日本臨牀 別冊 血液症候群(第2版)II

出版社: 日本臨牀社
発行日: 2013-03-20
分野: 臨床医学:一般  >  雑誌
ISSN: 00471852
雑誌名:
特集: 血液症候群(第2版)II―その他の血液疾患を含めて―
電子書籍版: 2013-03-20 (第2版第1刷)
書籍・雑誌
≪全国送料無料でお届け≫
取寄せ目安:8~14営業日

17,160 円(税込)

電子書籍
章別単位で購入
ブラウザ、アプリ閲覧

17,160 円(税込)

目次

  • 日本臨牀 別冊 血液症候群(第2版)II

    ―目次―

    特集 血液症候群(第2版)II―その他の血液疾患を含めて―

    III. 白血球(顆粒球)の異常(悪性腫瘍を除く)    
     1 類白血病反応    
     2 好中球の異常    
     3 好酸球の異常    
     4 好塩基球の異常    
     5 単球の異常    
     6 肥満細胞の異常    

    IV. リンパ球の異常    
     1 リンパ球増加症    
     2 リンパ球減少症    
     3 伝染性単核症    
     4 リンパ球機能異常と類縁疾患    

    V. 血小板の異常    
     1 血小板増加症    
     2 血小板減少症    
     3 血小板機能異常症    

    VI. 血管障害による出血傾向    
     1 先天性血管性紫斑病    
     2 後天性血管性紫斑病    
     3 単純性紫斑病 
     4 老人性紫斑病 

    VII. 凝固・線溶異常による出血傾向    
     1 先天性凝固線溶異常症    
     2 後天性凝固線溶異常症    

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。

序文

P.10 掲載の参考文献
2) 宮地勇人 : 遺伝子関連検査のガイドライン. 日内会誌 100 : 3182-3192, 2011.
3) Swerdlow SH, et al (ed) : WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th ed, IARC Press, Lyon, 2008.
11) Pfreundschuh M, et al ; MabThera International Trial (MInT) Group : CHOP-like chemotherapy with or without rituximab in young patients with good-prognosis diffuse large-B-cell lymphoma : 6-year results of an open-label randomised study of the MabThera International Trial (MInT) Group. Lancet Oncol 12 : 1013-1022, 2011.

III 白血球 ( 顆粒球 ) の異常 ( 悪性腫瘍を除く )

