Idiopathic inflammatory myopathies: epidemiology, classification, and diagnostic criteria
Idiopathic inflammatory myopathies: epidemiology, classification, and diagnostic criteria
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DOI：
10.1016/s0889-857x(02)00021-2
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发表时间：
2002-11-01
影响因子：
2.3
通讯作者：
Phillips, BA
中科院分区：
文献类型：
--
作者：
Mastaglia, FL;Phillips, BA
特发性炎症性肌病 (IIM) 是一组异质性免疫介导的疾病，可能以孤立的形式存在，或与另一种自身免疫或结缔组织疾病、恶性肿瘤或罕见的感染或其他环境暴露相关。本文总结了 IIM 三种主要类型（皮肌炎、多发性肌炎和包涵体肌炎）流行病学方面的最新发现，并提出了这些疾病的分类和诊断标准方案。
The idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of immune-mediated disorders, that may present in an isolated form, or in association with another autoimmune or connective tissue disease, a malignancy, or, rarely, an infection or other environmental exposure. This article summarizes recent findings on epidemiologic aspects of the three major varieties of IIM (dermatomyositis, polymyositis and inclusion body myositis) and proposes schemes for the classification and diagnostic criteria for these conditions.