A case of acquired haemophilia A in a patient with bullous pemphigoid and review of the Japanese literature

被引：7

作者：

Chijiwa, Chika ^{[1
]}

Kamata, Masahiro ^{[1
]}

Fukuyasu, Atsuko ^{[1
]}

Shono, Yuki ^{[1
]}

Takeoka, Shintaro ^{[1
]}

Tateishi, Mihoko ^{[1
]}

Fukaya, Saki ^{[1
]}

Hayashi, Kotaro ^{[1
]}

Tanaka, Takamitsu ^{[1
]}

Ishikawa, Takeko ^{[1
]}

Ohnishi, Takamitsu ^{[1
]}

Saito, Koji ^{[2
]}

Ishii, Norito ^{[3
]}

Hashimoto, Takashi ^{[4
]}

Tada, Yayoi ^{[1
]}

机构：

[1] Teikyo Univ, Sch Med, Dept Dermatol, Tokyo, Japan

[2] Teikyo Univ, Sch Med, Dept Pathol, Tokyo, Japan

[3] Kurume Univ, Sch Med, Dept Dermatol, Fukuoka, Fukuoka, Japan

[4] Kurume Univ, Sch Med, Inst Cutaneous Cell Biol, Fukuoka, Fukuoka, Japan

来源：

EUROPEAN JOURNAL OF DERMATOLOGY | 2018年 / 28卷 / 03期

关键词：

BLISTER FORMATION; IGG4; COMPLEMENT; DOMAIN;

D O I：

10.1684/ejd.2018.3284

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

引用

页码：422 / 423

页数：3

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[6]

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[7] Autoantibodies to the extracellular and intracellular domain of bullous pemphigoid 180, the putative key autoantigen in bullous pemphigoid, belong predominantly to the TgG1 and IgG4 subclasses [J].

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[8] The predominance of IgG4 in prodromal bullous pemphigoid [J].

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[9] Anti-factor VIII IgA as a potential marker of poor prognosis in acquired hemophilia A: results from the GTH-AH 01/2010 study [J].

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