P.17 掲載の参考文献
2) 中尾喜久, 三好和夫 : 類白血病性反応に就て-臨牀方面-. 日血会誌 14 (補冊) : 290-309, 1951.
3) Halkes CJ, et al : Extreme leucocytosis : not always leukaemia. Neth J Med 65 : 248-251, 2007.
4) 林泰秀 : 小児の治療指針類白血病反応. 小児科診療 58 : 374-377, 1995.
5) Nimieri HS, et al : Leukemoid reaction response to chemotherapy and radiotherapy in a patient with cervical carcinoma. Ann Hematol 82 : 316-317, 2003.
12) Azim T, et al : Lipopolysaccharide-specific antibodies in plasma and stools of children with Shigella-associated leukemoid reaction and hemolytic-uremic syndrome. Clin Diagn Lab Immunol 3 : 701-705, 1996.
P.21 掲載の参考文献
2) Swerdlow S, et al : WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th ed, IARC Press, Lyon, 2008.
13) Muramatsu H, et al : Low-dose cytosine arabinoside therapy for neonates with Down syndrome (DS) and transient leukemia (TL). ASH Annual Meeting Abstracts 116 : 1074, 2010.
14) 村松秀城, 菊地陽 : 一過性骨髄異常増殖症 (TAM) の治療戦略. 日小児血液会誌 25 : 179-184, 2011.
P.23 掲載の参考文献
P.25 掲載の参考文献
P.27 掲載の参考文献
P.29 掲載の参考文献
P.31 掲載の参考文献
P.34 掲載の参考文献
2) 佐藤勉ほか : Granulocyte colony stimulating factor (G-CSF) 産生腎癌. 臨床血液 38 : 1189-1192, 1997.
4) 畦西恭彦ほか : 好中球と好酸球の著しい増多を認めた結腸低分化腺癌の一例. 臨床血液 38 : 980, 1997.
7) Yuo A, et al : Recombinant human granulocyte colony-stimulating factor as an activator of human granulocytes : potentiation of responses triggered by receptor-mediated agonists and stimulation of C3bi receptor expression and adherence. Blood 74 : 2144-2149, 1989.
8) Kawakami M, et al : Levels of serum G-CSF in patients with infections. Blood 76 : 1962-1964, 1990.
P.37 掲載の参考文献
1) 谷憲三朗 : 好中球減少症. 三輪血液病学, 第3版 (浅野茂隆ほか編), p1293-1298, 文光堂, 2006.
2) 厚生労働省 : 重篤副作用疾患別対応マニュアル 無顆粒球症, p9-14, 2007.
3) Watanebe N, et al : Antithyroid drug-induced hematopoietic damage : a retrospective cohort study of agranulocytosis and pancytopenia involving 50,385 patients with Graves' disease. J Clin Endocrinol Metab 97 : E49-E53, 2012.
4) 田尻淳一ほか : 抗甲状腺剤による無顆粒球症 : 特に "Normal white blood cell count agranulocytosis" について. 日内分泌会誌 69 : 1013-1016, 1993.
5) Anderson F, et al : Systematic review : agranulocytosis induced by nonchemotherapy drugs. Ann Intern Med 146 : 657-665, 2007.
P.40 掲載の参考文献
4) Kohgo Y, et al : Chronic idiopathic neutropenia associated with abnormal expression of granulocyte colony-stimulating factor mRNA of bone marrow stromal cells. Int J Hematol 59 : 177-180, 1994.
6) Hirayama Y, et al : Concentrations of thrombopoietin in bone marrow in normal subjects and in patients with idiopathic thrombocytopenic purpura, aplastic anemia, and essential thrombocythemia correlate with its mRNA expression of bone marrow stromal cells. Blood 92 : 46-52, 1998.
7) Palmblad J, et al : Chronic mild neutropenia in adults-relation to IgG3 deficiency and infection susceptibility. Blood 96 : 31b, 2000.
8) Koene HR, et al : Clinical value of soluble IgG Fc receptor type II in plasma from patients with chronic idiopathic neutropenia. Blood 91 : 3962-3966, 1998.
P.45 掲載の参考文献
6) CEREDIH : The French PID study group : The French national registry of primary immunodeficiency diseases. Clin Immunol 135 (2) : 264-272, 2010.
P.49 掲載の参考文献
P.53 掲載の参考文献
6) 小林正夫 : 小児好中球減少症. 日児誌 109 : 614-622, 2005.
7) 中村和洋ほか : 抗好中球抗体と乳幼児自己免疫性好中球減少症. 日小児血液会誌 18 : 17-22, 2004.
11) 中村和洋, 小林正夫 : 新生児の好中球減少症. Jpn J Obstet Gynecol Neonatal Hematol 18 : 149-153, 2009.
P.56 掲載の参考文献
P.59 掲載の参考文献
3) 溝口洋子, 小林正夫 : 好中球減少症. 小児科 51 : 985-994, 2010.
6) Dale DC, et al : Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood 96 : 2317-2322, 2000.
7) Bellanne-Chantelot C, et al : Mutations in the ELA2 gene correlate with more severe expression of neutropenia : a study of 81 patients from the French Neutropenia Register. Blood 163 : 4119-4125, 2004.
P.63 掲載の参考文献
1) Shubitz KW : Qualitative disorders of leukocytes. In : Wintrobe's Clinical Hematology, 12th ed (ed by Greer JP, et al), p1548-1549, Lippincott Williams & Wilkins, Philadelphia, 2009.
2) Pelger K : Demonstratie van een paar zeldzaam voorkomende typen van bloedlichampjes en bespreking der patienten. Ned Tijdschr Geneesk 72 : 1178, 1928.
3) Huet GJ : Familial anomaly of leukocytes. Ned Tijdschr Geneesk 75 : 5956-5959, 1931.
9) Johnson CA, et al : Functional and metabolic studies of polymorphonuclear leukocytes in the congenital Pelger-Huetanomaly. Blood 55 : 466-469, 1980.
11) 栗山一孝 : 好中球の形態異常, 三輪血液病学, 第3版 (三輪史朗ほか編), p1287-1293, 文光堂, 2006.
12) Konttinen JM : Recurrent attacks of abdominal pain and fever with familial segmentation arrest of granulocytes. Blood 43 : 871-874, 1974.
15) Teshima T, et al : Effect of G-CSF, GM-CSF, and IL-5 on nuclear segmentation of neutrophils and eosinophils in congenital or acquired Pelger-Huet anomaly. Exp Hematol 19 : 322-325, 1991.
P.67 掲載の参考文献
1) Shubitz KW : Qualitative disorders of leukocytes. In : Wintrobe's Clinical Hematology (ed by Greer JP, et al), 12th ed, p1548-1550, Lippincott Williams & Wilkins, Philadelphia, 2009.
2) May R : Leukozyteneinschlusse. Dtsch Arch Klin Med 96 : 1-6, 1909.
3) Hegglin R : Simultaneous constitutional changes in neutrophils and platelets. Helv Med Acta 12 : 439-440, 1945.
15) Gropper S, et al : A patient with Fechtner syndrome successfully treated with romiplostim. Thromb Haemost 107 : 590-591, 2012.
P.69 掲載の参考文献
1) Alder A : Uber konstitutionell bedingte Granultions-vernderungen der Leukozyten. Dtsch Arch Klin Med 183 : 372-378, 1939.
3) Athens JW : Qualitative disorders of leukocytes. In : Wintrobe's Clinical Hematology, 12th ed (ed by Greer JP, et al), p1548-1549, Lippincott Williams & Wilkins, Philadelphia, 2009.
4) 栗山一孝 : 好中球の形態異常. 血液学, 第3版 (三輪史朗ほか編), p1287-1293, 文光堂, 2006.
13) Grgic Z, Kalafatic Z : Three cases of in complete Alder's granulation anomaly. Schweiz Med Wochenschr 88 : 994-995, 1958.
16) Gitzelmann R, et al : Unusually mild course of β-glucuronidase deficiency in two brothers (mucopolysaccharidosis VII). Helv Paediatr Acta 33 : 413-428, 1978.
P.73 掲載の参考文献
2) 東音高 : Chediak-Higashi症候群. 日本臨牀 35 (増刊号 : 症候群 1977) : 928-929, 1977.
3) Shubitz K M : Qualitative disorders of leukocytes. In : Wintrobe's Clinical Hematology, 12th ed (ed by Greer JP, et al), p1550-1552, Lippincott Williams & Wilkins, Philadelphia, 2009.
4) 安井耕三 : 先天性遺伝性食細胞機能異常症のmolecular basisについての最近の知見 Chediak-Higashi症候群の遺伝子異常を中心として. 日臨免疫会誌 20 : 145-151, 1997.
8) 石井榮一ほか : 分泌顆粒の異常と血液疾患. 臨床血液 49 : 225-233, 2008.
9) 宇山栄一郎ほか : Chediak-Higashi症候群成人例の神経学的検討 parkinsonismと著明な脳脊髄萎縮に注目して. 臨床神経学 31 : 24-31, 1991.
11) 湯尾明 : 機能異常 好中球の異常. 三輪血液病学, 第3版, p1305-1308, 文光堂, 2006.
12) 鈴木信寛 : 血球貪食症候群. 臨床血液 49 : 159-168, 2008.
15) Haddad BE, et al : Treatment of Chediak-Higashi syndrome by allogenic bone marrow transplantation : report of 10 cases. Blood 85 : 3328-3333, 1995.
P.77 掲載の参考文献
6) Skubitz KM : Qualitative disorders of leukocytes. In : Wintrobe's Clinical Hematology, 10th ed, Vol 2 (ed by Lee GR, et al), p1899-1900, Williams & Wilkins, Philadelphia, 1999.
9) Morishita K, et al : Chromosomal gene structure of human myeloperoxidase and regulation of its expression by granulocyte colony-stimulating factor. J Biol Chem 262 : 15208-15213, 1987.
14) Ishida-Okawara A, et al : Contribution of myeloperoxidase to coronary artery vasculitis associated with MPO-ANCA production. Inflammation 25 : 381-387, 2001.
15) Fujii A, et al : Epitope analysis of myeloperoxidase (MPO) specific anti-neutrophile cytoplasmic autoantibodies (ANCA) in MPO-ANCA-associated glomerulonephritis. Clin Nephrol 53 : 242-252, 2000.
P.80 掲載の参考文献
P.84 掲載の参考文献
1) Borregaard N, et al : Granules of the human neutrophilic polymorphonuclear leukocytes. Blood 89 : 3503-3521, 1997.
2) 小宮山淳 : 好中球特殊顆粒欠損症. 好中球機能低下と機能亢進 (笹田昌孝編), p145-157, 医薬ジャーナル社, 1998.
5) Tamura A, et al : A marked decrease in defensin mRNA in the only case of congenital neutrophil specific granule deficiency reported in Japan. Int J Hematol 59 : 137-142, 1994.
6) Lekstrom-Himes J, et al : Neutrophil-specific granule deficiency results from a novel mutation with loss of function of the transcription factor CCAAT/enhancer binding protein ε. J Exp Med 189 : 1847-1852, 1999.
P.87 掲載の参考文献
2) Nunoi H, et al : A heterozygous mutation of beta-actin associated with neutrophil dysfunction and recurrent infection. Proc Natl Acad Sci USA 96 : 8693-8698, 1999.
3) Coates TD, et al : An inherited defect of neutrophil motility and microfilamentous cytoskeleton associated with abnormalities in 47-Kd and 89-Kd proteins. Blood 78 : 1338-1346, 1991.
6) Roos D, et al : A novel syndrome of severe neutrophil dysfunction : unresponsiveness confined to chemotaxin-induced functions. Blood 81 : 2735-2743, 1993.
8) 岡村精一, 仁保喜之 : 好中球アクチン機能異常症. 別冊日本臨牀 血液症候群 (II), p73-75, 日本臨牀社, 1998.
12) Howard T, et al : The 47-kD protein in creased in neutrophil actin dysfunction with 47- and 89-kD protein abnormalities is lymphocyte-specific protein. Blood 83 : 231-241, 1994.
13) Packman CH, Lichtman MA : Activation of neutrophils : measurement of actin conformational changes by flow cytometry. Blood Cells 16 : 193-207, 1990.
P.92 掲載の参考文献
1) Davis SD, et al : Job's Syndrome. Recurrent, "cold", staphylococcal abscesses. Lancet 1 : 1013-1015, 1966.
2) Buckley RH, et al : Extreme hyperimmunoglobulinemia E and undue susceptibility to infection. Pediatrics 49 : 59-70, 1972.
9) Milner JD, et al : Impaired TH17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome. Nature 452 : 773-776, 2008.
P.94 掲載の参考文献
P.98 掲載の参考文献
4) Lekstrom-Himes JA, et al : Inhibition of human neutrophil IL-8 production by hydrogen peroxide and dysregulation in chronic granulomatous disease. J Immunol 174 : 411-417, 2005.
10) Winkelstein JA, et al : Chronic granulomatous disease. Report on an national registry of 368 patients. Medicine (Baltimore) 79 : 155-169, 2000.
12) 水上智之 : 慢性肉芽腫症. 臨床検査 53 : 593-597, 2009.
P.100 掲載の参考文献
P.103 掲載の参考文献
6) Hasebe M : A case of Jordans' anomaly. Rinsho Ketsueki 24 (5) : 553-558, 1983.
P.108 掲載の参考文献
1) 小宮山淳 (編) : 好中球機能異常症. 小児の血液疾患, p86-102, 永井書店, 1994.
6) Walr and S, et al : In vivo evidences that insulin regulates human polymorphonuclear neutrophil functions. J Leuk Biol 76 : 1104-1110, 2004.
10) Haag-Weber M, Horl WH : Dysfunction of polymorphonuclear leukocytes in uremia. Semin Nephrol 16 : 192-201, 1996.
P.111 掲載の参考文献
2) Kiersztejn M, et al : On the mechanisms of impaired phagocytosis in phosphate depletion. J Am Soc Nephrol 2 : 1484-1489, 1992.
4) Theander S, et al : Granule-specific ATP requirements for Ca2+-induced exocytosis in human neutrophils. Evidence for substantial ATP-independent release. J Cell Sci 115 : 2975-2983, 2002.
P.113 掲載の参考文献
2) 朝長万左男 : 好中球の Pelger-Huet核異常をめぐって. 臨床病理 53 : 54-60, 2005.
4) 不応性貧血 (骨髄異形成症候群) の形態学的診断基準作成のためのワーキンググループ. 朝長万左男, 松田晃 (編) : 不応性貧血 (骨髄異形成症候群) の形態学的異形成に基づく診断確度区分と形態診断アトラス. 厚生労働科学研究費補助金難治性疾患克服研究事業特発性造血障害に関する調査研究 (平成19年度) (主任研究者小澤敬也), 2008.
P.115 掲載の参考文献
P.118 掲載の参考文献
1) Loffler W : Zur Differential-Diagnose der Lungeninfiltrierungen, II. Uber Fluchtige Succedan-Infiltrate (mit Eosinophilie). Beitr Klin Tuberk 79 : 368-392, 1932.
