
70) Hrusak O, Porwit-MacDonald A : Antigen expression patterns reflecting genotype of acute leukemias. Leukemia 2002, 16 : 1233-1258
71) Driessen EM, van Roon EH, Spijkers-Hagelstein JA et al : Frequencies and prognostic impact of RAS mutations in MLL-rearranged acute lymphoblastic leukemia in infants. Haematologica 2013, 98 : 937-944
72) Muhlbacher V, Zenger M, Schnittger S et al : Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93%. Genes Chromosomes Cancer 2014, 53 : 524-536
73) Chiaretti S, Messina M, Foa R : BCR/ABL1-like acute lymphoblastic leukemia : How to diagnose and treat? Cancer 2019, 125 : 194-204
74) You MJ, Medeiros LJ, Hsi ED : T-lymphoblastic leukemia/lymphoma. Am J Clin Pathol 2015, 144 : 411-422
75) Joshi R, Horncastle D, Elderfield K et al : Bone marrow trephine combined with immunohistochemistry is superior to bone marrow aspirate in follow-up of myeloma patients. J Clin Pathol 2008, 61 : 213-216
76) 日本血液学会編 : 慢性リンパ性白血病/小リンパ球性リンパ腫 (CLL/SLL), 造血器腫瘍診療ガイドライン 2018年版, 121-143, 2018
77) Strati P, Shanafelt TD : Monoclonal B-cell lymphocytosis and early-stage chronic lymphocytic leukemia : diagnosis, natural history, and risk stratification. Blood 2015, 126 : 454-462
78) Behdad A, Bailey NG : Diagnosis of splenic B-cell lymphomas in the bone marrow : a review of histopathologic, immunophenotypic, and genetic findings. Arch Pathol Lab Med 2014, 138 : 1295-1301
79) Wotherspoon A, Attygalle A, Mendes LS : Bone marrow and splenic histology in hairy cell leukaemia. Best Pract Res Clin Haematol 2015, 28 : 200-207
80) Matutes E, Martinez-Trillos A, Campo E : Hairy cell leukaemia-variant : Disease features and treatment. Best Pract Res Clin Haematol 2015, 28 : 253-263
81) Kanellis G, Mollejo M, Montes-Moreno S et al : Splenic diffuse red pulp small B-cell lymphoma : revision of a series of cases reveals characteristic clinico-pathological features. Haematologica 2010, 95 : 1122-1129
82) Bassarova A, Troen G, Spetalen S et al : Lymphoplasmacytic lymphoma and marginal zone lymphoma in the bone marrow : paratrabecular involvement as an important distinguishing feature. Am J Clin Pathol 2015, 143 : 797-806
83) Sovani V, Harvey C, Haynes AP et al : Bone marrow trephine biopsy involvement by lymphoma : review of histopathological features in 511 specimens and correlation with diagnostic biopsy, aspirate and peripheral blood findings. J Clin Pathol 2014, 67 : 389-395
84) Hu Z, Li S, Medeiros LJ et al : TCL-1-positive hematogones in a patient with T-cell prolymphocytic leukemia after therapy. Hum Pathol 2017, 65 : 175-179
85) Yabe M, Medeiros LJ, Wang SA et al : Distinguishing Between Hepatosplenic T-cell Lymphoma and γδ T-cell Large Granular Lymphocytic Leukemia : A Clinicopathologic, Immunophenotypic, and Molecular Analysis. Am J Surg Pathol 2017, 41 : 82-93
86) Yang CF, Hsu CY, Ho DM et al : Aggressive natural killer (NK) -cell leukaemia and extranodal NK/T-cell lymphoma are two distinct diseases that differ in their clinical presentation and cytogenetic findings. Histopathology 2018, 72 : 955-964
87) Suzuki K, Suzuki Y, Hama A et al : Recurrent MYB rearrangement in blastic plasmacytoid dendritic cell neoplasm. Leukemia 2017, 31 : 1629-1633
88) Sakamoto K, Katayama R, Asaka R et al : Recurrent 8q24 rearrangement in blastic plasmacytoid dendritic cell neoplasm : association with immunoblastoid cytomorphology, MYC expression, and drug response. Leukemia 2018, 32 : 2590-2603
89) Tzankov A, Kremer M, Leguit R et al : Histiocytic cell neoplasms involving the bone marrow : summary of the workshop cases submitted to the 18th Meeting of the European Association for Haematopathology (EAHP) organized by the European Bone Marrow Working Group, Basel 2016. Ann Hematol 2018, 97 : 2117-2128
90) Orazi A : Histopathology in the diagnosis and classification of acute myeloid leukemia, myelodysplastic syndromes, and myelodysplastic/myeloproliferative diseases. Pathobiology 2007, 74 : 97-114
P.1482 掲載の参考文献
1) Dyck PJ, Thomas PK : Peripheral Neuropathy, 4th ed, Elsevier, 2005
2) 秋口一郎 (監) : カラーアトラス末梢神経の病理, 中外医学社, 2010
3) グレイ/ジロラーミ/ポワリエ (編著), 村山繁雄 (監訳) : エスクロール 基本神経病理学, 西村書店, 2009
4) Arahata K, Ishiura S, Ishiguro T et al : Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide. Nature 1988, 333 : 861-833
5) Okinaka S, Kumagai H, Ebashi S et al : Serum creatine phosphokinase. Activity in progressive muscular dystrophy and neuromuscular diseases. Arch Neurol 1961, 4 : 520-525
6) Nonaka I, Sunohara N, Ishiura S et al : Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation. J Neurol Sci 1981, 51 : 141-155
7) Kobayashi K, Nakahori Y, Miyake M et al : An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature 1998, 394 : 388-392
8) Miyoshi K, Kawai H, Iwasa M et al : Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy. Seventeen cases in eight families including an autopsied case. Brain 1986, 109 : 31-54
9) Ishiura H, Shibata S, Yoshimura J et al : Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease. Nat Genet 2019, 51 : 1222-1232
10) Nishino I, Fu J, Tanji K et al : Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease). Nature 2000, 406 : 906-910
11) Tarui S, Okuno G, Ikura Y et al : Phosphofructokinase deficiency in skeletal muscle. A new type of glycogenosis. Biochem Biophys Res Commun 1965, 19 : 517-523
Online Mendelian Inheritance in Man(TM) (http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=OMIM)
埜中征哉 : 臨床のための筋病理, 第4版増補版, 日本医事新報社, 2014
P.1539 掲載の参考文献
1) 石田剛, 今村哲夫 : 非腫瘍性骨関節疾患の病理, 文光堂, 2003
2) 大塚隆信, 福田国彦, 小田義直 (編) : 骨・軟部腫瘍 : 臨床・画像・病理,改訂版2版, 診断と治療社, 2015
3) 小田義直 (総編集) : 骨・軟部腫瘍, がん診療方針のための病理診断プラクティス, 中山書店, 2013
4) 野島孝之, 小田義直 (編) : 骨腫瘍, 腫瘍病理鑑別診断アトラス, 文光堂, 2016
5) 小田義直 : 第24章 骨・関節, 標準病理学, 医学書院, 2019
6) Unni K, Inwards CY eds : Dahlin's Bone Tumors, 6th edition, Lippincott Williams & Wilkins, Philadelphia, 2010
7) Fletcher CDM, Bridge JA, Hogendoorn PCW et al eds : WHO Classification of Tumours of Soft Tissue and Bone, IARC, 2013
8) Cerniak B eds : Dorfman and Cerniak's Bone Tumors, 2nd edition, Elsevier, 2016
9) Nielsen P, Rosenbuerg A eds : Diagnostic Pathology, Bone, 2nd Edition, Elsevier, 2017
10) Bullough PG : Orthopaedic Pathology, 5th ed., Mosby Elsevier, 2010
11) Klein MJ, Bonar SF, Freemont T et al : Non-Neoplastic Diseases of Bones and Joints, AFIP ARP, 2011
12) 西村玄 : 骨系統疾患X線アトラス, 遺伝性骨疾患の鑑別診断, 医学書院, 1993
13) 骨系統疾患コンソーシウム. http://www2.riken.jp/lab/OA-team/JSDC/about-us.html
14) Folpe AL, Fanburg-Smith JC, Billings SD et al : Most osteomalacia-associated mesenchymal tumors are a single histopathologic entity : an analysis of 32 cases and a comprehensive review of the literature. Am J Surg Pathol 2004, 28 : 1-30
15) Kravets I : Paget's Disease of Bone : Diagnosis and Treatment. Am J Med 2018, 131 : 1298-1303
16) Yamamoto T : Subchondral insufficiency fractures of the femoral head. Clin Orthop Surg 2012, 4 : 173-180
17) Hofmann SR, Kapplusch F, Girschick HJ et al : Chronic Recurrent Multifocal Osteomyelitis (CRMO) : Presentation, Pathogenesis, and Treatment. Curr Osteoporos Rep 2017, 15 : 542-554
18) Nguyen MT, Borchers A, Selmi C et al : The SAPHO syndrome. Semin Arthritis Rheum 2012, 42 : 254-265
19) 平成27年度日本整形外科学会骨軟部腫瘍委員会全国骨腫瘍登録一覧表
20) Kawaguchi K, Oda Y, Miura H et al : Periosteal osteoblastoma of the distal humerus. J Orthop Sci 1998, 3 : 341-345
21) Lucas DR, Unni KK, McLeod RA et al : Osteoblastoma : clinicopathologic study of 306 cases. Hum Pathol 1994, 25 : 117-134
22) Bertoni F, Bacchini P, Donati D et al : Osteoblastoma-like osteosarcoma. The Rizzoli Institute experience. Mod Pathol 1993, 6 : 707-716
23) Hameed M, Mandelker D : Tumor Syndromes Predisposing to Osteosarcoma. Adv Anat Pathol 2018, 25 : 217-222
24) Sangle NA, Layfield LJ : Telangiectatic osteosarcoma. Arch Pathol Lab Med 2012, 136 : 572-576
25) Nakajima H, Sim FH, Bond JR et al : Small cell osteosarcoma of bone. Review of 72 cases. Cancer 1997, 79 : 2095-2106
26) Hansen MF, Seton M, Merchant A et al : Osteosarcoma in Paget's disease of bone. J Bone Miner Res 2006, 21 Suppl 2 : 58-63
27) Sugiura Y, Kanda H, Motoi N et al : Osteosarcoma arising in fibrous dysplasia, confirmed by mutational analysis of GNAS gene. Pathol Res Pract 2018, 214 : 318-324
28) Torres FX, Kyriakos M : Bone infarct-associated osteosarcoma. Cancer 1992, 70 : 2418-2430
29) Choong PF, Pritchard DJ, Rock MG et al : Low grade central osteogenic sarcoma. A long-term followup of 20 patients. Clin Orthop Relat Res 1996, 322 : 198-206
30) Bertoni F, Bacchini P, Fabbri N et al : Osteosarcoma. Low-grade intraosseous-type osteosarcoma, histologically resembling parosteal osteosarcoma, fibrous dysplasia, and desmoplastic fibroma. Cancer 1993, 71 : 338-45
31) Kurt AM, Unni KK, McLeod RA et al : Lowgrade intraosseous osteosarcoma. Cancer 1990, 65 : 1418-1428
32) Yoshida A, Ushiku T, Motoi T et al : Immunohistochemical analysis of MDM2 and CDK4 distinguishes low-grade osteosarcoma from benign mimics. Mod Pathol 2010, 23 : 1279-1288
33) Dujardin F, Binh MB, Bouvier C et al : MDM2 and CDK4 immunohistochemistry is a valuable tool in the differential diagnosis of low-grade osteosarcomas and other primary fibro-osseous lesions of the bone. Mod Pathol 2011, 24 : 624-637
34) Okada K, Frassica FJ, Sim FH et al : Parosteal osteosarcoma. A clinicopathological study. J Bone Joint Surg Am 1994, 76 : 366-378
35) Bertoni F, Bacchini P, Staals EL et al : Dedifferentiated parosteal osteosarcoma : the experience of the Rizzoli Institute. Cancer 2005, 103 : 2373-2382
36) Rose PS, Dickey ID, Wenger DE et al : Periosteal osteosarcoma : long-term outcome and risk of late recurrence. Clin Orthop Relat Res 2006, 453 : 314-317
37) Okada K, Unni KK, Swee RG et al : High grade surface osteosarcoma : a clinicopathologic study of 46 cases. Cancer 1999, 85 : 1044-1054
38) Bridge JA, Nelson M, Orndal C et al : Clonal karyotypic abnormalities of the hereditary multiple exostoses chromosomal loci 8q24.1 (EXT1) and 11p11-12 (EXT2) in patients with sporadic and hereditary osteochondromas. Cancer 1998, 82 : 1657-1663
39) Amary MF, Bacsi K, Maggiani F et al : IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours. J Pathol 2011, 224 : 334-343
40) Mertens F, Moller E, Mandahl N et al : The t (X ; 6) in subungual exostosis results in transcriptional deregulation of the gene for insulin receptor substrate 4. Int J Cancer 2011, 128 : 487-491
