首页> 外文期刊>Der Hautarzt; Zeitschrift fuer Dermatologie, Venerologie, und verwandte Gebiete >[IgA pemphigus of the subcorneal pustular dermatosis type : Successful therapy with a combination of dapsone and acitretin].
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[IgA pemphigus of the subcorneal pustular dermatosis type : Successful therapy with a combination of dapsone and acitretin].

机译:角膜下脓疱性皮肤病类型IgA天疱疮:氨苯砜和阿维A联合治疗成功。

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摘要

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.
机译:角膜下脓疱性皮肤病类型的IgA天疱疮是一种在天疱疮频谱中罕见的自身免疫性水疱性疾病。患者的临床特征是广泛的红斑,主要影响三尖瓣区域。红斑性黄斑覆盖有许多囊泡和脓疱,偶有hypopyon形成。组织病理学表明,在水疱以及水肿的乳头状真皮中,裂口和许多嗜中性粒细胞裂开了。 IgA自身抗体在体内与表皮上半部的角质形成细胞结合。该疾病的自身抗原Desmocollin 1是桥粒钙黏着蛋白的成员,仅在分化程度更高的角质形成细胞上表达。在常规诊断中证明抗desmocollin 1的循环自身抗体具有挑战性,需要对desmocollin 1转染的COS7细胞进行间接免疫荧光染色。我们报告了一位病情较重的患者,仅对氨苯砜和阿维A酸的联合治疗有反应。

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