2) Loffler W : Transient lung infiltrations with blood eosinophilia. Int Arch Allergy Appl Immunol 8 : 54-59, 1956.
3) 矢野平一, 片山俊夫 : 白血球 (顆粒球) の異常 : PIE症候群 : Loffler症候群. 別冊日本臨牀 血液症候群 (II), p98-100, 日本臨牀社, 1998.
4) Reeder WH, Goodrich BE : Pulmonary infiltration with eosinophilia (PIE syndrome). Ann Intern Med 36 : 1217-1240, 1952.
9) Fraser RS, et al : Eosinophilic lung disease. In : Synopsis of Diseases of the Chest, 3rd ed, p511-514, Elsevier, New York, 2005.
10) Weller PF, Bubley GJ : The idiopathic hypereosinophilic syndrome. Blood 83 : 2759-2779, 1994.
12) Te Booij M, et al : Loffler syndrome caused by extensive cutaneous larva migrans : a case report and review of the literature. Dermatol Online J 16 (10) : 2, 2010.
15) Lazoglu AH, et al : Phenytoin-related immunodeficiency associated with Loeffler's syndrome. Ann Allergy Asthma Immunol 74 : 479-482, 1995
P.122 掲載の参考文献
7) Fraser RS, et al : Eosinophilic lung disease. In : Synopsis of Diseases of the Chest, 3rd ed, p511-514, Elsevier. New York, 2005.
8) Turner-Warwick M, et al : Cryptogenic pulmonary eosinophilia. Clin Allergy 6 : 135-145, 1976.
14) Webb WR, et al : Hypersensitivity pneumonitis and eosinophilic lung diseases. In : High-Resolution of the Lung, 4th ed, p335-355, Lippincott Williams & Wilkins, Philadelphia, 2009.
P.125 掲載の参考文献
2) Reeder WH,Goodrich BE : Pulmonary infiltration with eosinophilia (PI E syndrome). Ann Intern Med 36 : 1217-1240, 1952.
3) 吉澤靖之ほか : アレルギー性気道・肺疾患. EBM現代内科学 (黒川清ほか編), p352-357, 金芳堂, 1997.
4) 近藤有好 : 好酸球性肺炎. 呼吸器疾患 (原沢道美, 北村諭編), p358-362, 医歯薬出版, 1994.
6) Webb WR, et al : Airways diseases. In : High-Resolution of the Lung, 4th ed, p492-554, Lippincott Williams & Wilkins, Philadelphia, 2009.
P.132 掲載の参考文献
1) Churg J, Strauss L : Allergic granulomatosis, allergic angiitis and periarteritis nodosa. Am J Pathol 27 : 277-301, 1951.
3) Jennette JC, et al : Nomenclature of systemic vasculitides. Proposal of an international consensus conference. Arthritis Rheum 37 : 187-192, 1994.
5) Ramentol-Sintas M, et al : Churg-Strauss Syndrome : An evolving paradigm. Autoimmun Rev, 2012. [Epub ahead of print]
7) Matsumoto Y, et al : Nationwide epidemiological survey of refractory vasculitis (anti-neutrophil cytoplasmic antibody (ANCA) -associated vasculitis, anti-phospholipid syndrome and temporal arteritis) in Japan. Annual Report of the Research Committee on Intractable Vasculitides, the Ministry of Health and Welfare of Japan [in Japanese], p15-23, 1998.
8) Amano K, et al : Studies on allergic granulomatous angiitis (Churg Strauss syndrome) in Japan : nationwide epidemiological survey. Annual Report of the Research Committee on Intractable Vasculitides, the Ministry of Health and Welfareof Japan [in Japanese], p98-99, 2010.
14) Sable-Fourtassou R, et al : Antineutrophil cytoplasmic antibodies and the Churg-Strauss syndrome. Ann Intern Med 143 : 632-638, 2005.
P.138 掲載の参考文献
1) Wegener F : Uber eine einartige rhino-gene Granulomatose mit besonderer Beteligungdes arteriensystems und der Nieren. Beitr Pathol 102 : 36-38, 1939.
2) Falk RJ, et al : Granulomatosis with polyangiitis (Wegener's) : an alternative name for Wegener's granulomatosis. Arthritis Rheum 63 : 863-864, 2011.
4) 吉田雅治, 長澤俊彦 : Wegener肉芽腫症における抗好中球細胞質抗体の意義. 医学のあゆみ 145 : 649-650, 1988.
6) De Remee RA, et al : Wegener's granulomatosis. Anatomic correlates. A proposal classification. Mayo Clin Proc 51 : 777-781, 1975.
7) 吉田雅治 : Wegener肉芽腫症. 腎と透析 68 : 59-66, 2010.
8) Yoshida M, et al : Two types of myeloperoxidase-antineutrophil cytoplasmic autoantibodies with high affinity and a low affinity in small vessel vasculitis. Clin Exp Rheumatol 27 (Suppl 52) : S28-32, 2009.
13) 吉田雅治 : 腎炎, ネフローゼ症候群に対する免疫抑制療法の進歩. 日腎会誌 52 : 1, 2010.
14) Stegemen CA, et al : Trimethoprim-sulfamethoxazale (co-trimoxazole) for the prevention of relapse of Wegener's granulomatosis. N Engl J Med 335 : 16-20, 1996.
15) Yoshida M, et al : Rapid decrease of anti-β-glucan antibody as an indicator for early diagnosis of carinii pneumonitis and deep mycotic infections following immunosuppressive therapy in antineutrophil cytoplasmic antibody-associated vasculitis. Clin Rheumatol 28 : 565-571, 2009.
P.143 掲載の参考文献
2) Jennette JC, et al : Nomenclature of systemic vasculitides. Proposal of an international consensus conference. Arthritis Rheum 37 : 187-192, 1994.
3) de Menthon M, Mahr A : Treating polyarteritis nodosa : current state of the art. Clin Exp Rheumatol 29 (Suppl 64) : S110-116, 2011.
4) 中林公正ほか : 結節性多発動脈炎. 血管炎アトラス (尾崎承一, 吉木敬編), p9-12, 厚生労働省難治性疾患克服研究事業難治性血管炎に対する調査研究班, 2005.
5) 難治性血管炎調査研究班 : 結節性動脈周囲炎. 難病の診断と治療指針 1 (難病医学研究財団企画委員会編), p107-115, 六法出版, 1997.
6) 吉田雅治ほか : 中・小型血管炎の臨床に関する小委員会報告. 厚生省特定疾患免疫疾患調査研究班, 難治性血管炎分科会, 平成10年度研究報告書, p239-243, 1999.
P.147 掲載の参考文献
7) 定明子, 松井利充 : 本邦における慢性好酸球性白血病/特発性好酸球増多症候群の臨床像と治療. 臨床血液 51 : 515-525, 2010.
8) Bain BJ, et al : Chronic eosinophilic leukaemia, not otherwise specified. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, International Agency for Research on Cancer, p51-53, IARC Press, Lyon, 2008.
10) 江副幸子 : 好酸球増多症の病因・病態と治療. 別冊日本臨牀 造血器腫瘍学, p330-336, 日本臨牀社, 2012.
13) 小池道明, 友安茂 : 特発性好酸球増加症候群. 別冊日本臨牀 血液症候群 II, p119-122, 日本臨牀社, 1998.
14) Baccarani M, et al : The efficacy of imatinib mesylate in patients with FIP1L1-PDGFR α-positive hypereosinophilic syndrome. Results of amulticenter prospective study. Haematologica 92 : 1173-1179, 2007.
P.151 掲載の参考文献
1) Engfeldt B, Zetterstrom R : Disseminated eosinophilic collagen disease ; a clinical and pathological study of a clinical entity related to Loffler's syndromes. Acta Med Scand 153 : 337-353, 1956.
2) Bousser J : Eosinophilie et leucemie. Sang 28 : 553-580, 1957.
7) World Health Organization Classification of Tumours : Pathology and Genetics of Tumors of Haematopoietic and Lymphoid Tissues (ed by Jaffe ES, et al), IARC Press, Lyon, 2001.
8) WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues (ed by Swerdlow SH, et al), IARC Press, Lyon, 2008.
10) 柴田昭 : 播種性好酸球性膠原病. 診断と治療 2 : 299-305, 1980.
11) 南陸彦 : Disseminated Eosinophilic Collagen Disease. 小児科診療 41 : 673-676, 1978.
12) 津田俊彦ほか : 播種性好酸性膠原病の1例. 臨血 16 : 1124-1130, 1975.
13) 更井哲夫ほか : 播種性好酸性膠原病の1例. 臨血 17 : 1198-1206, 1976.
14) 大沢修子, 長沼雄峰 : Disseminated eosinophilic collagen diseaseと思われる1症例. 小児科臨床 36 : 63-68, 1983.
15) 定明子, 松井利充 : 本邦における慢性好酸球性白血病/特発性好酸球増多症候群の臨床像と治療. 臨血 21 : 515-525, 2010.
P.154 掲載の参考文献
2) 端本宇志ほか : 無治療で自然経過を観察したnon-episodic angioedema with eosinophilia. 日皮会誌 118 : 925-931, 2008.
5) Butterfield JH, et al : Elevated serum levels of interleukin-5 in patients with the syndrome of episodic angioedema and eosinophilia. Blood 79 (3) : 688-692, 1992.
7) Ackerman SJ, Butterfield JH : Eosinophilia, eosinophil-associated diseases, chronic eosinophilic leukemia, and the hypereosinophilic syndrome. In : Hematology : Basic Principles and Practice (ed by Hoffman R, et al), 4th ed, p763-786, Elsevier, Philadelphia, 2005.
8) 川口康久ほか : 繰り返した好酸球性血管性浮腫. 臨床血液 44 : 1020-1025, 2003.
P.158 掲載の参考文献
5) 木下芳一ほか : 好酸球性胃腸炎の診断と治療. 日消誌 56 (6) : 1797-1805, 2012.
P.163 掲載の参考文献
1) 岡村精一 : 好酸球増加のプライマリケア. 治療 84 (2) : 236-239, 2002.
2) 丸山治彦 : 寄生虫疾患と好酸球・好塩基球. 臨床検査 51 (10) : 1047-1052, 2007.
3) 有薗直樹 : 国内の寄生虫症の動向. 治療学 37 (6) : 567-570, 2003.
4) Nakamura-Uchiyama F, et al : The Current Statusof Parasitic Disease in Japan. Intern Med 42 (3) : 222-236, 2003.
5) 有薗直樹 : 日本における蠕虫症と蠕虫研究の近年の動向. Clinical Parasitology 22 (1) : 9-17, 2011.
9) Chihara J, et al : IL-5 and IL-5 receptor expression on human eosinophils in relation to eosinophil activation. Biotechnol Ther 4 (3 & 4) : 271-283, 1993.
11) Torisu M, et al : Eosinophilic granuloma formation in Anisakiasis. Basic mechanisms of granulomatous inflammation : proceedings of the International Symposium on Basic Mechanisms of Granulomatous Inflammation, held in Fukuoka, Japan, 28-29 November 1988. p207-219, Excerpta Medica. Amsterdam, 1989.
12) 吉村堅太郎 : 寄生虫症における好酸球の寄生虫殺滅作用の機序. 日本臨牀 51 (3) : 657-663, 1993.
15) 佐藤直樹ほか : 多包性肝エキノコックス症に対するbenzimidazole系薬剤の効果. 日消誌 91 (7) : 1197-1204, 1994.
P.167 掲載の参考文献
1) 金井泉, 金井正光 : 末梢血白血球分類の診断的意義. 臨床検査法提要, 第31版, p306-309, 金原出版, 1998.
2) 松村到, 金倉譲 : 好塩基球の増加する疾患, 減少する疾患. 三輪血液病学, 第3版 (浅野茂隆ほか監), p1314-1320, 文光堂, 2006.
3) Parker RI, Metcalfe DD : Basophils, mast cells, and systemic mastocytosis. In : Hematology-Basic Principles and Practice- (ed by Hoffman R, et al), p911-925, Elsevier, Philadelphia, 2005.
4) Chang KL, Forman SJ : Myeloid disorders. In : Atlas of Clinical Hematology (ed by Armitage JO), p149, Lippincott Williams & Wilkins, Philadelphia, 2004.
5) Befus AD, Denbrug JA : Chapter 11, Basophilic lymphocytes : mast cells and basophils. In : Wintrobe's Clinical Hematology (ed by Greer JP, et al), p236-248, Lippincott Williams & Wilkins, Philadelphia, 2009.
9) Chi Y, et al : Acute myelogenous leukemia with t (6 ; 9) (p23 ; q34) and marrow basophilia : an overview. Arch Pathol Lab Med 2132 : 1835-1857, 2008.
10) Staal-Viliare A, et al : A case of de novo acute basophilic leukaemia : diagnostic criteria and review of the literature. Ann Biol Clin (Paris) 64 : 361-365, 2006.
P.169 掲載の参考文献
1) 金井泉, 金井正光 : 末梢血白血球分類の診断的意義. 臨床検査法提要, 第31版, p306-309, 金原出版, 1998.
2) 松村到, 金倉譲 : 好塩基球の増加する疾患, 減少する疾患. 三輪血液病学, p1314-1320, 文光堂, 2006.
3) Parker RI, Metcalfe DD : Basophils, mast cells, and systemic mastocytosis. In : Hematology-Basic Principles and Practice- (ed by Hoffman R, et al), p911-925, Elsevier, Philadelphia, 2005.
4) Befus AD, Denbrug JA : Chapter 11, Basophilic lymphocytes : mast cells and basophils. In : Wintrobe's Clinical Hematology (ed by Greer JP, et al), p236-248, Lippincott Williams & Wilkins, Philadelphia, 2009.
P.172 掲載の参考文献
1) 木村文彦 : M-CSF. サイトカインのすべて. 臨床免疫・アレルギー科 57 (Suppl 21) : 588-593, 2012.
2) Lichtman MA : Monocytosis and monocytopenia. In : Williams Hematology (ed by Kaushansky K, et al), 8th ed, p1041-1046, McGraw Hill, New York, 2010.
8) Weiner LM, et al : Phase I trial of recombinant macrophage colony-stimulating factor and recombinant gamma-interferon : toxicity, monocytosis, and clinical effects. Cancer Res 54 : 4084-4090, 1994.
P.176 掲載の参考文献
2) 元吉和夫 : 単球・マクロファージ. 血液病学 (三輪史朗編), p303-313, 文光堂, 2006.
3) 木村文彦 : 造血因子 M-CSF. 臨床免疫・アレルギー内科 57 (Suppl 21) : 588-593, 2012.
5) 川越富夫ほか : 末梢血白血球数が12万/μlにまで上昇し, 慢性骨髄単球性白血病が疑われた類白血病反応の1例. 内科 106 : 757-760, 2010.
6) 元吉和夫 : 単球, マクロファージの疾患. 血液病学 (三輪史朗編), p1321-1322, 文光堂, 2006.
7) Janowska-Wieczorek A, et al : Increased circulating colony-stimulating factor-1 in patients with preleukemia, leukemia, and lymphoid malignancies. Blood 77 : 1796-1803, 1991.
8) 吉田勝彦ほか : 単球増加を認めた形質細胞白血病. 臨床血液 38 : 604-609, 1997.
9) 元吉和夫 : 単球性類白血病反応. 別冊日本臨牀 血液症候群 II, p146-148, 日本臨牀社, 1998.
11) 原田浩徳 : MDS分子病態. 臨床血液 52 : 113-122, 2011.
13) Melo JV, et al : P190 BCR-ABL chronic myeloid leukaemia : the missing link with chronic myelomonocytic leukaemia? Leukemia 8 : 208-211, 1994.
P.180 掲載の参考文献
P.184 掲載の参考文献