41) Meneses MF, Unni KK, Swee RG : Bizarre parosteal osteochondromatous proliferation of bone (Nora's lesion). Am J Surg Pathol 1993, 17 : 691-697
42) Wu CT, Inwards CY, O'Laughlin S et al : Chondromyxoid fibroma of bone : a clinicopathologic review of 278 cases. Hum Pathol 1998, 29 : 438-446
43) Kurt AM, Unni KK, Sim FH et al : Chondroblastoma of bone. Hum Pathol 1989, 20 : 965-976
44) Amary MF, Berisha F, Mozela R et al : The H3F3 K36M mutant antibody is a sensitive and specific marker for the diagnosis of chondroblastoma. Histopathology 2016, 69 : 121-127
45) Bjornsson J, Unni KK, Dahlin DC et al : Clear cell chondrosarcoma of bone. Observations in 47 cases. Am J Surg Pathol 1984, 8 : 223-230
46) Matsuura S, Ishii T, Endo M et al : Epithelial and cartilaginous differentiation in clear cell chondrosarcoma. Hum Pathol 2013, 44 : 237-243
47) Staals EL, Bacchini P, Bertoni F : Dedifferentiated central chondrosarcoma. Cancer 2006, 106 : 2682-2691
48) Chen S, Fritchie K, Wei S et al : Diagnostic utility of IDH1/2 mutations to distinguish dedifferentiated chondrosarcoma from undifferentiated pleomorphic sarcoma of bone. Hum Pathol 2017, 65 : 239-246
49) Nakashima Y, Unni KK, Shives TC et al : Mesenchymal chondrosarcoma of bone and soft tissue. A review of 111 cases. Cancer 1986, 57 : 2444-2453
50) Wang L, Motoi T, Khanin R et al : Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data. Genes Chromosomes Cancer 2012, 51 : 127-139
51) Hauben EI, Jundt G, Cleton-Jansen AM et al : Desmoplastic fibroma of bone : an immunohistochemical study including beta-catenin expression and mutational analysis for beta-catenin. Hum Pathol 2005, 36 : 1025-1030
52) Yamaguchi T, Imada H, Iida S et al : Notochordal tumors : An update on molecular pathology with therapeutic implications. Surg Pathol Clin 10 : 637-656, 2017
53) 石田剛 : 骨腫瘍の病理, 文光堂, 2012
54) 赤木忠厚, 松原 修, 真鍋俊明 : カラーアトラス病理組織の見方と鑑別診断, 第6版, 医歯薬出版, 2018
56) Lal M, Thakur M, Kashyap S : Alkaptonuric ochronosis. Orthopedics 2014, 37 : e1141-e1149
57) Devaney K, Vinh TN, Sweet DE : Synovial hemangioma : a report of 20 cases with differential diagnostic considerations. Hum Pathol 1993, 24 : 737-745
58) Hallel T1, Lew S, Bansal M : Villous lipomatous proliferation of the synovial membrane (lipoma arborescens). J Bone Joint Surg Am 1988, 70 : 264-270
59) Ushijima M, Hashimoto H, Tsuneyoshi M et al : Giant cell tumor of the tendon sheath (nodular tenosynovitis). A study of 207 cases to compare the large joint group with the common digit group. Cancer 1986, 57 : 875-884
60) West RB, Rubin BP, Miller MA et al : A landscape effect in tenosynovial giant-cell tumor from activation of CSF1 expression by a translocation in a minority of tumor cells. Proc Natl Acad Sci U S A 2006, 103 : 690-695
61) Ushijima M, Hashimoto H, Tsuneyoshi M et al : Pigmented villonodular synovitis. A clinicopathologic study of 52 cases. Acta Pathol Jpn 1986, 36 : 317-326
P.1601 掲載の参考文献
1) 久岡正典 : 病理診断に直結した組織学. 3. 軟部結合組織. 病理と臨床 (臨時増刊) 2017, 35 : 36-44
2) Sidossis L, Kajimura S : Brown and beige fat in humans : thermogenic adipocytes that control energy and glucose homeostasis. J Clin Invest 2015, 125 : 478-486
3) Sultan HA, Boyle AA, Sheppard N : Necrotizing fasciitis. BMJ 2012, 345 : e4274
4) Dimino-Emme L, Gurevitch AW : Cutaneous manifestations of disseminated cryptococcosis. J Am Acad Dermatol 1995, 32 : 844-850
5) 玉田勉 : サルコイドーシスの骨・関節・筋肉病変. 日サ会誌 2013, 33 : 35-42
6) Machinami R : Degenerative change of adipose tissue ; the so-called membranous lipodystrophy. Virchows Arch Pathol Anat Histopathol 1990, 416 : 373-374
7) Vigorita VJ : Orthopaedic Pathology, 3rd ed, Wolters Kluwer, 2016, 669-672
8) Vigorita VJ : Orthopaedic Pathology, 3rd ed, Wolters Kluwer, 2016, 672-677
9) 杉本英治 : 関節周囲の嚢胞性病変 : ガングリオンと滑液包炎. 日本医放会誌 1999, 59 : 295-305
11) 矢吹慶, 柴瑛介, 澁谷亮ほか : 原発性リンパ浮腫の1例. 診断病理 2015, 32 : 312-316
12) Fletcher CDM, Bridge JA, Hogendoorn PCW et al (eds) : WHO Classification of Tumours of Soft Tissue and Bone, 4th ed, IARC Press, Lyon, 2013
13) 大塚隆信, 福田国彦, 小田義直 : 骨・軟部腫瘍 臨床・画像・病理, 第2版, 診断と治療社, 2015, 12-31
14) Wei S, Hemderson-Jackson E, Qian X et al : Soft tissue tumor immunohistochemistry update. Illustrative examples of diagnostic pearls to avoid pitfalls. Arch Pathol Lab Med 2017, 141 : 1072-1091
15) 久岡正典 : 分子生物学的手法が求められる病理診断, (5) 骨軟部腫瘍. 臨床病理 2017, 65 : 1028-1037
16) Guillou L, Coindre JM, Bonichon F et al : Comparative study of the National Cancer Institute and French Federation of Cancer Centers Sarcoma Group grading systems in a population of 410 adult patients with soft tissue sarcoma. J Clin Oncol 1997, 15 : 350-362
17) Amin MB, Edge SB, Greene FL et al (eds) : AJCC Cancer Staging Manual, 8th ed, Springer, 2017
18) 日本整形外科学会診療ガイドライン委員会 (編) : 軟部腫瘍治療ガイドライン 2012, 南江堂, 2012, 4-5
19) American Cancer Society : Survival by stage of soft tissue sarcoma. https://www.cancer.org/cancer/soft-tissue-sarcoma/detection-diagnosisstaging/survival-rates.html
20) Ida CM, Wang X, Erickson-Johnson MR et al : Primary retroperitoneal lipoma : a soft tissue pathology heresy? Report of a case with classic histologic, cytogenetics, and molecular genetic features. Am J Surg Pathol 2008, 32 : 951-954
21) Tkachenko A, Ashar HR, Meloni AM et al : Misexpression of disrupted HMGI architectural factors activates alternative pathways of tumorigenesis. Cancer Res 1997, 57 : 2276-2280
22) Noguchi H, Masuda R, Hisaoka M : Multiple symmetric lipomatosis with spindle cell proliferation. Pathol Int 2016, 66 : 311-312
23) Kubota F, Matsuyama A, Shibuya R et al : Desmin-positivity in spindle cells : under-recognized immunophenotype of lipoblastoma. Pathol Int 2013, 63 : 353-357
24) Van Treeck BJ, Fritchie KJ : Updates in spindle cell/pleomorphic lipomas. Semin Diagn Pathol 2019, 36 : 105-111
25) MaCarthy AJ, Chetty R : Tumours composed of fat are no longer a simple diagnosis : an overview of fatty tumours with a spindle cell component. J Clin Pathol 2018, 71 : 483-492
26) Creytens D, Mentzel T, Ferdinande L et al : "Atypical" pleomorphic lipomatous tumor : a clinicopathologic, immunohistochemical and molecular study of 21 cases, emphasizing its relationship to atypical spindle cell lipomatous tumor and suggesting a morphologic spectrum (atypical spindle cell/pleomorphic lipomatous tumor). Am J Surg Pathol 2017, 41 : 1443-1455
27) Laurino L, Furlanetto A, Orvieto E et al : Well-differentiated liposarcoma (atypical lipomatous tumors). Semin Diagn Pathol 2001, 18 : 258-262
28) Henricks WH, Chu YC, Goldblum JR et al : Dedifferentiated liposarcoma : a clinicopathological analysis of 155 cases with a proposal for an expanded definition of dedifferentiation. Am J Surg Pathol 1997, 21 : 271-281
29) Marino-Enriquez A, Fletcher CD, Dal Cin P et al : Dedifferentiated liposarcoma with "homologous" lipoblastic (pleomorphic liposarcoma-like) differentiation : clinicopathologic and molecular analysis of a series suggesting revised diagnostic criteria. Am J Surg Pathol 2010, 34 : 1122-1131
30) Erickson-Johnson MR, Chou MM, Evers BR et al : Nodular fasciitis : a novel model or transient neoplasia induced by MYH9-USP6 gene fusion. Lab Invest 2011, 91 : 1427-1433
31) Hisaoka M, Hashimoto H : Elastofibroma : clonal proliferation with predominant CD34-positive cells. Virchows Arch 2006, 448 : 195-199
32) Kato I, Yoshida A, Ikegami M et al : FOSL1 immunohistochemistry clarifies the distinction between desmoplastic fibroblastoma and fibroma of tendon sheath. Histopathology 2016, 69 : 1012-1020
33) Laskin WB, Lasota J, Fetsch JF et al : Intranodal palisaded myofibroblastoma : Another mesenchymal neoplasm with CTNNB1 (beta-catenin gene) mutations. Clinicopathologic, immunohistochemical, and molecular genetic study of 18 cases. Am J Surg Pathol 2015, 39 : 197-205
34) Marino-Enriquez A, Fletcher CDM : Angiofibroma of soft tissue : clinicopathologic characterization of a distinctive benign fibrovascular neoplasm in a series of 37 cases. Am J Surg Pathol 2012, 36 : 500-508
35) Kasper B, Baumgarten C, Garcia J et al : An update on the management of sporadic desmoid-type fibromatosis : a European Consensus Initiative between Sarcoma PAtients EuroNet (SPAEN) and European Organization for Research and Treatment of Cancer (EORTC) /Soft Tissue and Bone Sarcoma Group (STBSG). Ann Oncol 2017, 28 : 2399-2408
36) Iwasaki T, Yamamoto H, Oda Y : Current update on the molecular biology of cutaneous sarcoma : dermatofibrosarcoma protuberans. Curr Treat Options in Oncol 2019, 20 : 29
37) Salas S, Resseguier N, Blay JY et al : Prediction of local and metastatic recurrence in solitary fibrous tumor : construction of a risk calculator in a multicenter cohort form the French Sarcoma Group (FSG) database. Ann Oncol 2017, 28 : 1979-1987
38) Yamamoto H, Yamaguchi H, Aishima S et al : Inflammatory myofibroblastic tumor versus IgG4-related sclerosing disease and inflammatory pseudotumor : a comparative clinicopathologic study. Am J Surg Pathol 2009, 33 : 1330-1340
39) Mentzel T, Katenkamp D, Fletcher CD : Lowgrade myofibroblatic sarcoma : analysis of 18 cases in the spectrum of myofibroblastic tumors. Am J Surg Pathol 1998, 22 : 1228-1238
40) Liu H, Sukov WR, Ro JY : The t (1 ; 10) (p22 ; q24) TGFBR3/MGEA5 translocation in pleomorphic hyalinizing angiectatic tumor, myxoinflammatory fibroblastic sarcoma, and hemosiderotic fibrolipomatous tumor. Arch Pathol Lab Med 2019, 143 : 212-221
41) Hung YP, Fletcher CDM, Hornick JL : Evaluation of pan-TRK immunohistochemistry in infantile fibrosarcoma, lipofibromatosis-like neural tumour and histological mimics. Histopathology 2018, 73 : 634-644
42) Folpe AL : Fibrosarcoma : a review and update. Histopathology 2014, 64 : 12-25
43) Sioletic S, Dal Cin P, Fletcher CD et al : Well-differentiated and dedifferentiated liposarcomas with prominent myxoid stroma : analysis of 56 cases. Histopathology 2013, 62 : 287-293
44) Doyle LA, Moller E, Dal Cin P et al : MUC4 is a highly sensitive and specific marker for lowgrade fibromyxoid sarcoma. Am J Surg Pathol 2011, 35 : 733-741
45) Folpe AL, Weiss SW, Fletcher CD et al : Tenosynovial giant cell tumors : evidence for a desmin-poisitive dendritic cell subpopulation. Mod Pathol 1998, 11 : 939-944
46) Luzar B, Calonje E : Cutaneous fibrohistiocytic tumours-an update. Histopathology 2010, 56 : 148-165
