多发性肌炎、皮肌炎和自身免疫性坏死性肌病：临床特征。
Polymyositis, dermatomyositis, and autoimmune necrotizing myopathy: clinical features.
机构信息
Division of Rheumatology, Department of Medicine, Johns Hopkins University School of Medicine, 5200 Eastern Avenue, Mason F. Lord Center Tower, Suite 4100, Baltimore, MD 21224, USA.
出版信息
Rheum Dis Clin North Am. 2011 May;37(2):143-58, v. doi: 10.1016/j.rdc.2011.01.001.
Idiopathic inflammatory myopathies are a heterogeneous group of autoimmune disorders predominantly affecting skeletal muscles, resulting in muscle inflammation and weakness. The 3 most common inflammatory myopathies are polymyositis (PM), dermatomyositis (DM), and inclusion body myositis. This review details the clinical findings noted in PM, DM, and the emerging entity of autoimmune necrotizing myopathy.
特发性炎性肌病是一组异质性自身免疫性疾病，主要累及骨骼肌，导致肌肉炎症和无力。3 种最常见的炎性肌病是多发性肌炎（PM）、皮肌炎（DM）和包涵体肌炎。本文详细介绍了 PM、DM 和新出现的自身免疫性坏死性肌病的临床发现。
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