IV リンパ球の異常

P.190 掲載の参考文献
1) Penn I, et al : Malignant lymphomas in transplantation patients. Transplant Proc 1 : 106-112, 1969.
9) Swerdlow SH, et al : Post-transplant lymphoproliferative disorder. In : WHO classification of tumours of haematopoietic and lymphoid tissues, edn4 (ed by Swerdlow SH, et al), p343-349, Internal agency for research on cancer, Lyon, France, 2008.
13) Benkerrou M, et al : Anti-B-cell monoclonal antibody treatment of severe posttransplant B-lymphoproliferative disorder : prognostic factors and long-term outcome. Blood 92 : 3137-3147, 1998.
P.195 掲載の参考文献
1) Chan WC, et al : T-cell large granular lymphocytic leukaemia. In : WHO classification of tumours of haematopoietic and lymphoid tissues, 4th ed (ed by Swerdlow SH, et al), p272-273, Internal agency for research on cancer, Lyon, France, 2008.
P.199 掲載の参考文献
5) Sumegi J, et al : Correlation of mutations of the SH2D1A gene and Epstein-Barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease. Blood 96 : 3118-3125, 2000.
17) Lankster AC, et al : Allogeneic stem cell transplantation in X-linked lymphoproliferative disease : two cases in one family and review of the literature. Bone Marrow Transplant 36 : 99-105, 2005.
P.203 掲載の参考文献
1) 秋山暢 : 白血球増加と類白血病反応. 血液の事典 (平井久丸ほか編), p141-143, 朝倉書店, 2004.
4) 青木定夫 : 白血球数の増加. medicina 45 : 2202-2205, 2008.
6) 近藤誠司ほか : 関節リウマチ患者に生じた形質細胞による一過性の類白血病反応. 臨床血液 48 : 632-636, 2007.
7) Hutchinson RE, et al : Lymphocytic surface markers in lymphoid leukemoid reaction. Clin Lab Med 8 : 237-245, 1988.
P.207 掲載の参考文献
1) 岩田力 : 原発性免疫不全症の分類と我が国におけるその頻度. 小児科 47 : 3-16, 2006.
3) Miale J B : Laboratory Medicine Hematology, 4th ed, p900, C. V. Mosby, 1972.
4) 標準血液病学 (池田康夫, 押味和夫編), p285, 医学書院, 2000.
P.210 掲載の参考文献
2) Miale JB : Laboratory Medicine Hematology, 4th ed, p900, C. V. Mosby, St. Louis, 1972.
3) 標準血液病学 (池田康夫, 押味和夫編), p285, 医学書院, 2000.
P.214 掲載の参考文献
2) Centersfor Disease Control (CDC) : Unexplained CD4+ T-lymphocyte depletion in persons without evident HIV infection-United States. MMWR Morb Mortal Wkly Rep 41 : 541-545, 1992.
3) De Hovitz JA, et al : Idiopathic CD4+ T-lymphocytopenia. N Engl J Med 329 : 1045-1046, 1993.
17) Petersen EJ, et al : Allogeneic bone marrow transplantation can restore CD4+ T-lymphocyte count and immune function in idiopathic CD4+ T-lymphocytopenia. Bone Marrow Transplant 18 : 813-815, 1996.
P.218 掲載の参考文献
P.222 掲載の参考文献
P.226 掲載の参考文献
P.230 掲載の参考文献
1) Bruton OC : Agammaglobulinemia. Pediatrics 9 : 722-728, 1952.
3) Vitrie D, et al : The gene involved in X-linked agammaglobulinemia is a member of the src family of protein-tyrosine kinases. Nature 361 : 226-234, 1993.
7) 峯岸克行 : BTK欠損を伴わない無ガンマグロブリン血症. 小児内科 40 (増刊号) : 1271-1274, 2008.
13) Futatani T, et al : Deficient expression of Bruton's tyrosine kinase in monocytes from X-linked agammaglobulinemia as evaluated by a flow cytometric analysis and its clinical application to carrier detection. Blood 91 : 595-602, 1998.
P.236 掲載の参考文献
1) 森尾友宏 : 分類不能型免疫不全症. 日本臨牀 70 (11) : 2011-2021, 2012.
2) 森尾友宏 : 分類不能型免疫不全症 Update. 日臨免疫会誌 35 : 14-22, 2012.
11) Kamae C, et al : Classification of common variable immunodeficiency by quantification of T cell receptor and Ig kappa-deleting recombination circles. J Allerg Clin Immunol. (inpress)
P.241 掲載の参考文献
4) CEREDIH TFPSG : The French national registry of primary immunodeficiency diseases. Clin Immunol 135 (2) : 264-272, 2010.
6) Levy J, et al : Clinical spectrum of X-linked hyper-IgM syndrome. J Pediatr 131 (1 Pt 1) : 47-54, 1997.
14) Aghamohammadi A, et al : Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome. J Investig Allergol Clin Immunol 20 (5) : 442-445, 2010.
P.244 掲載の参考文献
1) Conley ME, et al : Diagnostic criteria forprimary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies). Clin Immunol 93 : 190-197, 1999.
2) Geha RS, et al : Primary immunodeficiency diseases : an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee. J Allergy Clin Immunol 120 : 776-794, 2007.
6) Cunningham-Rundles C : Physiology of IgA and IgA deficiency. J Clin Immunol 21 : 303-309, 2001.
P.248 掲載の参考文献
1) Kouvalainen K, et al : Chronic moniliasis, pyodermia and impaired capacity to form gamma-M antibodies. Ann Paediatr Fenn 12 : 256-262, 1966.
13) 鳥羽剛ほか : 健康小児の血清免疫グロブリン (IgG, IgA, IgM) 年齢別正常値および正常範囲に関する一考察. アレルギー 21 : 608-613, 1972.
P.252 掲載の参考文献
1) Conley ME, et al : Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies). Clin Immunol 93 : 190-197, 1999.
4) Stiehm ER, et al : IgG subclass deficiency. In : Immunological Disorders in Infants & Children (ed by Stiehm ER, et al), p393-398, Elsevier Saunders, Philadelphia, 2004.
6) Zhao Y, et al : Selective IgG2 deficiency due to a point mutation causing abnormal splicing of the Cgamma 2 gene. Int Immunol 17 : 95-101, 2005.
7) Terada T, et al : Analysis of Ig subclass deficiency : First reported caseof IgG2, IgG4, and IgA deficiency caused by deletion of C alpha 1, psi C gamma, Cgamma 2, Cgamma 4, and C epsilon in a Mongoloid patient. J Allergy Clin Immunol 108 : 602-606, 2001.
10) Oxelius VA, et al : IgG3 deficiency : common in obstructive lung disease. Hereditary in families with immunodeficiency and autoimmune disease. Monogr Allergy 20 : 106-115, 1986.
12) Soderstrom T, et al : Immunoglobulin subclasses and prophylactic use of immunoglobulin in immunoglobulin G subclass deficiency. Cancer 68 : 1426-1429, 1991.
P.256 掲載の参考文献
2) 奥田邦雄ほか : トランスコバラミンII欠乏症 血液と脈管シリーズ 4. ビタミン B12-基礎と臨床-, p179-186, 科学評論社, 1978.
3) Colob-Otero G, et al : Disorder of cobalamin and folate metabolism. In : Fundamental of Clinical Hematology (ed by Thorup O), p185-211, WB Saunders Company, Philadelphia-London-Toronto-Sydney-Tokyo-Hong Kong, 1987.
4) Rogec A, et al : The cloning and characterization of the human transcobalamin II gene. Blood 85 : 2711-2719, 1995.
6) Haberle J, et al : TC II deficiency : avoidance of false-negative molecular genetics by RNA-based investigation. J Hum Genet 54 : 331-334, 2009.
7) Qian L, et al : Congenital transcobalamin II deficiency due to errors in RNA editing. Blood cells Mol Dis 28 : 134-142, disucussion 143-145, 2002.
8) Manuel S, et al : Should transcobalain deficiency be treated aggressively? J Inherit Metab Dis 33 : 223-229, 2010.
9) 渡辺文雄ほか : ビタミン B12. 日本臨牀 57 : 2205-2210, 2000.
13) Gottleb C, et al : Rapid charcoal assay for intrinsic factor (IF), gastric juice unsaturated B12 binding capacity. Blood 25 : 875-884, 1965.
14) 内山幸信 : トランスコバラミン欠乏症. Jpn J Electroph 38 (6) : 403-410, 1994.
15) 内山幸信 : ビタミンの臨床. Modern Physician 27 (9) : 1216-1219, 2007.
P.260 掲載の参考文献
1) Di George AM : Discussion on a new concept of the cellular basis of immunity. J Pediatr 67 : 907, 1965 (abstract).
2) 岩田力 : 胸腺の発生障害と免疫不全症. 免疫・ Immunology Frontier 11 : 43-45, 2001.
5) McDonald-McGinn DM, et al : 22q11.2 Deletion Syndrome. In : Gene Reviews TM (ed by Pagon RA, et al) [internet], University of Washington, Seattle, 1993-.
9) Yamagashi H, Srivastava D : Unravelling the genetic and developmental mysteries of 22q11 deletion syndrome. Trends Mol Med 9 : 383-389, 2003.
12) Hisato Y, et al : Role of TBX1 in human del22q11.2 syndrome. Lancet 362 : 1366-1373, 2003.
P.264 掲載の参考文献
2) Hirshhorn R, Canotti F : Immunodeficiency due to defects of purine metabolism. In : Primary Immunodeficiency Diseases : A Molecular and Genetic Approach, 2nd ed (ed by Ochs HD, et al), p169-196, Oxford University Press, Inc, New York, 2007.
3) Hershfield MS, Mitchell BS : Immunodeficiency diseases caused by adenosine deaminase deficiency and purine nucleoside phosphorylase deficiency. In : The Metabolic and Molecular Basis of Inherited Disease, 8th ed (ed by Scriver CR, et al), p2585-2625, McGraw-Hill, New York, 2001.
4) Knutsen AP : Purine Nucleoside Phosphorylase Deficiency. In : Medscape Reference [Internet] (ed by Jyonouchi H, et al), Updated Aug 29, 2011.
5) Markert ML : Purine nucleoside phosphorylase deficiency. Immunodefic Rev 3 : 45-81, 1991.
6) 吉田泰祥ほか : Purine nucleoside phosphorylase欠損症の一例. 日児誌 90 : 2497-2502, 1986.
7) 崎山武志 : プリンヌクレオシドホスホリラーゼ (PNP). 日本臨牀 54 : 3220-3225, 1996.
8) Arpaia E, et al : Mitochondrial basis for immune deficiency. Evidence from purine nucleoside phosphorylase-deficient mice. J Exp Med 191 : 2197-2208, 2000.
13) Al-Saud B, et al : A novel mutation in purine nucleoside phosphorylase in a child with normal uric acid levels. Clin Biochem 42 : 1425-1727, 2009.
P.268 掲載の参考文献
1) Wolf B : Disorders of biotin metabolism. In : The metabolic and molecular bases of inherited disease (ed by Scriver CR, et al), p3151-3177, McGraw-Hill, NY, 1995.
5) Wolf B, Feldman GL : The biotin-dependent carboxylase deficiencies. Am J Hum Genet 34 : 699-716, 1982.
P.276 掲載の参考文献
P.280 掲載の参考文献
P.283 掲載の参考文献
2) Alonso K, et al : Thymic alymphoplasia and congenital aleukocytosis (reticular dysgenesia). Arch Pathol 94 : 179-183, 1972.
5) Reticular dysgenesis : http://www.orpha.net/
8) Kohler C, et al : Release of adenylate kinase 2 from the mitochondrial intermemberane space during apoptosis. FEBS Lett 447 : 10-12, 1999.
12) Bujan W, et al : Effect of recombinant human granulocyte colony-stimulating factor in reticular dysgenesis. Blood 82 : 1684, 1993.
P.287 掲載の参考文献
P.292 掲載の参考文献
1) Boder E, Sedgwick RP : Ataxia-telangiectasia. (Clinical and immunological aspects). Psychiatr Neurol Med Psychol Beih 13-14 : 8-16, 1970.
2) Swift M, et al : The incidence and gene frequency of ataxia-telangiectasia in the United States. Am J Hum Genet 39 : 573-583, 1986.
4) 森尾友宏 : Ataxia telangiectasiaの臨床的特徴-全国調査から明らかになったこと-. 小児科臨床 61 : 1805-1810, 2008.
7) 高木正稔 : DNA損傷応答と血液腫瘍. 臨床血液 51 : 539-545, 2010.
P.296 掲載の参考文献
1) Aldrich RA, et al : Pedigree demonstrating as ex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. Pediatrics 13 : 133-139, 1954.
2) Stray-Pedersen A, et al : Primary immunodeficiency diseases in Norway. J Clin Immunol 20 : 477-485, 2000.
6) Meyer-Bahlburg A, et al : Wiskott-Aldrich syndrome protein deficiency in B cells results in impaired peripheral homeostasis. Blood 112 : 4158-4169, 2008.
8) Mehmet D, et al : Eczematous skin lesions in an infant. Am Fam Physician 15 : 191-193, 2009.
9) Dupuis-Girod S, et al : Autoimmunity in Wiskott-Aldrich syndrome : risk factors, clinical features, and outcome in a single-center cohort of 55 patients. Pediatrics 111 : 622-627, 2003.
10) Ochs HD, et al : The Wiskott-Aldrich syndrome : studies of lymphocytes, granulocytes, and platelets. Blood 55 : 243-252, 1980.
P.299 掲載の参考文献
P.302 掲載の参考文献
1) Good RA : Agammaglobulinemia-a provocative experiments of nature. Bull Univ Minn Hosp 26 : 1-19, 1954.
3) 岩田力 : 原発性免疫不全症候群症例登録調査. 厚労省特定疾患血液疾患調査研究班 原発性免疫不全症候群分科会. 平成19年度研究業績報告書, 2007.
9) Watta RG, Kelly DR : Fatal varicella infection in a child associated with thymoma and immunodeficiency (Good's syndrome). Med Pediatr Oncol 18 : 246-251, 1990.
P.309 掲載の参考文献
2) Buckley RH, et al : Extreme hyperimmunoglobulinemia E and undue susceptibility to infection. Pediatrics 49 : 59-70, 1972.
3) 高田英俊, 峯岸克行 : 高IgE症候群の最近の話題. 日臨免疫会誌 33 : 15-19, 2010.
7) Minegishi Y, Takada T : Defects in Jak-STAT-mediated cytokine signals cause hyper-IgE syndrome : lessons from a primary immunodeficiency. Int Immunol 22 : 105-112, 2010.
9) Grimbercher B, et al : Genetic linkage of heper-IgE syndrome to chromosome 4. Am J Hum Genet 65 : 735-744, 1999.
P.316 掲載の参考文献
3) Richard BJ Jr : Disorder of the complement System. In : Nelson Textbook of Pediatrics, 19th ed, chapter 128, p753-756, 2011.
5) Laich A, Sim RB : Cross-talk between the human complement classical and alternative pathways : evidence for a C4bBb 'hybrid' C3 convertase. Mol Immunol 38 : 105, 2011.
6) Yang Y, et al : The intricate role of complement component C4 in human systemic lupus erythematosus. Curr Dir Autoimmun 7 : 98-132, 2004.
12) 原寿郎 : 先天性補体欠損症. 小児内科 40 (増刊号) : 1360-1364, 2008.
13) Takeda J, et al : Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell 73 : 703-711, 1993.
P.320 掲載の参考文献
P.325 掲載の参考文献