47) Mentzel T, Wiesner T, Cerroni L et al : Malignant dermatofibroma : clinicopathological, immunohistochemical, and molecular analysis of seven cases. Mod Pathol 2013, 26 : 256-267
48) Jaffer S, Ambrosini-Spaltro A, Mancini AM et al : Neurothekeoma and plexiform fibrohistiocytic tumor : mere histologic resemblance or histogenetic relationship? Am J Surg Pathol 2009, 33 : 905-913
49) Lee J-C, Liang C-E, Fletcher CDM : Giant cell tumor of soft tissue is genetically distinct from its bone counterpart. Mod Pathol 2017, 30 : 728-733
50) Miettinen M : Smooth muscle tumors of soft tissue and non-uterine viscera : biology and prognosis. Mod Pathol 2014, 27 : S17-S29
51) Kraft S, Fletcher CD : Atypical intradermal smooth muscle neoplasms : clinicopathologic analysis of 84 cases and a reappraisal of cutaneous "leiomyosarcoma". Am J Surg Pathol 2011, 35 : 599-607
52) Willis J, Abdul-Karim FW, di Sant'Agnese PA : Extracardiac rhabdomyomas. Semin Diagn Pathol 1994, 11 : 15-25
53) Nascimento AF, Fletcher CD : Spindle cell rhabdomyosarcoma in adults. Am J Surg Pathol 2005, 29 : 1106-1113
54) Agaram NP, Chen CL, Zhang L et al : Recurrent MYOD1 mutations in pediatric and adult sclerosing and spindle cell rhabdomyosarcomas : evidence for a common pathogenesis. Genes Chromosomes Cancer 2014, 53 : 779-787
55) Agaram NP, LaQuaglia MP, Alaggio R et al : MYOD1-mutant spindle cell and sclerosing rhabdomyosarcoma : an aggressive subtype irrespective of age. A reappraisal for molecular classification and risk stratification. Mod Pathol 2019, 32 : 27-36
56) Gulya AJ : The glomus tumor and its biology. Laryngoscope 1993, 103 : 7-15
57) Folpe AL, Fanburg-Smith JC, Miettinen M et al : Atypical and malignant glomus tumors : analysis of 52 cases, with a proposal for the reclassification of glomus tumors. Am J Surg Pathol 2001, 25 : 1-12
58) Mosquera JM, Sboner A, Zhang L et al : Novel NIR143-NOTCH fusions in benign and malignant glomus tumors. Genes Chromosomes Cancer 2013, 52 : 1075-1087
59) Agaimy A, Bieg M, Michal M et al : Recurrent somatic PDGFRB mutations in sporadic infantile/solitary adult myofibromas but not in angioleiomyomas and myopericytomas. Am J Surg Pathol 2017, 41 : 195-203
60) Matsuyama A, Hisaoka, M, Hashimoto H : Angioleiomyoma : a clinicopathologic and immunohistochemical reappraisal with special reference to the correlation with myopericytoma. Hum Pathol 2007, 38 : 645-651
61) North PE : Pediatric vascular tumors and malformations. Surg Pathol Clin 2010, 3 : 455-494
62) Huang SC, Zhang L, Sung YS et al : Frequent FOS gene rearrangements in epithelioid hemangioma : A molecular study of 58 cases with morphologic reappraisal. Am J Surg Pathol 2015, 39 : 1313-1321
63) Kurek KC, Pansuriya TC, van Ruler MA et al : R132C IDH1 mutations are found in spindle cell hemangiomas and not in other vascular tumors or malformations. Am J Pathol 2013, 182 : 1494-1500
64) John I, Folpe AL : Anastomosing hemangiomas arising in unusual locations : A clinicopathologic study of 17 soft tissue cases showing a predilection for the paraspinal region. Am J Surg Pathol 2016, 40 : 1084-1089
65) Griffin N, Khan N, Meirion Thomas J et al : The radiological manifestations of intramuscular haemangiomas in adults : magnetic resonance imaging, computed tomography and ultrasound appearances. Skeletal Radiol 2007, 36 : 1051-1059
66) Putra J, Gupta A : Kaposiform hemangioendothelioma : a review with emphasis on histological differential diagnoses. Pathology 2017, 49 : 356-362
67) Perry KD, Al-Lbraheemi A, Rubin BP et al : Composite hemangioendothelioma with neuroendocrine marker expression : an aggressive variant. Mod Pathol 2017, 30 : 1589-1602
68) Al-Qaderi A, Mansour AT : Pseudomyogenic hemangioendothelioma. Arch Pathol Lab Med 2019, 143 : 763-767
69) Agaram NP, Zhang L, Cotzia P et al : Expanding the spectrum of genetic alterations in pseudomyogenic hemangioendothelioma with recurrent novel ACTB-FOSB gene fusions. Am J Surg Pathol 2018, 42 : 1653-1661
70) Chang Y, Cesarman E, Pessin MS et al : Identification of herpesvirus-like DNA sequences in AIDS-associated Kaposi's sarcoma. Science 1994, 266 : 1865-1869
71) Hisaoka M, Hashimoto H, Iwamasa T : Diagnostic implication of Kaposi's sarcoma-associated herpesvirus with special reference to the distinction between spindle cell hemangioendothelioma and Kaposi's sarcoma. Arch Pathol Lab Med 1998, 122 : 72-76
72) Radu O, Pantanowitz L : Kaposi sarcoma. Arch Pathol Lab Med 2013, 137 : 289-294
73) Shibuya R, Matsuyama A, Shiba E et al : CAMTA1 is a useful immunohistochemical marker for diagnosing epithelioid haemangioendothelioma. Histopathology 2015, 67 : 827-835
74) Antonescu CR, Le Loarer F, Mosquera JM et al : Novel YAP1-TFE3 fusion defines a distinct subset of epithelioid hemangioendothelioma. Genes Chromosomes Cancer 2013, 52 : 775-784
75) Shustef E, Kazlouskaya V, Pietro VG et al : Cutaneous angiosarcoma : a current update. J Clin Pathol 2017, 70 : 917-925
76) McKay KM, Doyle LA, Lazar AJ et al : Expression of ERG, an Ets family transcription factor, distinguishes cutaneous angiosarcoma from histological mimics. Histopathology 2012, 61 : 989-991
77) Cates JM, Rosenberg AE, O'Connell JX et al : Chondroblastoma-like chondroma of soft tissue : an underrecognized variant and its differential diagnosis. Am J Surg Pathol 2001, 25 : 661-666
78) Fang Z, Matsumoto S, Ae K et al : Postradiation soft tissue sarcoma : a multiinstitutional analysis of 14 cases in Japan. J Orthop Sci 2004, 9 : 242-246
79) Fanburg-Smith JC, Bratthauer GL, Miettinen M : Osteocalcin and osteonectin immunoreactivity in extraskeletal osteosarcoma : a study of 28 cases. Hum Pathol 1999, 30 : 32-38
80) Conner JR, Hornick JL : SATB2 is a novel marker of osteoblastic differentiation in bone and soft tissue tumours. Histopathology 2013, 63 : 36-49
81) Yamashita K, Kohashi K, Yamada Y et al : Primary extraskeletal osteosarcoma : a clinicopathological study of 18 cases focusing on MDM2 amplification status. Hum Pathol 2017, 63 : 63-69
82) Makise N, Sekimizu M, Kubo T et al : Extraskeletal osteosarcoma : MDM2 and H3K27me3 analysis of 19 cases suggest disease heterogeneity. Histopathology 2018, 73 : 147-156
85) Liegl-Atzwanger B, Fletcher JA, Fletcher CDM : Gastrointestinal stromal tumors. Virchows Arch 2010, 456 : 111-127
86) Carroll SL : Molecular mechanisms promoting the pathogenesis of Schwann cell neoplasms. Acta Neuropathol 2012, 123 : 321-348
87) Sciot R, Dal Cin P, Hagemeijer A et al : Cutaneous sclerosing perineurioma with cryptic NF2 gene deletion. Am J Surg Pathol 1999, 23 : 849-853
88) Graadt van Roggen JF, McMenamin ME, Belchis DA et al : Reticular perineurioma : a distinctive variant of soft tissue perineurioma. Am J Surg Pathol 2001, 25 : 485-493
90) Fetsch JF, Laskin WB, Hallman JR et al : Neurothekeoma : an analysis of 178 tumors with detailed immunohistochemical data and long-term patient follow-up information. Am J Surg Pathol 2007, 31 : 1103-1114
91) Fetsch JF, Laskin WB, Miettinen M : Nerve sheath myxoma : a clinicopathologic and immunohistochemical analysis of 57 morphologically distinctive, S-100 protein- and GFAP-positive, myxoid peripheral nerve sheath tumors with a predilection for the extremities and a high local recurrence rate. Am J Surg Pathol 2005, 29 : 1615-1624
92) Rodriguez FJ, Folpe AL, Giannini C et al : Pathology of peripheral nerve sheath tumors : diagnostic overview and update on selected diagnostic problems. Acta Neuropathol 2012, 123 : 295-319
93) Asano N, Yoshida A, Ichikawa H et al : Immunohistochemistry for trimethylated H3K27 in the diagnosis of malignant peripheral nerve sheath tumours. Histopathology 2017, 70 : 385-393
94) Pekmezci M, Cuevas-Ocampo AK, Perry A et al : Significance of H3K27me3 loss in the diagnosis of malignant peripheral nerve sheath tumors. Mod Pathol 2017, 30 : 1710-1719
95) Hollmann TJ, Bovee JV, Fletcher CDM : Digital fibromyxoma (superficial acral fibromyxoma) : a detailed characterization of 124 cases. Am J Surg Pathol 2012, 36 : 789-798
96) Delaney D, Diss TC, Presneau N et al : GNAS1 mutations occur more commonly than previously thought in intramuscular myxoma. Mod Pathol 2009, 22 : 718-724
97) McCluggage WG : Recent developments in vulvovaginal pathology. Histopathology 2009, 54 : 156-173
98) Weissferdt A, Kalhor N, Petersson F et al : Ectopic hamartomatous thymoma-New insights into a challenging entity : a clinicopathologic and immunohistochemical study of 9 cases. Am J Surg Pathol 2016, 40 : 1571-1576
99) Miller K, Goodlad JR, Brenn T : Pleomorphic dermal sarcoma. Adverse histologic features predict aggressive behavior and allow distinction from atypical fibroxanthoma. Am J Surg Pathol 2012, 36 : 1317-1326
100) Fanburg-Smith JC, Miettinen M : Angiomatoid "malignant" fibrous histiocytoma : a clinicopathologic study of 158 cases and further exploration of the myoid phenotype. Hum Pathol 1999, 30 : 1336-1343
101) Schaefer IM, Fletcher CDM : Myxoid variant of so-called angiomatoid "malignant fibrous histiocytoma" : clinicopathologic characterization in a series of 21 cases. Am J Surg Pathol 2014, 38 : 816-823
102) Miettinen M, Finnell V, Fetsch JF : Ossifying fibromyxoid tumor of soft parts-a clinicopathologic and immunohistochemical study of 104 cases with long-term follow-up and a critical review of the literature. Am J Surg Pathol 2008, 32 : 996-1005
103) Graham RP, Dry S, Li X et al : Ossifying fibromyxoid tumor of soft parts : a clinicopathologic, proteomic, and genomic study. Am J Surg Pathol 2011, 35 : 1615-1625
104) Rekhi B, Sable M, Jambhekar NA : Histopathological, immunohistochemical and molecular spectrum of myoepithelial tumours of soft tissues. Virchows Arch 2012, 461 : 687-697
105) Hollmann TJ, Hornick JL : INI1-deficient tumors : diagnostic features and molecular genetics. Am J Surg Pathol 2011, 35 : e47-63
106) Shiba E, Matsuyama A, Shibuya R et al : Immunohistochemical and molecular detection of the expression of FGF23 in phosphaturic mesenchymal tumors including the non-phosphaturic variant. Diagn Pathol 2016, 11 : 26
107) Agaimy A, Michal M, Chiosea S et al : Phosphaturic mesenchymal tumors : clinicopathologic, immunohistochemical and molecular analysis of 22 cases expanding their morphologic and immunophenotypic spectrum. Am J Surg Pathol 2017, 41 : 1371-1380
