White S W, Tesar J T
Arch Dermatol. 1982 Aug;118(8):599-601.
Primary hypothyroidism, dermatomyositis, dermatitis herpetiformis (DH), and Sjögren's syndrome developed sequentially, over a 20-year period, in a 67-year-old woman. The principal manifestations of her illness were periodic and simultaneous exacerbations of dermatomyositis and DH. Her histocompatability antigens were A1,B8, a haplotype associated with autoimmune diseases. We suggest that this unusual disease complex has a genetic basis.
一名67岁女性在20年期间先后出现原发性甲状腺功能减退、皮肌炎、疱疹样皮炎(DH)和干燥综合征。她疾病的主要表现是皮肌炎和DH周期性同时加重。她的组织相容性抗原为A1、B8,这是一种与自身免疫性疾病相关的单倍型。我们认为这种不寻常的疾病复合体有遗传基础。