V 血小板の異常

P.332 掲載の参考文献
1) Thiele J, et al : Essential thrombocythaemia. In : WHO classification of tumours of haematopoietic and lymphoid tissues (ed by Swerdlow SH, et al), p48-50, IARC, Lyon, 2008.
8) Barbui T, et al : Philadelphila-negative classical myeloproliferative neoplasms : Critical concepts and management recommendations from European Leukemia Net. J Clin Oncol 29 : 761-770, 2011.
P.336 掲載の参考文献
1) Swerdlow SH, et al : WHO Classification of Tumors of Haematopoietic and Lymphoid Tissues, WHO, 4th ed, 2008.
7) Ishibashi T, et al : Thrombopoietic effects of interleukin-6 in long-term administration in mice. Exp Hematol 21 (5) : 640-646, 1993.
9) Ishida Y, et al : Purification of proplatelet formation (PPF) stimulating factor : thrombin/antithrombin III complex stimulates PPF of megakaryocytes in vitro and platelet production in vivo. Thromb Haemost 85 (2) : 349-355, 2001.
13) Broudy VC, et al : Thrombopoietin (c-mpl ligand) acts synergistically with erythropoietin, stem cell factor, and interleukin-11 to enhance murine megakaryocyte colony growth and increases megakaryocyte ploidy in vitro. Blood 85 (7) : 1719-1726, 1995.
14) Balcik OS, et al : Increased erythropoietin levels in reactive thrombocytosis. Haematologia 32 (1) : 59-65, 2002.
P.340 掲載の参考文献
2) 冨山佳昭 : 特発性血小板減少性紫斑病. 臨床血液 49 : 1298-1305, 2008.
4) 藤沢康司 : 特発性血小板減少性紫斑病 (小児) 血液疾患診療ハンドブック-診療の手引きと臨床データ集-改訂版 (吉田彌太郎編), p557-571, 医薬ジャーナル社, 2009.
5) 白幡聡ほか : 小児特発性血小板減少性紫斑病-診断・治療・管理ガイドライン-. 日小血会誌 18 : 210-218, 2004.
P.344 掲載の参考文献
2) 冨山佳昭ほか : ITP (特発性血小板減少性紫斑病) 研究報告. 厚生労働科学研究費補助金難治性疾患克服研究事業血液凝固異常症に関する調査研究 (主任研究者村田満). 平成20-22年度総括・分担研究報告書. p15-37, 2011.
3) McMillan R, et al : Platelet-associated and plasma anti-glycoprotein autoantibodies in chronic ITP. Blood 70 : 1040-1045, 1987.
7) Panitsa FP, et al : Adult chronic idiopathic thrombocytopenic purpura (ITP) is the manifestation of a type-1 polarized immune response. Blood 103 : 2645-2647, 2004.
8) Wang JD, et al : Reduced expression of transforming growth factor-β1 and correlated elevation of interleukin-17 and interferon-γ in pediatric patients with chronic primary immune thrombocytopenia (ITP). Pediatr Blood Cancer 57 : 636-640, 2011.
10) Fabis F, et al : Platelet-associated autoantibodies as detected by a solid-phase modified antigen capture ELISA test (MACE) are useful prognostic factor in idiopathic thrombocytopenic purpura. Blood 103 : 4562-4564, 2004.
17) Kuter DJ, et al : Efficacy of romiplostim in patients with chronic immune thombocytopenic purpura : a double-blind randomized controlled trial. Lancet 371 : 395-403, 2008.
18) 藤村欣吾ほか : 成人特発性血小板減少性紫斑病治療の参照ガイド 2012年版. 臨床血液 53 : 433-442, 2012.
P.350 掲載の参考文献
1) 日本小児血液学会疾患登録委員会 : 平成21年度日本小児血液学会疾患登録集計報告. 日小児血液会誌 24 : 182-189, 2010.
6) 今泉益栄 : 特発性血小板減少性紫斑病, あるいは免疫性血小板減少症 (ITP) を取り巻く最近の動向. 日小児血液会誌 25 : 8-16, 2011.
7) 白幡聡ほか : 小児特発性血小板減少性紫斑病-診断・治療・管理ガイドライン-. 日小児血液会誌 18 : 210-218, 2004.
11) 今泉益栄ほか : ITPに関する最近の展開. 日小血・がん会誌 49 : 373-381, 2012.
P.354 掲載の参考文献
1) 冨山佳昭 : 特発性血小板減少性紫斑病. 臨床血液 49 : 1298-1305, 2008.
4) 藤村欣吾ほか : 成人特発性血小板減少性紫斑病治療の参照ガイド 2012年版. 臨床血液 53 : 433-442, 2012.
7) 冨山佳昭 : トロンボポエチン受容体作動薬による難治性ITPの治療. 臨床血液 52 : 627-632, 2011.
P.357 掲載の参考文献
1) 川口千晴, 高橋幸博 : 周産期をめぐる血液-胎児・新生児編, 新生児血小板減少症. 周産期医学 33 : 356-360, 2003.
2) 白川嘉継, 白幡聡 : 症例から学ぶ自己免疫疾患, 新生児同種免疫性血小板減少症. 小児内科 36 : 1634-1637, 2004.
4) 大戸斉 : 抗血小板抗体. わかりやすい周産期・新生児の輸血療法 (大戸斉, 大久保光夫編), p143-147, メジカルビュー社, 2009.
5) 飯野美穂ほか : 本邦における新生児血小板減少症の集計調査. 日輸血細胞治療会誌 56 : 508-514, 2010.
10) 野村寿博ほか : HPA-3a抗原不適合による新生児同種免疫性血小板減少症の1例. 日小児会誌 113 : 857-860, 2009.
14) 橋本誠ほか : 抗HPA-1a抗体による新生児同種免疫性血小板減少症の対応. 日輸血細胞治療会誌 56 : 648-650, 2010.
15) 松橋美佳 : 輸血に関連した血小板の検査. 検査と技術 38 : 848-851, 2010.
P.362 掲載の参考文献
3) Selling S, et al : Heparin-induced thrombocytopenia in patients requiring prolonged intensive care unit treatment after cardiopulmonary bypass. J Thromb Haemost 6 : 428-435, 2008.
10) 松尾武文 : ヘパリン起因性血小板減少症-その病態と治療. 臨床血液 43 (6) : 464-467, 2002.
P.367 掲載の参考文献
6) Lopez JA, et al : The glycoprotein Ib-IX complex-specific monoclonal antibody SZ1 binds to a conformation-sensitive epitope on glycoprotein IX : implications for the target antigen of quinine/quinidine-dependent autoantibodies. Blood 85 (5) : 1254-1258, 1995.
7) Chong BH, et al : Characterization of the binding domains on platelet glycoproteins Ib-IX and IIb/IIIa complexes for the quinine/quinidine-dependent antibodies. Blood 77 (10) : 2190-2199, 1991.
8) Curtis BR, et al : Antibodies in sulfonamide-induced immune thrombocytopenia recognize calcium-dependent epitopes on the glycoprotein IIb/IIIa complex. Blood 84 (1) : 176-183, 1994.
9) Visentin GP, et al : Characteristics of quinine- and quinidine-induced antibodies specific for platelet glycoproteins IIb and IIIa. Blood 77 (12) : 2668-2676, 1991.
P.371 掲載の参考文献
1) Moschcowitz E : Hyaline thrombosis of the terminal arterioles and capillaries : A hitherto undescribed disease. Pro N Y Pathol Soc 24 : 21-24, 1924.
4) Furlan M, et al : Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis. Blood 87 : 4223-4234, 1996.
5) Tsai HM : Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion. Blood 87 : 4235-4244, 1996.
7) Levy GG, et al : Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 413 : 488-494, 2001.
P.374 掲載の参考文献
11) 國島伸治 : 先天性巨大血小板症の鑑別診断. 血栓止血誌 22 : 100-106, 2011.
P.379 掲載の参考文献
1) Lacombe M, D'angelo G : Etudes sur une thrombopathie familial. Nouv Rev Fr Hematol 3 : 611-614, 1963.
2) Milton JG, Frojmovic MM : Shape-changing agents produce abnormally large platelets in a hereditary "giant platelet syndrome (mps)". J Lab Clin Med 93 : 154-161, 1979.
3) Milton JG, et al : Spontaneous platelet aggregation in a hereditary giant platelet syndrome (MPS). Am J Pathol 114 : 336-345, 1984.
4) Okita JR, et al : Montreal platelet syndrome : A defect in calcium-activated neutral proteinase (calpain). Blood 74 : 715-721, 1989.
7) 嶋緑倫 : von Willebrand病. 血液専門医テキスト (日本血液学会編集), p391-393, 南江堂, 2011.
8) 國嶋伸治 : 先天性巨大血小板症の鑑別診断. 血栓止血誌 22 : 100-106, 2011.
11) Bernard J, Soulier JP : Sur une nouvelle variete dedystrophie thrombocttaire hemorrhagipare congenital. Sem Hop Paris 24 : 3217-3223, 1948.
12) Lecher K, et al : May-Hegglinshe Anomalie. Acta Haematol 42 : 303-320, 1969.
14) Miller JL, Castalla A : Platelet-type von Willebrand's disease : Characterization of a new bleeding disorder. Blood 60 : 790-794, 1982.
P.382 掲載の参考文献
7) 國島伸治 : 先天性巨大血小板症の鑑別診断. 血栓止血誌 22 : 100-106, 2011.
8) Greinacher A, Mueller-Eckhardt C : Hereditary types of thrombocytopenia with giant platelets and inclusion bodies in the leukocytes. Blut 60 : 53-60, 1990.
P.385 掲載の参考文献
1) Peterson LC, et al : Fechtner syndrome-a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia. Blood 65 : 397-406, 1985.
9) 國島伸治 : 先天性巨大血小板症の鑑別診断. 血栓止血誌 22 : 100-106, 2011.
P.388 掲載の参考文献
P.391 掲載の参考文献
6) Martino R, et al : Combined autoimmune cytopenias. Haematologica 80 (4) : 305-310, 1995.
11) Bucaneve G, et al ; Gruppo Italiano Malattie Ematologiche dell' Adulto (GIMEMA) Infection Program : Levofloxacin to prevent bacterial infection in patients with cancer and neutropenia. N Engl J Med 353 : 977-987, 2005.
P.395 掲載の参考文献
2) Schiffer CA, et al : Platelet transfusion for patients with cancer : clinical practice guidelines of American Society of Clinical Oncology. J Clin Oncol 19 : 1519-1538, 2001.
4) 榎本隆行ほか : 妊娠による血小板反応性抗体 (HLA抗体とhuman platelet antigens抗体) の産生. 日輸血会誌 46 : 467-473, 2000.
5) 永尾暢夫 : HLA適合血小板の供給. 日輸血会誌 43 : 30-33, 1997.
6) Pappalardo P, et al : Platelet transfusion refractoriness associated with HPA-1a (PIA1) alloantibody without coexistent HLA antibodies successfully treated with antigen-negative platelet transfusion. Transfusion 41 : 984-987, 2002.
P.402 掲載の参考文献
1) Bernard J, Soulier JP : Sur une nouvelle variete de dystrophie thrombocytaire-hemorragipare congenitale. Sem Hop 24 : 3217-3223, 1948.
5) Cunningham JG, et al : The cytoplasmic domain of the α-subunit of glycoprotein (GP) Ib mediates attachment of the entire GP Ib-IX complex to the cytoskeleton and regulates von Willebrand factor-induced changes in cell morphology. J Biol Chem 271 : 11581-11587, 1996.
7) Kurokawa Y, et al : A missense mutation (Tyr88 to Cys) in the platelet membrane glycoprotein Ibβ gene affects GPIb/IX complex expression : Bernard-Soulier syndrome in the homozygous form and giant platelets in the heterozygous form. Thromb Haemost 86 : 1249-1256, 2001.
9) Poujol C, et al : Absence of GPIbαis responsible for aberrant membrane development during megakaryocyte maturation : ultrastructural study using a transgenic model. Exp Hematol 30 : 352-360, 2002.
11) 國島伸治 : 先天性巨大血小板症の鑑別診断. 血栓止血誌 22 : 100-106, 2011.
14) Rieger C, et al : Allogeneic stem cell transplantation as a new treatment option for patients with severe Bernard-Soulier Syndrome. Thromb Haemost 95 : 190-191, 2006.
P.406 掲載の参考文献
9) Shiozaki H, et al : Auto antibodies neutralizing thrombopoietin in a patient with amegakaryocytic thrombocytopenic purpura. Blood 95 : 2187, 2000.
12) Guinan EC, et al : Effects of interleukin-3 and granulocyte-macrophage colony-stimulating factor on tyhrombopoiesis in congenital amegakaryocytic thrombocytopenia. Blood 81 : 1691, 1993.
P.411 掲載の参考文献
1) Shreiner DP, Bell WR : Pseudothrombocytopenia : Manifestation of a new type of platelet agglutinin. Blood 42 : 541-549, 1973.
4) Bizzaro N : EDTA-dependent pseudothrombocytopenia : A clinical and epidemiological study of 112 cases, with 10-year follow-up. Am J Hematol 50 : 103-109, 1995.
5) Onder O, et al : Pseudothrombocytopenia caused by platelet agglutinins that are reactive in blood anticoagulated with chelating agents. Blood 56 : 177-182, 1980.
9) 西郷勝康ほか : EDTA依存性偽性血小板減少症の抗血小板抗体の認識する抗原について. 臨床血液 27 : 1305-1309, 1986.
P.415 掲載の参考文献
P.418 掲載の参考文献
2) Holmsen H, Weiss HJ : Further evidence for a deficient storage pool of adenine nucleotides in platelets from some patients with thrombocytopathia- "storage pool disease". Blood 39 : 197-209, 1972.
3) Nieuwenhuis HK, et al : Patients with a prolonged bleeding time and normal aggregation tests may have storage pool deficiency : studies on one hundred six patients. Blood 70 : 620-623, 1987.
4) Weiss HJ, Ames RP : Ultrastructural findings in storage pool disease and aspirin-like defects of platelets. Am J Pathol 71 : 447-466, 1973.
P.423 掲載の参考文献
1) Yasunaga K : Congenital platelet function disorders : survey findings and pathophysiology. Nihon Ketsueki Gakkai Zasshi 49 : 1499-1508, 1986.
3) Wagner CL, et al : Analysis of GPIIb/IIIa receptor number by quantification of 7E3 binding to human platelets. Blood 88 : 907-914, 1996.
4) O'Toole TE, et al : Efficient surface expression of platelet GPIIb-IIIa requires both subunits. Blood 74 : 14-18, 1989.
5) Kottke-Marchant K, Corcoran G : The laboratory diagnosis of platelet disorders. Arch Pathol Lab Med 126 : 133-146, 2002.
6) Tomiyama Y : Glanzmann thrombasthenia : integrin alpha IIb beta 3 deficiency. Int J Hematol 72 : 448-454, 2000.
7) George JN, et al : Glanzmann's thrombasthenia : the spectrum of clinical disease. Blood 75 : 1383-1395, 1990.
9) Kiefel V, et al : [Neonatal isoimmune thrombocytopenia by anti-GPIIb/IIIa]. Beitr Infusionsther 30 : 450-453, 1992.
12) Poon MC, et al : Recombinant factor VIIa is effective for bleeding and surgery in patients with Glanzmann thrombasthenia. Blood 94 : 3951-3953, 1999.
P.427 掲載の参考文献
7) Kamata T, et al : Plateletintegrin αIIbβ3-ligand interactions : what can we learn from the structure? Int J Hematol 74 : 382-389, 2001.
8) Peyruchaud O, et al : R to Q substitution in the GFFKR sequence of the cytoplasmic domain of the integrin alphaIIb subunit in a patient with a Glanzmann's thrombasthenia-like syndrome. Blood 92 : 4178-4187, 1998.
9) Nurden AT, et al : Glanzmann thrombasthenia-like syndromes associated with Macrothrombocytopenias and mutations in the genes encoding the αIIbβ3 integrin. Semin Thromb Hemost 37 : 698-706, 2011.
15) Fang J, et al : Platelet gene therapy improves hemostatic function for integrin αIIbβ3-deficient dogs. Proc Natl Acad Sci USA 108 : 9583-9588, 2011.
P.431 掲載の参考文献
1) Hermansky F, Pudlak P : Albinism associated with hemorrhagic diathesis and unusual pigmented reticular cells in the bone marrow : report of two cases with histochemical studies. Blood 14 : 162-169, 1959.
3) Davies BH, Tuddenham EGD : Familial pulmonary fibrosis associated with oculocutaneous albinism and platelet function defect. A new syndrome. Q J Med 45 : 219-232, 1976.
5) 木村定勝ほか : Hermansky-Pudlak症候群の1例. 日皮会誌 103 : 805-813, 1993.
9) 近藤光子, 角田裕美 : Hermansky-Pudlak症候群. 呼吸器科 5 : 149-154, 2004.
10) 鈴木民夫 : Hermansky-Pudlak syndrome. Clinical Dermatology 60 : 23-26, 2006.
12) Sherman A, et al : Perirectal abscess in the Hermansky-Pudlak syndrome with granulomatous colitis in children. Am J Gastroenterol 84 : 552-556, 1989.
P.435 掲載の参考文献
14) Fuse I, et al : Defective signal transduction induced by thromboxane A2 in a patient with a mild bleeding disorder : impaired phospholipase C activation despite normal phospholipase A2 activation. Blood 81 (4) : 994-1000, 1993.
P.438 掲載の参考文献
P.443 掲載の参考文献
3) Bolton-Maggs PH, et al : A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO. Br J Haematol 135 : 603-633, 2006.
4) Weiss HJ, Lages B : Family studies in Scott syndrome. Blood 90 : 475-476, 1997.
5) Toti F, et al : Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder. Blood 87 : 1409-1415, 1996.
8) Rosing J, et al : Impaired factor X and prothrombin activation associated with decreased phospholipid exposure in platelets from a patient with a bleeding disorder. Blood 65 : 1557-1561, 1985.
9) Sims PJ, et al : Assembly of the platelet prothrombinase complex is linked to vesiculation of the platelet plasma membrane. Studies in Scott syndrome : an isolated defect in platelet procoagulant activity. J Biol Chem 264 : 17049-17057, 1989.
P.445 掲載の参考文献
P.449 掲載の参考文献
2) Gronich JH, et al : Identification and characterization of a hormonally regulated form of phospholipase A2 in rat renal mesangial cells. J Biol Chem 263 : 16645-16651, 1988.
3) Gijon MA, et al : Role of phosphorylation sites and the C2 domain in regulation of cytosolic phospholipase A2. J Cell Biol 145 : 1219-1232, 1999.
6) Adler DH, et al : Inherited human cPLA2α deficiency is associated with impaired eicosanoid biosynthesis, small intestinal ulceration, and platelet dysfunction. J Clin Invest 118 : 2121-2131, 2008.
9) Okuma M : Platelet function and arachidonate metabolism in patients with chronic myeloproliferative disorders. Acta Haematol Jpn 43 : 1139-1144, 1980.
10) Jubelirer SJ, et al : Platelet arachidonic acid metabolism and platelet function in ten patients with chronic myelogenous leukemia. Blood 56 : 728-731, 1980.
P.454 掲載の参考文献
8) ESPRIT Study Group, Halkes PH, et al : Aspirin plus dipyridamole versus aspirin alone after cerebral ischaemia of arterial origin (ESPRIT) : randomised controlled trial. Lancet 367 (9523) : 1665, 2006.
9) 金子誠, 矢冨裕 : 血小板機能異常症の診断と対応. 日血栓止血会誌 20 (5) : 487-494, 2009.
P.457 掲載の参考文献
1) 日本血栓止血学会用語集 (血小板) Glanzmann血小板無力症 [http://www.jsth.org/term/kesshoban.html#04]
2) Glanzmann WE : Hereditare hamorrhagische Thrombasthenie. Ein Beitrag zur Pathologie der Blutplattchen. Jahrbuch fur Kinderheilkunde 88 : 1-42, 113-141, 1918.
3) 渡辺清明 : 血小板機能異常. 日内会誌 80 : 46-51, 1991.
4) 金子誠, 矢冨裕 : 血小板機能異常の診断と対応. 血栓止血誌 20 : 487-494, 2009.
6) Levy-Toledano S, et al : Acquired IgG antibody occurring in a thrombasthenic patient : its effect on human platelet function. Blood 51 : 1065-1072, 1978.
8) Niessner H, et al : Acquired trombasthenia due to GPIIb/IIIa-specific platelet autoantibodies. Blood 68 : 571-576, 1986.