108) Lee JC, Su SY, Changou CA et al : Characterization of NF1-FGFR1- and novel FN1-FGF1 fusion genes in a large series of phosphaturic mesenchymal tumors. Mod Pathol 2016, 29 : 1335-1346
109) Folpe AL, Mentzel T, Lehr HA et al : Perivascular epithelioid cell neoplasms of soft tissue and gynecologic origin : a clinicopathologic study of 26 cases and review of the literature. Am J Surg Pathol 2005, 29 : 1558-1575
110) Hornick JL, Fletcher CD : Sclerosing PEComa : clinicopathologic analysis of a distinctive variant with a predilection for the retroperitoneum. Am J Surg Pathol 2008, 32 : 493-501
111) Folpe AL, Kwiatkowski DJ : Perivascular epithelioid cell neoplasms : pathology and pathogenesis. Hum Pathol 2010, 41 : 1-15
112) Tajima K, Fuyama S, Yamaguchi H et al : Pure monophasic, epithelial synovial sarcoma without a spindle cell component. Histopathology 1999, 34 : 78-81
113) Thway K, Fisher C : Synovial sarcoma : defining features and diagnostic evolution. Ann Diagn Pathol 2014, 18 : 369-380
114) Guillou L, Wadden C, Coindre JM et al : "Proximal-type" epithelioid sarcoma, a distinctive aggressive neoplasm showing rhabdoid features. Clinicopathologic, immunohistochemical, and ultrastructural study of a series. Am J Surg Pathol 1997, 21 : 130-146
115) Stockman DL, Hornick JL, Deavers MT et al : ERG and FLI1 protein expression in epithelioid sarcoma. Mod Pathol 2014, 27 : 496-501
116) Hornick JL, Dal Cin P, Fletcher CDM : Loss of INI1 expression is characteristic of both conventional and proximal-type epithelioid sarcoma. Am J Surg Pathol 2009, 33 : 542-550
117) Jaber OI, Kirby PA : Alveolar soft part sarcoma. Arch Pathol Lab Med 2015, 139 : 1459-1462
118) Stockman DL, Miettinen M, Suster S et al : Malignant gastrointestinal neuroectodermal tumor : clinicopathologic, immunohistochemical, ultrastructural, and molecular analysis of 16 case with a reappraisal of clear cell sarcoma-like tumors of the gastrointestinal tract. Am J Surg Pathol 2012, 36 : 857-868
119) Hisaoka M, Ishida T, Kuo T et al : Clear cell sarcoma of soft tissue : a clinicopathologic, immunohistochemical, and molecular analysis of 33 cases. Am J Surg Pathol 2008, 32 : 452-460
120) Meis-Kindblom JM, Bergh P, Gunterberg B et al : Extraskeletal myxoid chondrosarcoma : a reappraisal of its morphologic spectrum and prognostic factors based on 117 cases. Am J Surg Pathol 1999, 23 : 646-650
121) Harris M, Coyne J, Tariq M et al : Extraskeletal myxoid chondrosarcoma with neuroendocrine differentiation : a pathologic, cytogenetic, and molecular study of a case with a novel translocation t (9 ; 17) (q22 ; q11. 2). Am J Surg Pathol 2000, 24 : 1020-1026
122) Hisaoka M, Okamoto S, Koyama S et al : Microtubule-associated protein-2 and class III beta-tubulin are expressed in extraskeletal myxoid chondrosarcoma. Mod Pathol 2003, 16 : 453-459
123) Adsay V, Cheng J, Athanasian E et al : Primary desmoplastic small cell tumor of soft tissues and bone of the hand. Am J Surg Pathol 1999, 23 : 1408-1413
124) Lae ME, Roche PC, Jin L et al : Desmoplastic small round cell tumor : a clinicopathologic, immunohistochemical, and molecular study of 32 tumors. Am J Surg Pathol 2002, 26 : 823-835
125) Gerald WL, Ladanyi M, de Alava E et al : Clinical, pathologic, and molecular spectrum of tumors associated with t (11 ; 22) (p13 ; q12) : desmoplastic small round-cell tumor and its variants. J Clin Oncol 1998, 16 : 3028-3036
126) Ordonez NG : Desmoplastic small round cell tumor : II : an ultrastructural and immunohistochemical study with emphasis on new immunohistochemical markers. Am J Surg Pathol 1998, 22 : 1314-1327
127) Oda Y, Tsuneyoshi M : Extrarenal rhabdoid tumors of soft tissue : clinicopathological and molecular genetic review and distinction from other soft-tissue sarcomas with rhabdoid features. Pathol Int 2006, 56 : 287-295
128) Burchill SA : Ewing's sarcoma : diagnostic, prognostic, and therapeutic implications of molecular abnormalities. J Clin Pathol 2003, 56 : 96-102
129) Yoshida A, Sekine S, Tsuta K et al : NKX2.2 is a useful immunohistochemical marker for Ewing sarcoma. Am J Surg Pathol 2012, 36 : 993-999
130) Tomlins SA, Palanisamy N, Brenner JC et al : Usefulness of a monoclonal ERG/FLI1 antibody for immunohistochemical discrimination of Ewing family tumors. Am J Clin Pathol 2013, 139 : 771-779
131) Gu M, Antonescu CR, Guiter G et al : Cytokeratin immunoreactivity in Ewing's sarcoma : prevalence in 50 cases confirmed by molecular diagnostic studies. Am J Surg Pathol 2000, 23 : 410-416
132) Llombart-Bosch A, Machado I, Navarro S et al : Histological heterogeneity of Ewing's sarcoma/PNET : an immunohistochemical analysis of 415 genetically confirmed cases with clinical support. Virchows Arch 2009, 455 : 397-411
133) Neuville A, Collin F, Bruneval P et al : Intimal sarcoma is the most frequent primary cardiac sarcoma : clinicopathologic and molecular retrospective analysis of 100 primary cardiac sarcomas. Am J Surg Pathol 2014, 38 : 461-469
134) Dei Tos AP : Classification of pleomorphic sarcomas : where are we now? Histopathology 2006, 48 : 51-62
135) Antonescu CR, Owosho AA, Zhang L et al : Sarcomas with CIC-rearrangements are a distinct pathologic entity with aggressive outcome. A clinicopathologic and molecular study of 115 cases. Am J Surg Pathol 2017, 41 : 941-949
136) Matsuyama A, Shiba E, Umekita Y et al : Clinicopathologic diversity of undifferentiated sarcoma with BCOR-CCNB3 fusion. Analysis of 11 cases with a reappraisal of the utility of immunohistochemistry for BCOR and CCNB3. Am J Surg Pathol 2017, 41 : 1713-1721
P.1621 掲載の参考文献
1) 松橋信行, 藤澤聡郎 : 腹膜疾患. 内科学, 第11版, 矢崎義雄編, 朝倉書店, 2017, 1013-1019
2) Irving JA, Clement PB : Tumors of the peritoneum. Diagnostic histopathology of tumors, 4th ed., Fletcher CDM ed, Elsevier, 2013, 1031-1055
3) Churg A, Cagle PT, Roggli VL : Tumors of the serosal membranes, AFIP atlas of tumor pathology, 4th series, fascicle 3, ARP Press, 2006, 33-82
4) 井内康輝 : 画像と病理像から学ぶ中皮腫アトラス, 篠原出版新社, 2009, 236-246
5) Chung CTS, Santos GDC, Hwang DM et al : FISH assay development for the detection of p16/CDKN2A deletion in malignant pleural mesothelioma. J Clin Pathol 2010, 63 : 630-634
6) Demicco EG, Park MS, Araujo DM et al : Solitary fibrous tumor : a clinicopathological study of 110 cases and proposed risk assessment model. Mod Pathol 2012, 25 : 1298-1306
7) Oslon NJ, Linos K : Dedifferentiated solitary fibrous tumor : a concise review. Arch Pathol Lab Med 2018, 142 : 761-766
8) Schaefer IM, Marino-Enriquez A, Fletcher JA : What is new in gastrointestinal stromal tumor? Adv Anat Pathol 2017, 24 : 259-267
9) Sakurai S, Hasegawa T, Sakuma S et al : Myxoid epithelioid gastrointestinal stromal tumor (GIST) with mast cell infiltrations : a subtype of GIST with mutations of platelet-derived growth factor receptor alpha gene. Hum Pathol 2004, 35 : 1223-1230
10) Folpe AL, Mentzel T, Lehr HA et al : Perivascular epithelioid cell neoplasms of soft tissue and gynecologic origin : a clinicopathologic study of 26 cases and review of the literature. Am J Surg Pathol 2005, 29 : 1558-1575
11) 高橋裕樹 : IgG4関連疾患. 内科学, 第11版, 矢崎義雄編, 朝倉書店, 2017, 1293-1295
12) Kourea HP, Bilsky MH, Leung DHY et al : Subdiaphragmatic and intrathoracic paraspinal malignant peripheral nerve sheath tumors : a clinicopathologic study of 25 patients and 26 tumors. Cancer 1998, 82 : 2191-2203
13) Antonescu CR, Scheithauer BW, Woodruff JM : Tumors of the peripheral nervous system, AFIP atlas of tumor pathology, 4th series, fascicle 19, ARP Press, 2013, 381-474
14) Jo VY, Marino-Enriquez A, Fletcher CDM : Epithelioid rhabdomyosarcoma : clinicopathologic analysis of 16 cases of a morphologically distinct variant of rhabdomyosarcoma. Am J Surg Pathol 2011, 35 : 1523-1530
15) Coindre JM, Hostein I, Maire G et al : Inflammatory malignant fibrous histiocytomas and dedifferentiated liposarcomas : histological review, genomic profile, and MDM2 and CDK4 status favour a single entity. J Pathol 2004, 203 : 822-830
16) 日本泌尿器科学会, 日本病理学会, 日本医学放射線学会, 日本臨床腫瘍学会編 : 精巣腫瘍取扱い規約, 第4版, 金原出版, 2018, 29-31
17) Hasegawa T, Hirose T, Ayala AG et al : Adult neuroblastoma of the retroperitoneum and abdomen : clinicopathologic distinction from primitive neuroectodermal tumor. Am J Surg Pathol 2001, 25 : 918-924
P.1646 掲載の参考文献
1) 松山高明, 曽根浩元 : 心房・心室の解剖 ; 正常心臓解剖の再考. Heart View 2019, 23 : 128-134
2) 真鍋晋 : 半月弁 (弁尖構造・弁輪構造) ・房室弁 ; 正常心臓解剖の再考. Heart View 2019, 23 : 135-141
3) McCarthy KP, Ring L, Rana BS : Anatomy of the mitral valve : understanding the mitral valve complex in mitral regurgitation. Eur J Echocardiograph 2010, 11 : i3-i9
4) Ho SY : Anatomy of the mitral valve. Heart 2002, 88 (Suppl I) : iv5-iv10
5) 松山高明, 井上紳, 池田善彦ほか : 大動脈弁周囲の構造の特徴と心筋分布-経大動脈アプローチによる高周波通電に関連して-. 心電図 2008, 28 : 567-573
6) Sakakibara S, Konno S : Endomyocardial biopsy. Jpn Heart J 1962, 3 : 537-543
7) Cooper LT, Baughman KL, Feldman AM et al : The role of endomyocardial biopsy in the management of cardiovascular disease : a scientific statement from the American Heart Association, the American College of Cardiology, and the European Society of Cardiology. Endorsed by the Heart Failure Society of America and the Heart Failure Association of the European Society of Cardiology. J Am Coll Cardiol 2007, 50 : 1914-1931
8) Leone O, Veinot JP, Angelini A et al : 2011 consensus statement on endomyocardial biopsy from the Association for European Cardiovascular Pathology and the Society for Cardiovascular Pathology. Cardiovasc Pathol 2012, 21 : 245-274
9) Ishibashi-Ueda H, Matsuyama TA, Ohta-Ogo K et al : Significance and value of endomyocardial biopsy based on our own experience. Circ J 2017, 81 : 417-426
10) Uemura A, Morimoto S, Hiramitsu S et al : Histologic diagnostic rate of cardiac sarcoidosis : evaluation of endomyocardial biopsies. Am Heart J 1999, 138 : 299-302
11) Yoshida A, Ishibashi-Ueda H, Yamada N et al : Direct comparison of the diagnostic capability of cardiac magnetic resonance and endomyocardial biopsy in patients with heart failure. Eur J Heart Fail 2013, 15 : 166-175
12) Imaizumi Y, Eguchi K, Imada H et al : Electron microscopy of contact between a monocyte and a multinucleated giant cell in cardiac sarcoidosis. Can J Cardiol 2016, 32 : 1577.e19-20
13) Casella M, Pizzamiglio F, Dello Russo A et al : Feasibility of combined unipolar and bipolar voltage maps to improve sensitivity of endomyocardial biopsy. Circ Arrhythm Electrophysiol 2015, 8 : 625-632
