Tagami H, Imamura S, Noguchi S, Nishitani H
Dermatologica. 1976;152(3):181-90. doi: 10.1159/000251246.
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.
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。