VI 血管障害による出血傾向

P.464 掲載の参考文献
3) Grand' Maison A : Hereditary hemorrhagic telangiectasia. CMAJ 180 (8) : 833-835, 2009.
4) Mc Allister KA, et al : Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet 8 : 345-351, 1994.
P.468 掲載の参考文献
1) Malfait F, et al : Ehlers-Danlos Syndrome, Classic Type. Synonym : Ehlers-Danlos Syndrome, Classical Type. Includes : Ehlers-Danlos Syndrome Type I, Ehlers-Danlos Syndrome Type II. GeneReviews(TM) [Internet]. Seattle (WA) : University of Washington, Seattle ; 1993-. Initial Posting : September 2, 1999 ; Last Update : May 3, 2011.
2) Levy HP, et al : Ehlers-Danlos Syndrome, Hypermobility Type Synonyms. Synonym : EDS Hypermobility Type, EDS Type III, Ehlers-Danlos Syndrome Type III. GeneReviews(TM) [Internet]. Seattle (WA) : Universityof Washington, Seattle ; 1993-. Initial Posting : October 22, 2004.
3) Pepin MG, Byers PH : Ehlers-Danlos Syndrome Type IV. Synonyms : EDS Type IV ; Ehlers-Danlos Syndrome, Vascular Type. GeneReviews(TM) [Internet]. Seattle (WA) : University of Washington, Seattle ; 1993-. Initial Posting : September2, 1999 ; Last Update : May 3, 2011.
5) Beighton P, et al : Ehlers-Danlossyndromes : revisednosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK). Am J Med Genet 7 : 31-37, 1998.
6) Leistritz DF, et al : COL3A1 haploinsufficiency results in EDS type IV with delayed onset of complications and longer life span when compared to missense and splice-site mutations. Poster session 1670, Washington, DC : American Societyof Human Genetics 60th Annual Meeting, 2010.
P.471 掲載の参考文献
2) 河野照隆 : DNA自己感作性紫斑病. 感染・炎症・免疫 16 : 132-137, 1986.
3) Brauner F, et al : Autosensitization to DNA. Acta Derm Venereol 60 : 345-348, 1980.
4) Rodriguez Fernandez JM, Linares Ruiz MS : DNA autosensitivity ; report of two cases. Sangre (Barc) 26 : 114-122, 1981.
5) Sugai S, et al : A case of DNA autosensitivity. Arerugi 31 : 9-17, 1982.
9) Gardner FH, Diamond LK : Autoerythrocyte sensitization ; a form of purpura producing painful bruising following autosensitization to red blood cells in certain women. Blood 10 : 675-690, 1955.
12) Parker FS, Irvin JL : The interaction of chloroquine with nucleic acid and nucleoproteins. J Biol Chem 199 : 897-909, 1952.
P.473 掲載の参考文献
1) Gardner FH, Diamond LK : Autoerythrocyte sensitization : a form of purpura producting painful brusing following autosensitization to red blood cells in certain women. Blood 10 : 675-690, 1955.
3) Ratnoff OD : The psychogenic purpuras : review of autoerythrocyte sensitization, autosensitization to DNA, "hysterial" and factitial bleeding, and the religious stigmata. Semin Hematol 17 : 192-213, 1980.
4) Hawsawi KA, Pope E : Pediatric psychocutaneous disorders : a review of primary psychiatric disorders with dermatologic manifestations. Am J Clin Dermatol 12 : 247-257, 2011.
5) Kremer WB, et al : Recurrent ecchymoses and cutaneous hyperactivity of hemoglobin : a form of autoerythrocyte sensitization. Blood 30 : 62-73, 1967.
7) Durmazlar SP, et al : Is Gardner-Diamond syndrome associated with hormonal influences along with psychosocial problems? A delayed diagnosis. Eur J Dermatol 19 : 259-260, 2009.
10) Silney W, et al : Gardner-Diamond syndrome. Int J Dermatol 49 : 1178-1181, 2010.
P.476 掲載の参考文献
1) Cox NH, Piette WW : Purpura and microvascular occlusion. In : Rook's Textbook of Dermatology (ed by Burns T, et al), 7th ed, Blackwell Science, Massachusetts, 2004.
2) 塚本克彦 : 血管性紫斑. 紅斑・滲出性紅斑紫斑脈管系の疾患最新皮膚科学大系 4 (玉置俊彦編), 中山書店, 2003.
4) Shibli-Rahhal A, et al : Cushing's syndrome. Clin Dermatol 24 (4) : 260-265, 2006.
P.479 掲載の参考文献
1) Scurvy and its prevention and control in major emergencies. World Health Organization, United Nations High Commissioner for Refugees, 1999.
2) 厚生労働省「日本人の食事摂取基準について」, 第6次改定「日本人の栄養所要量」, 1999.
5) 間瀬勘史 : 壊血病, Moller-Barlow病. 別冊日本臨牀 血液症候群 (II), p405-407, 日本臨牀社, 1998.
P.483 掲載の参考文献
1) Jennette JC, et al : Nomenclature of systemic vasculitides. Proposal of an international consensus conference. Arthritis Rheum 37 : 187-192, 1994.
12) Reamy BV, et al : Henoch-Schonlein purpura. Am Fam Physician 80 : 697-704, 2009.
P.487 掲載の参考文献
1) Sunderkotter C, Sindrilaru A : Clinical classification of vasculitis. Eur J Dermatol 16 : 114-124, 2006.
3) Jennette JC, et al : Nomenclature of systemic vasculitides. Proposal of an international consensus conference. Arthritis Rheum 37 : 187-192, 1994.
4) 永渕裕子, 山田秀裕 : 過敏性血管炎. 日本臨牀 67 (11) : 2148-2151, 2009.
7) Stein JC, et al : Necrotizing vasculitis as a complication of propylthiouracil. West J Emerg Med 9 : 212-215, 2008.
10) Radic M, et al : Drug-induced vasculitis : a clinical and pathological review. Neth J Med 70 : 12-17, 2012.
11) Stone J : Immune complex-mediated small vessel vasculitis. In : Kelley's Textbook of Rheumatology 8th ed II (ed by Firestein G, et al), p1465-1473, W. B. Saunders, Philadelphia, 2008.
P.489 掲載の参考文献
P.491 掲載の参考文献
1) Rees MM, Rodgers GM : Bleeding disorders caused by vascular abnormalities. In : Wintrobe's Clinical Hematology, 12th ed (ed by Pine JW Jr), p1335-1351, Lippincott W & W, Philadelphia, 2009.
3) Shuster S, Scarborough H : Senile purpura. Q J Med 30 : 33-40, 1961.