14) Hiramitsu S, Hiroe M, Uemura A et al : National survey of the use of endomyocardial biopsy in Japan. Jpn Circ J 1998, 62 : 909-912
15) 熊本大学医学部附属病院アミロイドーシス診療センター. http://www2.kuh.kumamoto-u.ac.jp/amyloidunit/
16) 信州大学第三内科アミロイドーシス診断支援サービス. http://www.shinshu-u.ac.jp/faculty/medicine/chair/i-3nai/amyloidosis.html
17) Aretz HT : Myocarditis : the Dallas criteria. Hum Pathol 1987, 18 : 619-624
18) 日本循環器学会 : 急性および慢性心筋炎の診断・治療に関するガイドライン (2009年改訂版). http://www.j-circ.or.jp/guideline/pdf/JCS2009_izumi_h.pdf (2019年12月閲覧)
19) Valantine HA, Tazelaar HD, Macoviak J et al : Cardiac sarcoidosis : response to steroids and transplantation. J Heart Transplant 1987, 6 : 244-250
20) Roberts WC, McAllister HA Jr, Ferrans VJ : Sarcoidosis of the heart. A clinicopathologic study of 35 necropsy patients (group 1) and review of 78 previously described necropsy patients (group 11). Am J Med 1977, 63 : 86-108
21) Lagana SM, Parwani AV, Nichols LC : Cardiac sarcoidosis : a pathology-focused review. Arch Pathol Lab Med 2010, 134 : 1039-1046
22) Uemura A, Morimoto S, Hiramitsu S et al : Histopathologic diagnostic rate of cardiac sarcoidosis : evaluation of endomyocardial biopsies. Am Heart J 1999, 138 : 299-302
23) 日本循環器学会. 循環器病ガイドラインシリーズ 2016年度版 : 心臓サルコイドーシスの診療ガイドライン (2016年版). http://www.j-circ.or.jp/guideline/pdf/JCS2016_terasaki_h.pdf (2019年12月閲覧)
24) Maron BJ, Towbin JA, Thiene G et al : Contemporary definitions and classification of the cardiomyopathies : an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee ; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups ; and Council on Epidemiology and Prevention. Circulation 2006, 113 : 1807-1816
25) Elliott P, Andersson B, Arbustini E et al : Classification of the cardiomyopathies : a position statement from the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur Heart J 2008, 29 : 270-276
26) Richardson P, McKenna W, Bristow M et al : Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies. Circulation 1996, 93 : 841-842
27) d'Amati G, Giordano C : Dilated Cardiomyopathy. Cardiovascular Pathology, 4th ed., Buja LM, Butany J eds., Academic Press, 2015, 437-441
28) Paterick TE, Gerber TC, Pradhan SR et al : Left ventricular noncompaction cardiomyopathy : what do we know? Rev Cardiovasc Med 2010, 11 : 92-99
29) Koga Y, Miyamoto T, Ohtsuki T et al : Natural history of hypertrophic cardiomyopathy : Japanese experience. J Cardiol 2001, 37 Suppl 1 : 147-154
30) Iida K, Yutani C, Imakita M et al : Comparison of percentage area of myocardial fibrosis and disarray in patients with classical form and dilated phase of hypertrophic cardiomyopathy. J Cardiol 1998, 32 : 173-180
31) Sliwa K, Hilfiker-Kleiner D, Petrie MC et al : Current state of knowledge on aetiology, diagnosis, management, and therapy of peripartum cardiomyopathy : a position statement from the Heart Failure Association of the European Society of Cardiology Working Group on peripartum cardiomyopathy. Eur J Heart Fail 2010, 12 : 767-778
32) Maisch B, Richter A, Sandmoller A et al : Inflammatory dilated cardiomyopathy (DCMI). Herz 2005, 30 : 535-544
33) Herman DS, Lam L, Taylor MR et al : Truncations of titin causing dilated cardiomyopathy. N Engl J Med 2012, 366 : 619-628
34) Marian AJ, Braunwald E : Hypertrophic cardiomyopathy : Genetics, pathogenesis, clinical manifestations, diagnosis, and therapy. Circ Res 2017, 121 : 749-770
35) Basso C, Thiene G, Carrado D et al : Hypertrophic cardiomyopathy and sudden death in young : pathological evidence of myocardial ischemia. Human Pathol 2000, 31 : 988-998
36) Chan RH, Maron BJ, Olivotto I et al : Prognostic value of quantitative contrast-enhanced cardiovascular magnetic resonance for the evaluation of sudden death risk in patients with hypertrophic cardiomyopathy. Circulation 2014, 130 : 484-495
37) 心筋生検研究会編 : 第III章 心肥大を主病態とする疾患. 診断モダリティとしての心筋病理, 南江堂, 2017, 151-186
38) Corrado D, Basso C, Pilichou K et al : Molecular biology and clinical management of arrhythmogenic right ventricular cardiomyopathy/dysplasia. Heart 2011, 97 : 530-539
39) Perazzolo Marra M, Rizzo S, Bauce B et al : Arrhythmogenic right ventricular cardiomyopathy. Contribution of cardiac magnetic resonance imaging to the diagnosis. Herz 2015, 40 : 600-606
40) Zhang M, Tavora F, Li L et al : Arrhythmogenic right ventricular cardiomyopathy : reassessing the link with the desmosome. Pathology 2012, 44 : 596-604
41) Rizzo S, Pilichou K, Thiene G et al : The changing spectrum of arrhythmogenic (right ventricular) cardiomyopathy. Cell Tissue Res 2012, 348 : 319-323
42) Marcus FI, McKenna WJ, Sherrill D et al : Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia : proposed modification of the Task Force Criteria. Eur Heart J 2010, 31 : 806-814
43) Arbustini E, Weidemann F, Hall JL : Left ventricular noncompaction : a distinct cardiomyopathy or a trait shared by different cardiac diseases? J Am Coll Cardiol 2014, 64 : 1840-1850
44) Seki A, Patel S, Ashraf S et al : Primary endocardial fibroelastosis : an underappreciated cause of cardiomyopathy in children. Cardiovasc Pathol 2013, 22 : 345-350
45) Endo Y, Furuta A, Nishino I : Danon disease : a phenotypic expression of LAMP-2 deficiency. Acta Neuropathol 2015, 129 : 391-398
46) 野呂瀬準, 塩沢英輔, 野呂瀬朋子ほか : 高齢者の心臓におけるATTRアミロイドーシスの臨床病理学的検討. 心臓 2015, 47 : 1397-1404
47) Hamidi Asl L, Liepnieks JJ, Hamidi Asl K et al : Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1. Am J Pathol 1999, 154 : 221-227
48) Quarta CC, Solomon SD, Uraizee I et al : Left ventricular structure and function in transthyretin-related versus light-chain cardiac amyloidosis. Circulation 2014, 29 : 1840-1849
49) Flodrova P, Flodr P, Pika T et al : Cardiac amyloidosis : from clinical suspicion to morphological diagnosis. Pathology 2018, 50 : 261-268
50) Bhogal S, Ladia V, Sitwala P et al : Cardiac Amyloidosis : An updated review with emphasis on diagnosis and future directions. Curr Probl Cardiol 2018, 43 : 10-34
51) Izumiya Y, Takashio S, Oda S et al : Recent advances in diagnosis and treatment of cardiac amyloidosis. J Cardiol 2018, 71 : 135-143
52) 北浦泰, 寺崎文生, 浮村聡 : 膠原病に合併する心筋症. 内科 2005, 95 : 677-688
53) Engle MA, Erlandson M, Smith CH : Late cardiac complications of chronic, severe, refractory anemia with hemochromatosis. Circulation 1964, 30 : 698-705
54) Rajdev A, Groh WJ : Arrhythmias in the muscular dystrophies. Card Electrophysiol Clin 2015, 7 : 303-308
55) Chew K, Carey K, Ho G et al : The relationship of body habitus and respiratory function in Duchenne muscular dystrophy. Respir Med 2016, 119 : 35-40
56) Schade van Westrum SM, Hoogerwaard EM, Dekker L et al : Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy. Neurology 2011, 77 : 62-66
57) Bollen IAE, Ehler E, Fleischanderl K et al : Myofilament remodeling and function is more impaired in peripartum cardiomyopathy compared with dilated cardiomyopathy and ischemic heart disease. Am J Pathol 2017, 187 : 2645-2658
58) Pinto YM, Elliott PM, Arbustini E et al : Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice : a position statement of the ESC working group on myocardial and pericardial diseases. Eur Heart J 2016, 37 : 1850-1858
59) Kamiya CA, Yoshimatsu J, Ikeda T : Peripartum cardiomyopathy from a genetic perspective. Circ J 2016, 80 : 1684-1688
60) Billingham ME, Cary NR, Hammond ME et al : A working formulation for the standardization of nomenclature in the diagnosis of heart and lung rejection : Heart Rejection Study Group. The international Society for Heart Transplantation. J Heart Transplant 1990, 9 : 587-593
61) Stewart S, Winters GL, Fishbein MC et al : Revision of the 1990 working formulation for the standardization of nomenclature in the diagnosis of heart rejection. J Heart Lung Transplant 2005, 24 : 1710-1720
62) Berry GJ, Burke MM, Andersen C et al : The 2013 International Society for Heart and Lung Transplantation Working Formulation for standardization of nomenclature in the pathologic diagnosis of antibody-mediated rejection in heart transplantation. J Heart Lung Transplant 2013, 32 : 1147-1161
63) Szymanska S, Grajkowska W, Pronicki M : Pathologic diagnosis of antibody-mediated rejection in endomyocardial biopsy after heart transplantation based on renewed International Society for Heart and Lung Transplantation criteria. Pol J Pathol 2014, 65 : 176-181
64) Thiene G, Basso C : Pathology and pathogenesis of infective endocarditis in native heart valves. Cardiovasc Pathol 2006, 15 : 256-263
65) Sheppard, MN : Practical Cardiovascular Pathology, 2nd ed., CRC Press, 2011
66) Machida H, Ishibashi-Ueda H, Nakano K et al : A morphologic study of Carpentier-Edwards pericardial xenografts in the mitral position exhibiting primary tissue failure in adults in comparison with Ionescu-Shiley pericardial xenografts. J Thorac Cardiovasc Surg 2001, 122 : 649-655
67) Schweizer-Cagianut M, Salomon F, Hedinger CE et al : Primary adrenocortical nodular dysplasia with Cushing's syndrome and cardiac myxomas. A peculiar familial disease. Virchows Arch A Pathol Anat Histol 1982, 397 : 183-192
68) Carney JA : The complex of myxomas, spotty pigmentation, and endocrine overactivity. Arch Intern Med 1987, 147 : 418-419
69) Terracciano LM, Mhawech P, Suess K et al : Calretinin as a marker for cardiac myxoma. Diagnostic and histogenetic considerations. Am J Clin Pathol 2000, 114 : 754-759
70) Burke A, Virmani R : Pediatric heart tumors. Cardiovasc Pathol 2008, 17 : 193-198
71) Baba Y, Tsuboi Y, Sakiyama K et al : Cardiac papillary fibroelastoma as a cause of recurrent ischemic strokes : the diagnostic value of serial transesophageal echocardiography. Cerebrovascular Dis 2002, 14 : 256-259
72) Syed FF, Mayosi BM : A modern approach to tuberculous pericarditis. Prog Cardiovasc Dis 2007, 50 : 218-236
73) Zhou Y, Tang G, Medeiros LJ et al : Therapy-related myeloid neoplasms following fludarabine, cyclophosphamide, and rituximab (FCR) treatment in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma. Mod Pathol 2012, 25 : 237-245
74) Misawa Y : Immunoglobulin G4-related cardiovascular diseases. Ann Thorac Cardiovasc Surg 2017, 23 : 281-285
75) Bendek M, Ferenc M, Freudenberg N : Post-irradiation pericardial malignant mesothelioma : an autopsy case and review of the literature. Cardiovasc Pathol 2010, 19 : 377-379
