大疱性类天疱疮
自身抗体
银屑病
类天疱疮
瘢痕性类天疱疮
抗体
医学
红斑
组织病理学
寻常性天疱疮
层粘连蛋白
病理
皮肤病科
免疫学
自身免疫性疾病
化学
生物化学
细胞
作者
Akiko Imanishi,Chiharu Tateishi,Hisayoshi Imanishi,Junko Sowa‐Osako,Hiroshi Koga,Daisuke Tsuruta,Takashi Hashimoto
标识
DOI:10.1111/1346-8138.12798
摘要
Abstract Both anti‐laminin γ1 pemphigoid and bullous pemphigoid are autoimmune subepidermal blistering diseases. The former is rare and characterized by autoantibodies to laminin γ1, a 200‐kDa dermal protein, while the latter is common among the elderly and characterized by autoantibodies to BP 180 and BP 230, both of which are hemidesmosomal proteins. We experienced a 69‐year‐old Japanese male patient with blister formation secondary to erythrodermic psoriasis, which was successfully treated with cyclosporin. The histopathology of erythema corresponded with psoriasis and that of a blistering lesion showed infiltration of neutrophils and eosinophils in and around the subepidermal blisters. Patient immunoglobulin G antibodies labeled both the epidermal and dermal sides of 1 mol/L NaCl‐split human skin by indirect immunofluorescent microscopy and recognized laminin γ1, BP 180 and BP 230 by immunoblotting. To the best of our knowledge, this is the first report of coexistence of psoriasis and atypical pemphigoid with these three autoantibodies.
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