VII 凝固・線溶異常による出血傾向

P.498 掲載の参考文献
1) Bloom AL (ed) : Introduction. In : The Hemophilia, p1, Churchill Livingstone, Philadelphia, 1982.
2) 血液凝固異常症全国調査運営委員会 : 厚生労働省委託事業血液凝固異常症全国調査平成23年度報告書, p3, 公益財団法人エイズ予防財団, 2012.
3) Kemball-Cook G, et al : The factor VIII Structure and Mutation Resource Site : HAMSTeRS version 4. Nucleic Acids Res 26 : 216-219, 1998.
4) 三間屋純一 : II. 診断 1. 臨床症状. みんなに役立つ血友病の基礎と臨床 (白幡聡編), p106-116, 医薬ジャーナル社, 2009.
6) 西田恭治 : 2 出血症状に対する治療法 (5) 消化管出血. ヘモフィリア治療の最前線, 血友病の診断と治療 (吉岡章編), p58-63, 医科学出版社, 2002.
8) Schulman S : Mild Hemophilia, p2, World Federation of Hemophilia, Montreal, 2006.
9) Huth-Kuhne A, et al : International recommendation on the diagnosis and treatment of patients with acquired hemophilia A. Haemoatologica 94 : 566-575, 2009.
10) 松下正ほか : インヒビターのない血友病患者の急性出血, 処置・手術における凝固因子補充療法のガイドライン. 日血栓止血会誌 19 : 510-519, 2008.
11) 田中一郎ほか : インヒビター保有先天性血友病患者に対する止血治療ガイドライン. 日血栓止血会誌 19 : 520-529, 2008.
P.503 掲載の参考文献
2) 奥村薫, 小嶋哲人 : 3. 血友病の病態 4) 血友病Bの分子生物学. みんなに役立つ血友病の基礎と臨床 (白幡聡編), p52-59, 医薬ジャーナル社, 2009.
3) Bloom AL (ed) : Introduction. In : The Hemophilia, p1, Churchill Livingstone, Philadelphia, 1982.
4) 血液凝固異常症全国調査運営委員会 : 厚生労働省委託事業血液凝固異常症全国調査平成23年度報告書, p3-12, 公益財団法人エイズ予防財団, 2012.
6) Klamroth R, et al : Haemophilia A and haemophilia B. Are there relevant clinical differences? Hamostaseologie 30 (Suppl 1) : S26-27, 2010.
9) 松下正ほか : インヒビターのない血友病患者の急性出血, 処置・手術における凝固因子補充療法のガイドライン. 日血栓止血会誌 19 : 510-519, 2008.
10) 田中一郎ほか : インヒビター保有先天性血友病患者に対する止血治療ガイドライン. 日血栓止血会誌 19 : 520-529, 2008.
P.506 掲載の参考文献
1) Nishino M, et al : New variant of von Willebrand disease with defective binding to factor VIII. Blood 74 : 1591-1599, 1989.
4) Sadler JE : A revised classification of von Willebrand disease. Thromb Haemost 71 : 520-525, 1994.
5) Foster PA, etal : A major factor VIIIb dinding dmain residues inding domainresidues with intheamino-terminal 272 amino acid residues of von Willebrand factor. J Biol Chem 262 : 8443-8446, 1987.
7) 嶋緑倫 : 第VIII因子結合能異常症. 別冊日本臨牀 血液症候群 II, p430-433, 日本臨牀社, 1998.
P.508 掲載の参考文献
6) Hayashi H, et al : Molecular genetic survey of five Japanese families with high-molecular weight kininogen deificiency. Blood 75 : 1296-1304, 1990.
9) Cheung PP, et al : Genetic basis of total kininogen deficiency in Williams' trait. J Biol Chem 268 : 23361-23365, 1993.
10) Davidoson SJ, et al : High molecular weight kininogen deficiency : a patient who underwent cardiac surgery. Thromb Haemost 85 : 195-197, 2001.
P.511 掲載の参考文献
1) Lowenberg EC, et al : Coagualtion factor XI as a novel target for antithrombotic treatment. J Thromb Haemost 8 : 2349-2357, 2010.
3) Oeri J, et al : Congenital factor V deficiency (parahemophilia) with true hemophilia I two brothers. Bibl Paediatr 58 : 575-588, 1954.
11) Bolton-Maggs PHB, et al : The rare coagulation disorders-review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation. Haemophilia 10 : 593-628, 2004.
P.515 掲載の参考文献
7) Castol di E, et al : A missensemutation (Y1702C) inthecoagulationfactor V gene is a frequent cause of factor V deficiency in the Italian population. Haematologica 86 : 629-633, 2001.
9) Bolton-Maggs PHB, et al : The rare coagulation disorders-review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation. Haemophilia 10 : 593-628, 2004.
11) Gonzalez-Boullosa R, et al : The use of activated recombinant coagulation factor VII during haemarthroses and synovectomy in a patient with congenitalseverefactor V deficiency. Haemophilia 11 : 167-170, 2005.
P.520 掲載の参考文献
10) Reddy SV, et al : Molecular characterization of human Factor XSan Antonio. Blood 74 : 1486-1490, 1989.
11) Menegatti M, Pewandi F, et al : Factor X deficiency. Semin Thromb Hemost 35 : 407-415, 2009.
P.523 掲載の参考文献
3) Mc Mullen BA, et al : Location of the disulfide bonds in human coagulation factor XI : the presence of tandem apple domains. Biochemistry 30 : 2056-2060, 1991.
6) Naito K, et al : Activation of human blood coagulation factor XI independent of factor XII. J Biol Chem 266 : 7353-7358, 1991.
8) vondem Borne P, et al : Feedback activation of factor XI by thrombin in plasma results in additional formation of thrombin that protects fibrin clots from fibrinolysis. Blood 86 : 3035-3042, 1995.
14) Seligsohn U, Modan M : Definition of the population at risk of bleeding due to factor XI deficiency in Ashkenazic Jews and the value of activated partial thromboplastin time in its detection. Isr J Med Sci 17 : 413-415, 1981.
P.529 掲載の参考文献
1) Hantgan RR, et al : Fibrinogen structure and physiology. In : Hemostasis and Thrombosis, 4th ed (ed by Colman RW, et al), p203-232, Lippincott Williams & Wilkins, Philadelphia, 2001.
2) 諏合輝子 : フィブリノゲンの基礎と臨床. 図説 血栓・止血・血管学 (一瀬白帝編), p280-285. 中外医学社, 2005.
3) Tuddenham ED, Cooper DN : Fibrinogen. In : The Molecular Genetics of Haemostasis and Its Inherited Disorders, p248-270, Oxford Medical Publications, NY, 1994.
4) 小林隆夫ほか : 先天性無フィブリノゲン血症-妊娠・分娩管理を中心に-. 日血栓止血会誌 12 : 57-65, 2001.
9) 松田道生ほか : 遺伝性異常フィブリノゲン血症. 日血栓止血会誌 12 : 47-56, 2001.
P.532 掲載の参考文献
4) Inomoto T, et al : Prothrombin Tokushima : characterization of dysfunctional thrombin derived a variant of human prothrombin. Blood 69 : 565-569, 1987.
6) http://www.isth.org/default/index.cfm/publications/registries-databases/mutations-rare-bleeding-disorders/ (2012年9月1日にアクセス).
7) Miyata T, et al : A point mutation (Arg271→Cys) of a homozygote for dysfunctional prothrombin, prothrombin Obihiro, which has a region of high sequence variability. Br J Haematol 90 : 688-692, 1995.
8) Morishita E, et al : Prothrombin Himi : a compound heterozygote for two dysfunctional prothrombin molecules (Met-337→Thr and Arg-388→His). Blood 80 : 2275-2280, 1992.
9) 森下英里子ほか : 先天性複合へテロ接合体プロトロンビン欠乏症の一例. 臨床血液 48 : 848, 1992.
10) 瀧正志 : 血液凝固異常症全国調査平成23年度報告書, p9, 公益財団法人エイズ予防財団, 2011.
11) Rabiet MJ, et al : Molecular defect of prothrombin Barcelona. Substitution of cysteine for arginine at residue 273. J Biol Chem 261 : 15045-15048, 1986.
P.537 掲載の参考文献
1) 一瀬白帝 : 血液凝固と凝固制御機構. 臨床検査 55 : 328-339, 2011.
4) Mariani G, et al : International Factor VII Deficiency Study Group : Clinical phenotypes and factor VII genotype in congenital factor VII deficiency. Thromb Haemost 93 : 481-487, 2005.
6) 一瀬白帝 : 表紙の図. 図説・分子病態学 第4版 (一瀬白帝・鈴木宏治 (編) ), 中外医学社, 2008.
P.543 掲載の参考文献
8) Hashiguchi T, et al : Two genetic defects in a patient with complete deficiency of the b-subunit for coagulation factor XIII. Blood 82 : 145-150, 1993.
9) Izumi T, et al : Type I factor XIII deficiency is caused by a genetic defect of its b subunit : insertion of triplet AAC inexon III leads to premature termination in the second Sushi domain. Blood 87 : 2769-2774, 1996.
15) Ichinose A : As many as 12 cases with hemorrhagic acquired factor XIII deficiency due to its inhibitors were recently found in Japan. Thromb Haemost 105 : 925-927, 2011.
P.548 掲載の参考文献
1) Colman RW, Schmaier AH : Contact system : a vascular biology modulator with anticoagulant, profibrinolytic, antiadhesive, and proinflammatory attributes. Blood 90 : 3819-3843, 1997.
3) Renne T, et al : Mapping of discontinuous h-kininogen binding site of plasma prekallikrein. J Biol Chem 274 : 25777-25784, 1999.
5) Ichinose A, et al : The activation of pro-urokinase by plasma kallikrein and its inactivation by thrombin. J Biol Chem 261 : 3486-3489, 1986.
7) Shigekiyo T, et al : Prekallikrein (PK) Tokushima : PK deficiency caused by a Gly401→Glu mutation. J Thromb Haemost 1 : 1314-1316, 2003.
8) 長屋聡美ほか : 高齢になってから診断された先天性プレカリクレイン欠乏症の1症例. 日老医誌 46 : 348-351, 2009.
10) Francois D, et al : Severe prekallikrein deficiency due to homozygous C529Y mutations. Blood Coagul Fibrinolysis 8 : 283-286, 2007.
P.554 掲載の参考文献
1) 瀧正志 : 血液凝固異常症全国調査平成23年度報告書, p3, 公益財団法人エイズ予防財団, 2012.
4) Hagiwara T, et al : Female hemophilia B with homozygous missense mutation p.Ala337Val in the factor IX gene. 臨床血液 (abstract) 52 : 1180, 2011.
5) Vencesla A, et al : Severe haemophilia A in a female resulting from an inherited gross deletion and a de novo codon deletion in the F8gene. Haemophilia 14 : 1094-1098, 2008.
7) Chuansumrit A, et al : Inversion of intron 22 of the factor VIII gene in a girl with severe hemophilia A and Turner's syndrome. Thromb Haemost 82 : 1379, 1999.
9) Loreth RM, et al : Haemophilia A in a female caused by coincidence of a Swyer syndrome and a missense mutation in factor VIII gene. Thromb Haemost 95 : 747-748, 2006.
10) Favier R, et al : Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female. Blood 96 : 4373-4375, 2000.
14) Nishino M, et al : New variant of von Willebrand disease with defective binding to factor VIII. Blood 74 : 1591-1599, 1989.
15) Allen RC, et al : Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet 51 : 1229-1239, 1992.
P.556 掲載の参考文献
3) Magallon M, et al : Hemophilic pseudotumor : multicenter experience over 25-year period. Am J Hematol 45 : 103-108, 1994.
4) 川中正雄ほか : 幼児に生じた下顎骨血友病性偽腫瘍の1例. 日口腔科会誌 46 : 414-418, 1997.
5) Rodriguez-Merchan EC : The haemophilic pseudotumour. Haemophilia 8 : 12-18, 2002.
6) Rodriguez-Merchan EC : Haemophilic cysts (pseudotumours). Haemophilia 8 : 393-401, 2002.
8) 竹谷英之 : 血友病性関節症と血友病性偽腫瘍. 整形・災害外科 48 : 1247-1254, 2005.
9) 竹谷英之ほか : 血友病性偽腫瘍の手術治療. 関節外科 21 : 603-606, 2002.
10) 松下正ほか : インヒビターのない血友病患者の急性出血, 処置・手術における凝固因子補充療法のガイドライン. 日血栓止血会誌 19 : 510-519, 2008.
11) 田中一郎ほか : インヒビター保有先天性血友病患者に対する止血治療ガイドライン. 日血栓止血会誌 19 : 520-539, 2008.
P.562 掲載の参考文献
1) von Willebrand E : Hereditar pseudohemophili. Fin Laekaresaellsk Hand 68 : 87-112, 1926.
5) Rodeghiero F, et al : Epidemiological investigation of the prevalence of von Willebrand's disease. Blood 69 : 454-459, 1987.