76) Tischoff I, Neid M, Neumann V et al : Pathohistological diagnosis and differential diagnosis. Recent Results Cancer Res 2011, 189 : 57-78
77) Attanoos RL, Gibbs AR : Pathology of malignant mesothelioma. Histopathology 1997, 30 : 403-418
78) Chaabane C, Otsuka F, Virmani R et al : Biological responses in stented arteries. Cardiovasc Res 2013, 99 : 353-363
79) Otsuka F, Finn AV, Yazdani SK et al : The importance of the endothelium in atherothrombosis and coronary stenting. Nat Rev Cardiol 2012, 9 : 439-453
80) Hao H, Ishibashi-Ueda H, Tsujimoto M et al : Drug-eluting stent : importance of clinico-pathological correlations. Circ J 2011, 75 : 1548-1558
P.1665 掲載の参考文献
1) Patrick JG, Allard CW : Blood Vessels, Histology for Pathologist, 4th ed., ed. Stacey EM, Wolters Kluwer, 2012, 233-258
2) Roshni D, Steven JF : ISSVA classification. Semin Pediatr Surg 2014, 23 : 158-161
3) Ross R : The pathogenesis of atherosclerosis : a perspective for the 1990s. Nature 1993, 362 : 801-809
4) Stary HC, Chandler AB, Glagov S et al : A definition of initial, fatty streak, and intermediate lesions of atherosclerosis. A report from the Committee on Vascular Lesions of the Council on Arteriosclerosis. American Heart Association. Circulation 1994, 89 : 2462-2478
5) Stary HC, Chandler AB, Dinsmore RE et al : A definition of advanced types of atherosclerotic lesions and a histological classification of atherosclerosis. A report from the Committee on Vascular Lesions of the Council on Arteriosclerosis, American Heart Association. Circulation 1995, 92 : 1355-1374
6) Nakashima Y, Wight NT, Sueishi K : Early atherosclerosis in humans : role of diffuse intimal thickening and extracellular matrix proteoglycans. Cardiovasc Res 2008, 79 : 14-23
7) Walker DI, Bloor K, Williams G et al : Inflammatory aneurysms of the abdominal aorta. Br J Surg 1972, 59 : 609-614
8) Rasmussen TE, Hallett JW Jr : Inflammatory aortic aneurysms. A clinical review with new perspectives in pathogenesis. Ann Surg 1997, 225 : 155-164
9) Kasashima S, Zen Y, Kawashima A et al : A new clinicopathological entity of IgG4-related inflammatory abdominal aortic aneurysm. J Vasc Surg 2009, 49 : 1264-1271
10) 藤崎純, 金子南紀子, 平栗有沙ほか : 左後頭部外傷性仮性動脈瘤の1例. Neurosonology 2018, 31 : 37-41
11) Daily PO, Trueblood HW, Stinson EB et al : Management of acute aortic dissections. Ann Thorac Surg 1970, 10 : 237-247
12) DeBakey ME, McCollum CH, Crawford ES et al : Dissection and dissecting aneurysms of the aorta : twenty-year follow-up of five hundred twenty-seven patients treated surgically. Surgery 1982, 92 : 1118-1134
13) Nakashima Y, Kurozumi T, Sueishi K et al : Dissecting aneurysm : a clinicopathologic and histopathologic study of 111 autopsied cases. Hum Pathol 1990, 21 : 291-296
14) 峰松一夫, 松岡秀樹, 粕谷潤二 : 全国調査の意義と解釈 脳動脈解離の病態と治療法の開発. The Mt. Fuji Workshop on CVD 2011, 29 : 122-125
15) Saw J, Mancini GBJ, Humphries KH : Contemporary review on spontaneous coronary artery dissection. J Am Coll Cardiol 2016, 68 : 297-312
16) 今北正美, 植田初江 : 大動脈疾患 嚢胞性中膜壊死. 日本臨牀 別冊循環器症候群 III 2008 : 374-377
17) Gornik HL, Persu A, Adlam D et al : First international consensus on the diagnosis and management of fibromuscular dysplasia. J Hypertens 2019, 37 : 229-252
18) Harrison EG Jr, McCormack LJ : Pathologica classification of renal arterial disease in renovascular hypertension. Mayo Clin Proc 1971, 46 : 161-167
19) Slavin RE, Gonzalez-Vitale JC : Segmental mediolytic arteritis : a clinical pathologic study. Lab Invest 1976, 35 : 23-29
20) 稲田潔, 池田庸子 : Segmental arterial mediolysis (SAM) 52例の検討-2, 3の問題点について. 病理と臨床 2008, 26 : 185-194
21) Jennette JC, Falk RJ, Bacon PA et al : 2012 Revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthritis Rheum 2013, 65 : 1-11
22) 厚生労働省難治性血管炎に関する調査研究班 : CHCC2012 血管炎分類の日本語訳. https://www.vas-mhlw.org/pdf/results/chcc2012.pdf
23) 高安右人 : 奇異ナル網膜中心血管ノ変化ノ一例. 日眼会誌 1908, 12 : 554-555
24) Nasu T : Takayasu's truncoarteritis. Pulseless disease or aortitis syndrome. Acta Pathol Jpn 1982, 32 Suppl : 117-131
25) Hotchi M : Pathological studies on Takayasu arteritis. Heart Vessels Suppl 1992, 7 : 11-17
26) Stone JR, Bruneval P, Angelini A et al : Consensus statement on surgical pathology of the aorta from the Society for Cardiovascular Pathology and the Association for European Cardiovascular Pathology : I. Inflammatory diseases. Cardiovasc Pathol 2015, 24 : 267-278
27) Murai T, Saito K, Kuroda N et al : Acute aortic dissection due to giant cell arteritis Report of two cases. Acta Pathol Jpn 1989, 39 : 821-826
28) Kussmaul A, Maier R : Uber eine bisher nicht beschriebene eigenth Uliche Arterienerkrankung (Periarteritis nodosa), die mit Morbus Brichtii unf rapid fortschretender allgemeien Muskellahmung einhergeht. Deutsch Arch Klin Med 1866, 1 : 484-517
29) Arkin A : A clinical and pathological study of periarteritis nodosa. A report of five cases, one histologically healed. Am J Pathol 1930, 6 : 401-426
30) 川崎富作 : 指趾の特異的落屑を伴う小児の急性熱性皮膚粘膜淋巴腺症候群 (自験例50例の臨床的観察). アレルギー 1967, 16 : 178-222
31) 増田弘毅, 直江史郎, 田中昇 : 川崎病 (MCLS) における冠状動脈の病理学的研究-特に冠状動脈炎と動脈瘤の形態発生の関連について. 脈管学 1981, 21 : 899-912
32) Takahashi K Oharaseki T, Yokouchi Y : Histopathological aspects of cardiovascular lesions in Kawasaki disease. Int J Rheum Dis 2018, 21 : 31-35
33) Nakazawa D, Masuda S, Tomaru U et al : Pathogenesis and therapeutic interventions for ANCA-associated vasculitis. Nat Rev Rheumatol 2019, 15 : 91-101
34) Di Minno MN, Ambrosino P, Ambrosini F et al : Prevalence of deep vein thrombosis and pulmonary embolism in patients with superficial vein thrombosis : a systematic review and meta-analysis. J Thromb Haemost 2016, 14 : 964-972
P.1729 掲載の参考文献
1) 伊古田勇人, 平戸純子 : 脳腫瘍, 細胞診の実際とトピックス. 病理と臨床 2013, 31 (臨時増刊号) : 234-241
2) Louis DN, Ohgaki H, Wiestler OD et al (eds) : WHO classification of tumours of the central nervous system. Updated 4th edition, IARC, Lyon, 2016
3) Ironside JW, Moss TH, Louis DN et al (eds) : Diagnostic Pathology of Nervous System Tumours, Churchill Livingstone, London, 2002
4) Rhodes RH, Davis RL : An unusual fibro-osseous component in intracranial lesions. Hum Pathol 1978, 9 : 309-319
5) Burger PC, Scheithauer BW (eds) : Calcifying pseudoneoplasm of the neuraxis. AFIP Atlas of Tumor Pathology Series 4, Tumors of the central nervous system, 2007, 495-497
6) Blumcke I, Thom M, Aronica E et al : International consensus classification of hippocampal sclerosis in temporal lobe epilepsy : A Task Force report from the ILAE Commission on Diagnostic Methods. Epilepsia 2013, 54 : 1315-1329
7) 宮田元 : てんかん外科病理診-up-to-date- : 海馬硬化症と皮質異形成のILAE組織分類. 病理と臨床 2015, 33 : 388-394
8) Blumcke I, Thom M, Aronica E et al : The clinicopathologic spectrum of focal cortical dysplasias : A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission. Epilepsia 2011, 52 : 158-174
9) Lennon VA, Kryzer TJ, Pittock SJ et al : IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel. J Exp Med 2005, 202 : 473-477
10) Hardy TA, Chataway J : Tumefactive demyelination : an approach to diagnosis and management. J Neurol Neurosurg Psychiatry 2013, 84 : 1047-1053
11) Fuller GN, Burger PC : Central nervous system. Histology for Pathologists, 4th ed., Mills SE ed., Lippincott Williams and Wilkins, 2012, 295-341
12) AbdelRazek MA, Venna N, Stone JH : IgG4-related disease of the central and peripheral nervous systems. Lancet Neurol 2018, 17 : 183-192
13) Lindstrom KM, Cousar JB, Lopes MB : IgG4-related meningeal disease : clinicopathological fatures and proposal for diagnostic criteria. Acta Neuropathol 2010, 120 : 765-776
14) Swain RS, Tihan T, Horval AE et al : Inflammatory myofibroblastic tumor of the central nervous system and its relationship to inflammatory pseudotumor. Hum Pathol 2008, 39 : 410-419
15) Lui PC, Fan YS, Wong SS et al : Inflammatory pseudotumors of the central nervous system. Hum Pathol 2009, 40 : 1611-1617
16) 日本脳神経外科学会, 日本病理学会 (編) : 脳腫瘍取扱い規約, 第4版, 金原出版, 2018
17) 日本脳腫瘍病理学会 (編) : 脳腫瘍臨床病理カラーアトラス, 第4版, 医学書院, 2017
18) 小森隆司, 廣瀬隆則 (編) : 脳腫瘍, 腫瘍病理鑑別診断アトラス, 文光堂, 2017
19) 中里洋一 (編) : アトラス脳腫瘍病理, 中外医学社, 2017
20) 廣瀬隆則 : WHO中枢神経系腫瘍分類改訂第4版の概要. 病理と臨床 2017, 35 : 402-411
23) Watanabe T, Nobusawa S, Kleihues P et al : IDH1 mutations are early events in the development of astrocytomas and oligodendrogliomas. Am J Pathol 2009, 174 : 1149-1153
24) Yan H, Parsons DW, Jin G et al : IDH1 and IDH2 mutations in gliomas. N Engl J Med 2009, 360 : 765-773
25) Nobusawa S, Watanabe T, Kleihues P et al : IDH1 mutations as molecular signature and predictive factor of secondary glioblastomas. Clin Cancer Res 2009, 15 : 6002-6007
26) Ichimura K, Narita Y, Hawkins CE : Diffusely infiltrating astrocytomas : pathology, molecular mechanisms and markers. Acta Neuropathol 2015, 129 : 789-808
27) Arita H, Narita Y, Yoshida A et al : IDH1/2 mutation detection in gliomas. Brain Tumor Pathol 2015, 32 : 79-89
28) Capper D, Zentgraf H, Balss J et al : Monoclonal antibody specific for IDH1 R132H mutation. Acta Neuropathol 2009, 118 : 599-601
29) Heaphy CM, de Wilde RF, Jiao Y et al : Altered telomeres in tumors with ATRX and DAXX mutations. Science 2011, 333 : 425
30) Jiao Y, Killela PJ, Reitman ZJ et al : Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas. Oncotarget 2012, 3 : 709-722
31) Liu XY, Gerges N, Korshunov A et al : Frequent ATRX mutations and loss of expression in adult diffuse astrocytic tumors carrying IDH1/IDH2 and TP53 mutations. Acta Neuropathol 2012, 124 : 615-625
32) Wiestler B, Capper D, Holland-Letz T et al : ATRX loss refines the classification of anaplastic gliomas and identifies a subgroup of IDH mutant astrocytic tumors with better prognosis. Acta Neuropathol 2013, 126 : 443-451
33) Arita H, Narita Y, Fukushima S et al : Upregulating mutations in the TERT promoter commonly occur in adult malignant gliomas and are strongly associated with total 1p19q loss. Acta Neuropathol 2013, 126 : 267-276
34) Louis DN, Perry A, Burger P et al : International Society of Neuropathology--Haarlem consensus guidelines for nervous system tumor classification and grading. Brain Pathol 2014, 24 : 429-435
35) Sonoda Y, Yokoo H, Tanaka S et al : Practical procedures for the integrated diagnosis of astrocytic and oligodendroglial tumors. Brain Tumor Pathol 2019, 36 : 56-62
