Wenzel J, Uerlich M, Gerdsen R, Bieber T, Boehm I
Department of Dermatology, University of Bonn, Germany.
Rheumatol Int. 2001 Oct;21(2):75-7. doi: 10.1007/s002960100137.
We present the case of a 71-year-old man with inclusion body myositis combined with subacute cutaneous lupus erythematosus and dysphagia. Although inclusion body myositis is usually resistant to immunosuppressive therapy, this patient improved under treatment with corticosteroids. The presented case is discussed in the context of earlier reports of inclusion body myositis and lupus erythematosus.
我们报告一例71岁男性患者，患有包涵体肌炎合并亚急性皮肤型红斑狼疮及吞咽困难。尽管包涵体肌炎通常对免疫抑制治疗耐药，但该患者在皮质类固醇治疗下病情有所改善。本文结合既往包涵体肌炎和红斑狼疮的报告对该病例进行讨论。
