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[角层下脓疱性皮病型IgA天疱疮。氨苯砜和阿维A联合治疗成功]

[IgA pemphigus of the subcorneal pustular dermatosis type. Successful therapy with a combination of dapsone and acitretin].

作者信息

Monshi B, Richter L, Hashimoto T, Groiß E, Haensch N, Rappersberger K

机构信息

Abteilung für Dermatologie und Venerologie, Krankenanstalt Rudolfstiftung, Juchgasse 25, 1030, Wien, Österreich.

出版信息

Hautarzt. 2012 Jun;63(6):482-6. doi: 10.1007/s00105-011-2270-2.

Abstract

IgA pemphigus of the subcorneal pustular dermatosis type is a rare autoimmune blistering disease in the pemphigus spectrum. Patients are clinically characterized by extensive erythemas that primarily affect intertriginous areas. The erythematous macules are covered with numerous vesicles and pustules with occasional hypopyon formation. Histopathology shows subcorneal acantholysis with clefting and numerous neutrophils within the blister as well as in the edematous papillary dermis. IgA autoantibodies bind in vivo to keratinocytes within the upper half of the epidermis. Desmocollin 1, the autoantigen of this disease, is a member of desmosomal cadherins and is only expressed on more differentiated keratinocytes. The demonstration of circulating autoantibodies against desmocollin 1 in routine diagnosis is challenging and requires indirect immunofluorescence staining of desmocollin 1 transfected COS7 cells. We report a patient with a severe course of the disease who only responded to combined therapy with dapsone and acitretin.

摘要

角层下脓疱性皮病型IgA天疱疮是天疱疮谱系中一种罕见的自身免疫性水疱病。患者的临床特征为广泛的红斑,主要累及皮肤褶皱部位。红斑性斑疹上覆盖着大量水疱和脓疱,偶尔形成积脓。组织病理学显示角层下棘层松解,水疱内以及水肿的乳头真皮层有裂隙和大量中性粒细胞。IgA自身抗体在体内与表皮上半部分的角质形成细胞结合。该疾病的自身抗原桥粒芯糖蛋白1是桥粒钙黏蛋白的成员,仅在分化程度较高的角质形成细胞上表达。在常规诊断中检测循环抗桥粒芯糖蛋白1自身抗体具有挑战性,需要对转染桥粒芯糖蛋白1的COS7细胞进行间接免疫荧光染色。我们报告了一名病情严重的患者,其仅对氨苯砜和阿维A联合治疗有反应。

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