12) Rehemtulla A, Kaufman RJ : Preferred sequence requirements for cleavage of pro-von Willebrand factor by propeptide-processing enzymes. Blood 79 : 2349-2355, 1992.
15) Cramer EM, et al : Eccentric localization of von Willebrand factor in an internal structure of platelet alpha-granule resembling that of Weibel-Palade bodies. Blood 66 : 710-713, 1985.
20) Mancuso DJ, et al : Structure of the gene for human von Willebrand factor. J Biol Chem 264 : 19514-19527, 1989.
24) Gill JC, et al : The effect of ABO blood group on the diagnosis of von Willebrand disease. Blood 69 : 1691-1695, 1987.
25) Eikenboom JC, et al : Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor. Blood 88 : 2433-2441, 1996
27) The Diagnosis, Evaluation, and Management of von Willebrand disease. National Institutes of Health, National Heart, Lung, and Blood Institute, Bethesda, 2007.
P.567 掲載の参考文献
3) O'Brien LA, et al : Theoretical structural explanation for Group I and Group II, type2A von Willebrand disease mutations. J Thromb Haemost 3 : 796-797, 2005.
5) Gaucher C, et al : Characterization of von Willebrand factor gene defects in two unrelated patients with type IIC von Willebrand disease. Blood 84 : 1024-1030, 1994.
6) Schneppenheim R, et al : Defective dimerization of von Willebrand factor subunits due to a Cys→Arg mutation in type IID von Willebrand disease. Proc Natl Acad Sci USA 93 : 3581-3586, 1996.
11) Fujimura Y, et al : von Willebrand factor. A reduced and alkylated 52/48-kDa fragment beginning at amino acid residue 449 contains the domain interacting with platelet glycoprotein Ib. J Biol Chem 261 : 381-385, 1986.
15) Rabinowitz I, et al : Type IIB mutation His-505→Asp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib. J Biol Chem 268 : 20497-20501, 1993.
16) Vlot AJ, et al : The affinity and stoichiometry of binding of human factor VIII to von Willebrand factor. Blood 85 : 3150-3157, 1995.
17) Vlot AJ, et al : Kinetics of factor VIII-von Willebrand factor association. Blood 87 : 1809-1816, 1996.
18) Lollar P, et al : Association of the factor VIII light chain with von Willebrand factor. J Biol Chem 263 : 10451-10455, 1988.
19) Leyte A, et al : Sulfation of Tyr1680 of human blood coagulation factor VIII is essential for the interaction of factor VIII with von Willebrand factor. J Biol Chem 266 : 740-746, 1991.
20) Nishino M, et al : New variant of von Willebrand disease with defective binding to factor VIII. Blood 74 : 1591-1599, 1989.
21) Mazurier C, et al : A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction. Blood 75 : 20-26, 1990.
24) Takahashi H, et al : Substitution of Val for Met at residue 239 of platelet glycoprotein Ib alpha in Japanese patients with platelet-type von Willebrand disease. Blood 85 : 727-733, 1995.
P.571 掲載の参考文献
P.573 掲載の参考文献
6) Shigekiyo T, et al : Histidine-rich glycoprotein (HRG) Tokushima 2 : novel HRG deficiency, molecular and cellular characterization. Thromb Haemostas 84 : 675-679, 2000.
7) Shigekiyo T, et al : HRG Tokushima : molecular and cellular characterization of histidine-rich glycoprotein (HRG) deficiency. Blood 91 : 128-133, 1998.
8) Lewis AI, et al : Carotid-cavernous fistulas and intracavernous aneurysms. In : Neurosurgery, Vol. II (ed by Wilkins RH, Rengachary SS), p2529-2539, McGraw-Hill, New York, 1996.
9) Silverstein RL, et al : Activation of immobilized plasminogen by tissue activator. Multimolecular complex formation. J Biol Chem 260 : 10346-10352, 1985.
14) Shigekiyo T, et al : Congenital deficiency of histidine-rich glycoprotein : Failure to identify abnormalities in routine laboratory assays of hemostatic function, immunologic function, and traceelements. J Lab Clin Med 125 : 719-723, 1995.
15) Tsuchida-Straeten N, et al : Enhanced blood coagulation and fibrinolysis in mice lacking histidine-rich glycoprotein (HRG). J Thromb Haemostas 3 : 865-872, 2004.
P.578 掲載の参考文献
P.582 掲載の参考文献
1) 田中一郎ほか : 日本血栓止血学会後天性血友病 A診療ガイドライン. 血栓止血会誌 22 : 295-322, 2011.
3) 田中一郎ほか : わが国における後天性凝固因子インヒビターの実態に関する3年間の継続調査-予後因子に関する検討-. 血栓止血会誌 19 : 140-153, 2008.
4) 嶋緑倫 : 後天性凝固異常症の病態と治療 : 後天性血友病を中心に. 臨床血液 51 : 211-218, 2010.
9) Summner MJ, et al : Treatment of acquired haemophilia with recombinant activated FVII : a critical appraisal. Haemophilia 13 : 451-461, 2007.
P.586 掲載の参考文献
P.590 掲載の参考文献
4) 嶋緑倫 : 後天性凝固異常症の病態と治療 : 後天性血友病を中心に. 臨床血液 51 : 211-218, 2010.
10) Ichinose A, Souri M : Reduced difference of α2-plasmin inhibitor levels between plasma and serum in patients with severe factor XIII deficiency, including autoimmune hemorrhaphilia due to anti-factor XIII antibodies. Int J Hematol 95 : 47-50, 2012.
11) Miesbach W, et al : Rituximab in the treatment of factor XIII inhibitor possibly caused by Ciprofloxacin. Thromb Haemost 93 : 1001-1003, 2005.
P.598 掲載の参考文献
7) 日本血栓止血学会学術標準化委員会DIC部会 : 科学的根拠に基づいた感染症に伴うDIC治療のエキスパートコンセンサス. 日血栓止血会誌 20 (1) : 77-113, 2009.
8) Gando S, et al ; Japanese Association for Acute Medicine Disseminated Intravascular Coagulation (JAAM DIC) Study Group : A multicenter, prospective validation of disseminated intravascular coagulation diagnostic criteria for critically ill patients : comparing current criteria. Crit Care Med 34 (3) : 625-631, 2006.
14) Warren BL, et al ; KyberSept Trial Study Group : Caring for the critically ill patient. High-dose antithrombin III in severe sepsis : a randomized controlled trial. JAMA 286 (15) : 1869-1878, 2001.
16) Bernard GR, et al ; Recombinant human protein C Worldwide Evaluation in Severe Sepsis (PROWESS) study group : Efficacy and safety of recombinant human activated protein C for severe sepsis. N Engl J Med 344 (10) : 699-709, 2001.
P.604 掲載の参考文献
3) Lane A, Darmstadt GL : Kasabach-Merritt syndrome. In : Nelson Textbook of Pediatrics, 15th ed (ed by Behrman RE, et al), p1839, WB Saunders, Philadelphia, 1996.
6) Brizel HE, Raccuglia G : Giant hemangioma with thrombocytopenia. Radioisotopic demonstration of platelet sequestration. Blood 26 : 751-756, 1965.
7) Gilon E, et al : Multiple hemangiomata associated with thrombocytopenia : remarks on the pathogenesis of the thrombocytopenia in this syndrome. Blood 14 : 74-79, 1965.
8) Enjolras O, et al : Residual lesions after Kasabach-Merritt phenomenon in 41 patients. J Am Acad Dermatol 42 : 225-235, 2000.
13) Perez-Payarods J, et al : Treatment of life-threatening hemangiomas with vincristine. N Engl J Med 333 : 69, 1995.
P.607 掲載の参考文献
1) Acute Myeloid Leukemia with reccurent genetic abnormalities. In : WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, p112-114, International Agency for Research on Cancer (IARC), Lyon, 2008.
5) Falanga A, et al : Cancer procoagulant and tissue factor are differently modulated by all-trans-retinoic acid in acute promyelocytic leukemia cells. Blood 92 (1) : 143-151, 1998.
7) 日本血栓止血学会学術標準化委員会DIC部会 : 科学的根拠に基づいた感染症に伴うDIC治療のエキスパートコンセンサス. 日血栓止血会誌 20 (1) : 77-113, 2009.
P.611 掲載の参考文献
1) 白幡聡ほか : 新生児・乳児ビタミンK欠乏性出血症に対するビタミンK製剤投与の改訂ガイドライン (修正版). 日児誌 115 : 705-712, 2011.
4) 白幡聡ほか : 乳児ビタミンK欠乏性出血症全国調査成績 (1999~2004年). 日産婦新生児血会誌 16 : S55-56, 2006.
5) 板橋家頭夫 : ビタミンK欠乏性出血症予防のためのガイドライン. 周産期医学 41 : 1197-1201, 2011.
8) Williams MD, et al ; Haemostasis and Thrombosis Task Force, British Committee for Standards in Haematology : The investigation and management of neonatal haemostasis and thrombosis. Br J Haematol 119 : 295-309, 2002.
10) Chapter 10. Vitamin K. In : Human Vitamin and Mineral Requirements. Report of a joint FAO-WHO expert consultation (ed by Nantel G, Tontisirin K), p113-150, World Health Organization Food and Agriculture Organization of the United Nations, Rome, 2002.
11) National Academy of Science, Institute of Medicine, Food and Nutrition Board : Dietary Reference Intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc. Chapter 5, p12-196, National Academy Press, Washington, DC, 2001.
P.616 掲載の参考文献
1) Autret-Leca E, Jonville-Bera A : Vitamin K in neonates. Pediatr Drugs 3 : 1-8, 2001.
2) 白幡聡ほか : 新生児・乳児ビタミンK欠乏性出血症に対するビタミンK製剤投与の改訂ガイドライン (修正版). 日児誌 115 : 705-712, 2011.
3) Suttie JW : Vitamin K and human nutrition. J Am Diet Assoc 92 : 585-590, 1992.
5) 板橋家頭夫 : ビタミンK欠乏性出血症予防のためのガイドライン. 周産期医学 41 : 1197-1201, 2011.
8) 鈴木重統ほか : ジヘパプラスチンテストによる肝の異常と新生児期の肝成熟のスクリーニングに対する一考察. 北海道大学医療技術短期大学部紀要 5 : 1-9, 1992.
9) Kojima T, et al : Vitamin K concentrations in the maternal milk of Japanese women. Acta Paediatr 93 : 457-463, 2004.
10) Motohata K, et al : Relationship of milk intake and vitamin K supplementation to vitamin K status in newborns. Pediatrics 29 : 649-654, 1989.
P.618 掲載の参考文献
3) Reganon E, et al : Study of the formation of fibrin clot in cirrhotic patients. An approach to study of acquired dysfibrinogenemia. Thromb Res 46 (5) : 705-714, 1987.
11) Martinez J, et al : The role of sialic acid in the dysfibrinogenemi aassociated with liver disease : distribution of sialic acid on the constituent chains. Blood 61 (6) : 1196-1202, 1983.
P.623 掲載の参考文献
1) 毛利博 : 後天性von Willebrand症候群. 血小板血栓形成の分子機構 (関西血栓フォーラム編), p 106-116, 2002.
2) Federici AB, et a ; l Subcommittee on von Willebrand Factor : Acquired von Willebrand syndrome : data from an international registry. Thromb Haemost 84 : 345-349, 2000.
6) Mohri H, et al : Clinical significance of inhibitors in acquired von Willebrand syndrome. Blood 91 : 3623-3629, 1998.
11) Federici AB, et al : Treatment of acquired von Willebrand syndrome in patients with monoclonal gammopathy of uncertain significance : Comparison of three different therapeutic approaches. Blood 92 : 2707-2711, 1998.

最近チェックした商品履歴

Loading...