36) Brat DJ, Aldape K, Colman H et al : cIMPACTNOW update 3 : recommended diagnostic criteria for "Diffuse astrocytic glioma, IDH-wildtype, with molecular features of glioblastoma, WHO grade IV". Acta Neuropathol 2018, 136 : 805-810
37) 田中伸哉 : びまん性膠腫. 病理と臨床 2017, 35 : 412-421
38) 信澤純人 : 脳腫瘍の分子病理学とパラフィン切片を用いた検索の実際. 病理と臨床 2017, 35 : 453-459
39) Takami H, Yoshida A, Fukushima S et al : Revisiting TP53 Mutations and Immunohistochemistry--A Comparative Study in 157 Diffuse Gliomas. Brain Pathol 2015, 25 : 256-265
40) Kleinschmidt-DeMasters BK, Alassiri AH, Birks DK et al : Epithelioid versus rhabdoid glioblastomas are distinguished by monosomy 22 and immunohistochemical expression of INI-1 but not claudin 6. Am J Surg Pathol 2010, 34 : 341-354
41) Kleinschmidt-DeMasters BK, Aisner DL, Birks DK et al Epithelioid GBMs show a high percentage of BRAF V600E mutation. Am J Surg Pathol 2013, 37 : 685-698
42) Nakajima N, Nobusawa S, Nakata S et al : BRAF V600E, TERT promoter mutations and CDKN2A/B homozygous deletions are frequent in epithelioid glioblastomas : a histological and molecular analysis focusing on intratumoral heterogeneity. Brain Pathol 2018, 28 : 663-673
43) Perry A, Miller CR, Gujrati M et al : Malignant gliomas with primitive neuroectodermal tumor-like components : a clinicopathologic and genetic study of 53 cases. Brain Pathol 2009, 19 : 81-90
44) Korshunov A, Capper D, Reuss D et al : Histologically distinct neuroepithelial tumors with histone 3 G34 mutation are molecularly similar and comprise a single nosologic entity. Acta Neuropathol 2016, 131 : 137-146
45) Hinrichs BH, Newman S, Appin CL et al : Farewell to GBM-O : Genomic and transcriptomic profiling of glioblastoma with oligodendroglioma component reveals distinct molecular subgroups. Acta Neuropathol Commun 2016, 4 : 4
46) Herrlinger U, Jones DTW, Glas M et al : Gliomatosis cerebri : no evidence for a separate brain tumor entity. Acta Neuropathol 2016, 131 : 309-319
47) Louis DN, Giannini C, Capper D et al : cIMPACT-NOW update 2 : diagnostic clarifications for diffuse midline glioma, H3 K27M-mutant and diffuse astrocytoma/anaplastic astrocytoma, IDH-mutant. Acta Neuropathol 2018, 135 : 639-642
48) Bechet D, Gielen GG, Korshunov A et al : Specific detection of methionine 27 mutation in histone 3 variants (H3K27M) in fixed tissue from high-grade astrocytomas. Acta Neuropathol 2014, 128 : 733-741
49) Bender S, Tang Y, Lindroth AM et al : Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomas. Cancer Cell 2013, 24 : 660-672
50) Venneti S, Garimella MT, Sullivan LM et al : Evaluation of histone 3 lysine 27 trimethylation (H3K27me3) and enhancer of Zest 2 (EZH2) in pediatric glial and glioneuronal tumors shows decreased H3K27me3 in H3F3A K27M mutant glioblastomas. Brain Pathol 2013, 23 : 558-564
51) Reifenberger J, Reifenberger G, Liu L et al : Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p. Am J Pathol 1994, 145 : 1175-1190
52) Cairncross JG, Ueki K, Zlatescu MC et al : Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas. J Natl Cancer Inst 1998, 90 : 1473-1479
53) Natte R, van Eijk R, Eilers P et al : Multiplex ligation-dependent probe amplification for the detection of 1p and 19q chromosomal loss in oligodendroglial tumors. Brain Pathol 2005, 15 : 192-197
54) Sahm F, Reuss D, Koelsche C et al : Farewell to oligoastrocytoma : in situ molecular genetics favor classification as either oligodendroglioma or astrocytoma. Acta Neuropathol 2014, 128 : 551-559
55) Collins VP, Jones DT, Giannini C : Pilocytic astrocytoma : pathology, molecular mechanisms and markers. Acta Neuropathol 2015, 129 : 775-788
56) Rodriguez FJ, Scheithauer BW, Burger PC et al : Anaplasia in pilocytic astrocytoma predicts aggressive behavior. Am J Surg Pathol 2010, 34 : 147-160
57) Johnson MW, Eberhart CG, Perry A et al : Spectrum of pilomyxoid astrocytomas : intermediate pilomyxoid tumors. Am J Surg Pathol 2010, 34 : 1783-1791
58) Kleinschmidt-DeMasters BK, Donson AM, Vogel H et al : Pilomyxoid astrocytoma (PMA) shows significant differences in gene expression vs. pilocytic astrocytoma (PA) and variable tendency toward maturation to PA. Brain Pathol 2015, 25 : 429-440
59) Phi JH, Park SH, Chae JH et al : Congenital subependymal astrocytoma : clinical considerations and expression of radial glial cell markers in giant cells. Childs Nerv Syst 2008, 24 : 1499-1503
60) Hewer E, Vajtai I : Consistent nuclear expression of thyroid transcription facto 1 in subependymal giant cell astrocytomas suggests lineage-restricted histogenesis. Clin Neuropathol 2015, 34 : 128-131
61) Ida CM, Rodriguez FJ, Burger PC et al : Pleomorphic xanthoastrocytoma : Natural history and long-term follow-up. Brain Pathol 2015, 25 : 575-586
62) Reifenberger G, Kaulich K, Wiestler OD et al : Expression of the CD34 antigen in pleomorphic xanthoastrocytomas. Acta Neuropathol 2003, 105 : 358-364
63) Schindler G, Capper D, Meyer J et al : Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma. Acta Neuropathol 2011, 121 : 397-405
64) Giannini C, Scheithauer BW, Burger PC et al : Pleomorphic xanthoastrocytoma. Cancer 1999, 85 : 2033-2045
65) Hirose T, Ishizawa K, Sugiyama K et al : Pleomorphic xanthoastrocytoma : a comparative pathologic study between conventional and anaplastic types. Histopathology 2008, 52 : 183-193
66) Schmidt Y, Kleinschmidt-DeMasters BK, Aisner DL et al : Anaplastic PXA in adults : case series with clinicopathologic and molecular features. J Neurooncol 2013, 111 : 59-69
67) 佐々木惇 : 上衣系腫瘍. 病理と臨床 2017, 35 : 429-433
68) Kawano N, Ohba Y, Nagashima K : Eosinophilic inclusions in ependymoma represent microlumina : a light and electron microscopic study. Acta Neuropathol 2000, 99 : 214-218
69) Preusser M, Budka H, Rossler K et al : OLIG2 is a useful immunohistochemical marker in differential diagnosis of clear cell primary CNS neoplasms. Histopathology 2007, 50 : 365-370
70) Ishizawa K, Komori T, Shimada S et al : Olig2 and CD99 are useful negative markers for the diagnosis of brain tumors. Clin Neuropathol 2008, 27 : 118-128
71) Kawano N, Yada K, Aihara M et al : Oligodendroglioma-like cells (clear cells) in ependymoma. Acta Neuropathol 1983, 62 : 141-144
72) Hirato J, Nakazato Y, Iijima M et al : An usual variant of ependymoma with extensive tumor cell vacuolization. Acta Neuropathol 1997, 93 : 310-316
73) Vajtai I, Mucs Z, Varga Z et al : Signet-ring cell ependymoma : case report with implications for pathogenesis and differential diagnosis. Pathol Res Pract 1999, 195 : 853-858
74) Ruchoux MM, Kepes JJ, Dhellemmes P et al : Lipomatous differentiation in ependymomas : a report of three cases and comparison with similar changes reported in other central nervous system neoplasms of neuroectodermal origin. Am J Surg Pathol 1998, 22 : 338-346
75) Mezmezian MB, Del Cano V, Olvi LG : Report of a case of giant cell ependymoma with unusual clinical and pathological presentation. Neuropathology 2019, 39 : 313-318
76) Parker M, Mohankumar KM, Panchihewa C et al : C11orf95-RELA fusions drive oncogenic NF-κB signaling in ependymoma. Nature 2014, 506 : 451-455
77) Pajtler KW, Witt H, Sill M et al : Molecular classification of ependymal tumors across all CNS compartments, histological grades, and age groups. Cancer Cell 2015, 27 : 728-743
78) Sasaki A, Hirato J, Hirose T et al : Reviews of ependymomas : assessment of consensus in pathological diagnosis and correlation with genetic profiles and outcome. Brain Tum Pathol 2019, 6 : 92-101
79) Bielle F, Villa C, Giry M et al : Chordoid gliomas of the third ventricle share TTF-1 expression with organum vasculosum of the lamina terminalis. Am J Surg Pathol 2015, 39 : 948-956
80) Preusser M, Hoischen A, Novak K et al : Angiocentric glioma : report of clinico-pathologic and genetic findings in 8 cases. Am J Surg Pathol 2007, 31 : 1709-1718
81) Lehman NL, Hattab EM, Mobley BC et al : Morphological and molecular features of astroblastoma, including BRAF V600E mutations, suggest an ontological relationship to other cortical-based gliomas of children and young adults. Neuro-oncol 2017, 19 : 31-42
82) Hirose T, Nobusawa S, Sugiyama K et al : Astroblastoma : A distinct tumor entity characterized by alterations of the X chromosome and MN1 rearrangement. Brain Pathol 2018, 28 : 684-694
83) Jeibmann A, Hasselblatt M, Gress J et al : Prognostic implications of atypical histologic features in choroid plexus papilloma. J Neuropathol Exp Neurol 2006, 65 : 1069-1073
84) Judkins AR, Burger PC, Hamilton RL et al : INI1 protein expression distinguishes atypical teratoid/rhabdoid tumor from choroid plexus carcinoma. J Neuropathol Exp Neurol 2005, 64 : 391-397
85) Komori T, Arai N : Dysembryoplastic neuroepithelial tumor, a pure glial tumor? Immunohistochemical and morphometric studies. Neuropathology 2013, 33 : 459-468
86) Chappe C, Padovani L, Scavarda D et al : Dysembryoplastic neuroepithelial tumors share with pleomorphic xanthoastrocytomas and gangliogliomas BRAF V600E mutation and expression. Brain Pathol 2013, 23 : 574-583
87) Matsumura N, Nobusawa S, Ito J et al : Multiplex ligation-dependent probe amplification analysis is useful for detecting a copy number gain of the FGFR1 tyrosine kinase domain in dysembryoplastic neuroepithelial tumors. J Neurooncol 2019, 143 : 27-33
88) Huse JT, Edgar M, Halliday J et al : Multinodular and vacuolating neuronal tumors of the cerebrum : 10 cases of a distinctive seizure-associated lesion. Brain Pathol 2013, 23 : 515-524
89) Komori T, Scheithauer BW, Anthony DC et al : Papillary glioneuronal tumor : a new variant of mixed neuronal-glial neoplasm. Am J Surg Pathol 1998, 22 : 1171-1183
90) Tanaka Y, Yokoo H, Komori T et al : A distinct pattern of Olig2-positive cellular distribution in papillary glioneuronal tumors : a manifestation of the oligodendroglial phenotype? Acta Neuropathol 2005, 110 : 39-47
91) Bridge JA, Liu XQ, Sumegi J et al : Identification of a novel, recurrent SLC44A1-PRKCA fusion in papillary glioneuronal tumor. Brain Pathol 2013, 23 : 121-128
92) Komori T, Scheithauer BW, Hirose T : A rosette-forming glioneuronal tumor of the fourth ventricle : infratentorial form of dysembryoplastic neuroepithelial tumor? Am J Surg Pathol 2002, 26 : 582-591
93) Kitamura Y, Komori T, Shibuya M et al : Comprehensive genetic characterization of rosette-forming glioneuronal tumors : independent component analysis by tissue microdissection. Brain Pathol 2018, 28 : 87-93
