1) 五十嵐徹, 高山良子 : IgA血管炎. 小児リウマチ学. 南山堂, 2021 : 189-192.
2) 川名誠司 : IgA血管炎. 川名誠司, 陳科榮 (編), 皮膚血管炎. 第2版, 医学書院, 2022 : 145-163.
3) Jennette JC, Falk RJ, Andrassy K, et al. : Nomenclature of systemic vasculitides. Proposal of an international consensus conference. Arthritis Rheum 1994 ; 37 : 187-192.
4) Mills JA, Michel BA, Bloch DA, et al. : The American College of Rheumatology 1990 criteria for the classification of Henoch-Schonlein purpura. Arthritis Rheum 1990 ; 33 : 1114-1121.
5) Ozen S, Ruperto N, Dillon MJ, et al. : EULAR/PReS endorsed consensus criteria for the classification childhood vasculitis, Ann Rheum Dis 2006 ; 65 : 936-941.
6) Ozen S, Pistorio A, Iusan SM, et al. : EULAR/PRINTO/PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis : Ankara 2008. Part II : Final classification criteria. Ann Rheum Dis 2010 ; 69 : 798-806.
7) Jennette JC, Falk RJ, Bacon PA, et al. : 2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitis. Arthritis Rheum 2013 ; 65 : 1-11.
8) 日本循環器学会, 他 : 血管炎症候群の診療ガイドライン (2017年改訂版). 2018 : 78-83 (https://www.j-circ.or.jp/cms/wp-content/uploads/2020/02/JCS2017_isobe_h.pdf) (参照 2022-5-20)
9) 日本皮膚科学血管炎・血管障害診療ガイドライン改訂版作成委員会 : 血管炎・血管障害診療ガイドライン 2016年改訂版. 日皮会誌 2017 ; 127 : 299-415.
10) Kawana S, Ohta M, Nishiyama S : Value of the assay for IgA-containing circulating immune complexes in Henoch-Schonlein purpura. Dermatologia 1986 ; 172 : 245-253.
11) Narimatsu Y, Kubota T, Furukawa S, et al. : Effect of glycosylation on cis/trans isomerization of prolines in IgA1-hinge peptide. J Am Chem Soc 2010 ; 132 : 5548-5549.
12) Suzuki H, Yasutake J, Makita Y, et al. : IgA nephropathy and IgA vasculitis with nephritis have a shared feature involving galactose-deficient IgA1-oriented pathogenesis. Kid Int 2018 ; 93 : 700-705.
13) 矢田純一 (著) : III型アレルギー. 医系免疫学改訂 16版. 中外医学社, 2021 : 813-816.
14) Heineke MH, Ballering AV, Jamin A, et al. : New insights in the pathogenesis of immunoglobulin A vasculitis (Henoch-Schonlein purpura). Autoimmun Rev 2017 ; 16 : 1246-1253.