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特殊型天疱疮、重症肌无力与恶性胸腺瘤并存。

Coexistence of peculiar pemphigus, myasthenia gravis and malignant thymoma.

作者信息

Tagami H, Imamura S, Noguchi S, Nishitani H

出版信息

Dermatologica. 1976;152(3):181-90. doi: 10.1159/000251246.

Abstract

An unusual vesculobullous disease and myasthenia gravis occurred concurrently with a malignant thymoma in a Japanese male. The bullous dermatosis had combined clinical and histological features of both dermatitis herpetiformis and pemphigus. Serum showed striated muscle antibodies and intercellular epithelial autoantibodies; the latter had been demonstrated even prior to the development of the skin lesions. Thus, immunologically, this dermatosis was confirmed to be a variety of pemphigus.

摘要

一名日本男性同时出现了一种罕见的血管性大疱病、重症肌无力和恶性胸腺瘤。这种大疱性皮肤病具有疱疹样皮炎和天疱疮的临床及组织学特征。血清显示有横纹肌抗体和细胞间上皮自身抗体;后者甚至在皮肤病变出现之前就已被证实存在。因此,从免疫学角度来看,这种皮肤病被确认为一种天疱疮。

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