94) Deng MY, Sill M, Chiang J et al : Molecularly defined diffuse leptomeningeal glioneuronal tumor (DLGNT) comprises two subgroups with distinct clinical and genetic features. Acta Neuropathol 2018, 136 : 239-253
95) Yokoo H, Nobusawa S, Takebayashi H et al : Anti-human Olig2 antibody as a useful immunohistochemical marker of normal oligodendrocytes and gliomas. Am J Pathol 2004, 164 : 1717-1725
96) Brat DJ, Scheithauer BW, Eberhart CG et al : Extraventricular neurocytomas : pathologic features and clinical outcome. Am J Surg Pathol 2001, 25 : 1252-1260
97) Fevre-Montange M, Szathmari A, Champier J et al : Pineocytoma and pineal parenchymal tumors of intermediate differentiation presenting cytologic pleomorphism : a multicenter study. Brain Pathol 2008, 18 : 354-359
98) Jouvet A, Saint-Pierre G, Fauchon F et al : Pineal parenchymal tumors : a correlation of histological features with prognosis in 66 cases. Brain Pathol 2000, 10 : 49-60
99) Jouvet A, Fauchon F, Liberski P et al : Papillary tumor of the pineal region. Am J Surg Pathol 2003, 27 : 505-512
100) Heim S, Sill M, Jones DT et al : Papillary tumor of the pineal region : A distinct molecular entity. Brain Pathol 2016, 26 : 199-205
101) 平戸純子 : 胎児性腫瘍. 病理と臨床 2017, 35 : 444-452
102) Taylor MD, Northcott PA, Korshunov A et al : Molecular subgroups of medulloblastoma : the current consensus. Acta Neuropathol 2012, 123 : 465-472
103) Goschzik T, Zur Muhlen A, Kristiansen G et al : Molecular stratification of medulloblastoma : comparison of histological and genetic methods to detect Wnt activated tumours. Neuropathol Appl Neurobiol 2015, 41 : 135-144
104) Kaur K, Kakker A, Kumar A et al : Integrating molecular subclassification of medulloblastoma into routine clinical practice : A simplified approach. Brain Pathol 2016, 26 : 334-343
105) Zhukova N, Ramaswamy V, Renke M et al : Subgroup-specific prognostic implications of TP53 mutation in medulloblastoma. J Clin Oncol 2013, 31 : 2927-2935
106) Eberhart CG, Brat DJ, Cohen KJ et al : Pediatric neuroblastic brain tumors containing abundant neuropil and true rosettes. Pediatr Dev Pathol 2000, 3 : 346-352
107) Korshunov A, Remke M, Gessi M et al : Focal genomic amplification at 19q13.42 comprises a powerful diagnostic marker for embryonal tumors with ependymoblastic rosettes. Acta Neuropathol 2010, 120 : 253-260
108) Nobusawa S, Yokoo H, Hirato J et al : Analysis of chromosome 19q13.42 amplification in embryonal brain tumors with ependymoblastic multilayered rosettes. Brain Pathol 2012, 22 : 689-697
109) Korshunov A, Sturm D, Ryzhova M et al : Embryonal tumor with abundant neuropil and true rosettes (ETANTR), ependymoblastoma, and medulloepithelioma share molecular similarity and comprise a single clinicopathological entity. Acta Neuropathol 2014, 128 : 279-289
110) Korshunov A, Ryzhova M, Jones DT et al : LIN28A immunoreactivity is a potent diagnostic marker of embryonal tumor with multilayered rosettes (ETMR). Acta Neuropathol 2012, 124 : 875-881
111) Schneppenheim R, Fruhwald MC, Gesk S et al : Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome. Am J Hum Genet 2010, 86 : 279-284
112) Hasselblatt M, Gesk S, Oyen F et al Nonsense mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI1) expression. Am J Surg Pathol 2011, 35 : 933-935
113) Nakata S, Nobusawa S, Hirose T et al : Sellar atypical teratoid/rhabdoid tumor (AT/RT) : a clinicopathologically and genetically distinct variant of AT/RT. Am J Surg Pathol 2017, 41 : 932-940
114) Judkins AR, Mauger J, Ht A et al : Immunohistochemical analysis of hSNF5/INI1 in pediatric CNS neoplasms. Am J Surg Pathol 2004, 28 : 644-650
115) Sturm D, Orr BA, Toprak UH et al : New brain tumor entities emerge from molecular classification of CNS-PNETs. Cell 2016, 164 : 1060-1072
116) Yoshida Y, Nobusawa S, Nakata S et al : CNS high-grade neuroepithelial tumor with BCOR internal tandem duplication : a comparison with its conterparts in the kidney and soft tissue. Brain Pathol 2018, 28 : 710-720
117) Ferris SP, Velazquez Vega J, Aboian M et al : High-grade neuroepithelial tumor with BCOR exon 15 internal tandem duplication-a comprehensive clinical, radiographic, pathologic, and genomic analysis. Brain Pathol 2020, 30 : 46-62
118) Yokoo H, Arai H, Isoda K et al : Characterization of eosinophilic hyaline droplets in schwannoma. Acta Neuropathol 2003, 105 : 170-176
119) Clark VE, Erson-Omay EZ, Serin A et al : Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO. Science 2013, 339 : 1077-1080
120) Reuss DE, Piro RM, Jones DT et al : Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutations. Acta Neuropathol 2013, 125 : 351-358
121) Vaubel RA, Chen SG, Raleigh DR et al : Meningiomas with rhabdoid features lacking other histologic features of malignancy : a study of 44 cases and review of the literature. J Neuropathol Exp Neurol 2016, 75 : 44-52
122) Schweizer L, Koelsche C, Sahm F et al Meningeal hemangiopericytoma and solitary fibrous tumors carry the NAB2-STAT6 fusion and can be diagnosed by nuclear expression of STAT6 protein. Acta Neuropathol 2013, 125 : 651-658
123) Wang L, Motoi T, Khanin R et al : Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data. Genes Chromosomes Cancer 2012, 51 : 127-139
124) Vujovic S, Henderson S, Presneau N et al : Brachyury, a crucial regulator of notochordal development, is a novel biomarker for chordomas. J Pathol 2006, 209 : 157-165
126) Haroche J, Charlotte F, Arnaud L et al : High prevalence of BRAF V600E mutations in Erdheim-Chester disease but not in other non-Langerhans cell histiocytoses. Blood 2012, 120 : 2700-2703
127) Techavichit P, Sosothikul D, Chaichana T et al : BRAF V600E mutation in pediatric intracranial and cranial juvenile xanthogranuloma. Hum Pathol 2017, 69 : 118-122
128) Kong DS, Nam DH, Lee JI et al : Intracranial growing teratoma syndrome mimicking tumor relapse : a diagnostic dilemma. J Neurosurg Pediatr 2009, 3 : 392-396
129) Sekine S, Shibata T, Kokubu A et al : Craniopharyngiomas of adamantinomatous type harbor beta-catenin gene mutations. Am J Pathol 2002, 161 : 1997-2001
130) Larkin SJ, Preda V, Karavitaki N et al : BRAF V600E mutations are characteristic for papillary craniopharyngioma and may coexist with CTNNB1-mutated adamantinomatous craniopharyngioma. Acta Neuropathol 2014, 127 : 927-929
P.1752 掲載の参考文献
1) 小幡博人 : 眼球と付属器. 病理診断に直結した組織学. 病理と臨床 2017, 35 (臨時増刊号) : 87-96
2) 小幡博人 : 眼球. 病理解剖マニュアル. 病理と臨床 2012, 30 (臨時増刊号) : 77-80
3) 小幡博人 : 眼瞼腫瘍の診療の要点. 日眼会誌 2019, 123 : 785-804
4) Jakobiec FA, Mehta M, Iwamoto M et al : Intratarsal keratinous cysts of the meibomian gland : distinctive clinicopathologic and immunohistochemical features in 6 cases. Am J Ophthalmol 2010, 149 : 82-94
5) Jakobiec FA, Mendoza PR : Eyelid sebaceous carcinoma : clinicopathologic and multiparametric immunohistochemical analysis that includes addipophilin. Am J Ophthalmol 2014, 157 : 186-208
6) Jakobiec FA, Werdich X : Androgen receptor identification in the diagnosis of eyelid sebaceous carcinomas. Am J Ophthalmol 2014, 157 : 687-696
7) Shields CL, Shields JA : Tumors of the conjunctiva and cornea. Surv Ophthalmol 2004, 49 : 3-24
8) Shields CL, Chien JL, Surakiatchanukul T et al : Conjunctival tumors : review of clinical features, risks, biomarkers, and outcomes-The 2017 J. Donald M. Gass Lecture. Asia-Pac J Ophthalmol 2017, 6 : 109-120
9) 小幡博人 : 翼状片の病態と治療. 眼科 2005, 47 : 1917-1928
10) Mudhar HS : Melanocytic lesions of the conjunctiva. Diagnostic Histopathology 2014, 21 : 26-33
11) Obata H, Kubota M, Kawai T et al : Nevocellular nevus of the palpebral conjunctiva. Acta Ophthalmol Scand 2004, 82 : 632-633
12) Thotoka D, Morkin MI, Galor A et al : Update on diagnosis and management of conjunctival papilloma. Eye Vis (Lond) 2019, 6 : 18
13) Pizzarello LD, Jakobiec FA : Bowen's disease of the conjunctiva : a misnomer. In Jakobiec FA, eds., Ocular and adnexal tumours, Aesculapius, 1978, 553-571
14) Lee GA, Hirst LW : Ocular surface squamous neoplasia. Surv Ophthalmol 1995, 39 : 429-450
15) Verdijk RM : An update of ocular adnexal lymphomas. Diagnostic Histopathology 2015, 21 : 26-33
16) Obata H, Mori K, Tsuru T : Subconjunctival mucosa-associated lymphoid tissue (MALT) lymphoma arising in Tenon's capsule. Graefe's Arch Clin Exp Ophthalmol 2006, 244 : 118-121
17) 小幡博人 : 円錐角膜の病理. 眼科 2014, 56 : 1271-1276
18) 小幡博人 : 眼科医のための病理学. 54. 水疱性角膜症の病理. 眼科 2006, 48 : 519-524
19) Weiss JS, Moller HU, Aldave AJ et al : IC3D classification of corneal dystrophies-edition 2. Cornea 2015, 34 : 117-159
20) 小幡博人 : 眼科医のための病理学. 26. スリット所見と病理所見-顆粒状角膜ジストロフィと斑状角膜ジストロフィ. 眼科 2003, 45 : 1861-1864
21) 小幡博人 : 眼科医のための病理学. 53. 角膜にアミロイドが沈着する疾患. 眼科 2006, 48 : 255-259
22) 小幡博人 : 眼科医のための病理学. 27. 一枚の写真-2つの実質型角膜ヘルペス. 眼科 2003, 45 : 1995-1998
23) Eagle RC Jr : The pathology of ocular cancer. Eye 2013, 27 : 128-136
24) 禰津直也, 後藤浩, 馬詰和比古ほか : ぶどう膜悪性黒色腫の臨床的検討. 日眼会誌 2017, 121 : 413-418
25) McLean IW, Foster WD, Zimmerman LE et al : Modifications of Callender's Classification of Uveal Melanoma at the Armed Forces Institute of Pathology. Am J Ophthalmol 1983, 96 : 502-509
26) Eagle RC Jr : Uveal malignant melanoma. In ; Eye Pathology. An Atlas and Text, 3rd ed., Wolters Kluwer, 2017, 60-63
27) Grossniklaus HE, Eagle RC Jr, Albert D et al : Tumours of the iris, ciliary body, and choroid : In ; WHO Classification of Tumours of the Eye, 4th edition, WHO Press, 87-91, 2018
28) Font RL, Croxatto JO, Rao NA : Tumors of the uveal tract. In ; Tumors of the eye and ocular adnexa. AFIP atlas of tumor pathology, series 4, ARP Press, 41-84, 2006
29) 末岡健太郎, 嘉鳥信忠, 笠井健一郎 : 聖隷浜松病院眼形成眼窩外科における過去9年間の眼窩, 眼瞼, 結膜腫瘍の検討. 臨眼 2014, 68 : 463-470
30) Japanese study group of IgG4-related ophthalmic disease : A prevalence study of IgG4-related ophthalmic disease in Japan. Jpn J Ophthalmol 2013, 57 : 573-579
31) Goto H, Takahira M, Azumi A et al : Diagnostic criteria for IgG4-related ophthalmic disease. Jpn J Ophthalmol 2015, 59 : 1-7
32) Sogabe Y, Miyatani K, Goto R et al : Pathological findings of infraorbital nerve enlargement in IgG4-related ophthalmic disease. Jpn J Ophthalmol 2012, 56 : 511-514
33) Mulay K, Honavar SG : Idiopathic (non-specific) orbital inflammation. Diagnostic Histopathology 2015, 21 : 34-47

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