Exploring Road of Classification Criteria for Idiopathic Inflammatory Myopathy  

作　　者：Yu-Hui Li Guo-Chun Wang Zhan-Guo Li 

机构地区：[1]Department of Rheumatology and Immunology,Peking University People's Hospital,Beijing 100044,China [2]Department of Rheumatology and Immunology,China-Japan Friendship Hospital,Beijing,China

出　　处：《Chinese Medical Journal》2018年第23期2773-2775,共3页中华医学杂志（英文版）

摘　　要：Idiopathic inflammatory myopathies (IIMs) are heterogeneous disorders characterized by chronic muscle weakness and muscle fatigue and mononuclear cell infiltration into skeletal muscle.[1] The most common subgroups in adults are dermatomyositis (DM), polymyositis (PM), amyopathic DM (ADM), inclusion body myositis (IBM), and juvenile DM (JDM). Several diagnostic or classification criteria for IIM have been developed.[2?5] Classification criteria are mostly used in research and clinical trials, not daily in practice. Great efforts have been dedicated in pursuing new criteria in the past decades.

关 键 词：AUTOIMMUNE DISEASES CRITERIA DERMATOMYOSITIS POLYMYOSITIS 

分 类 号：R[医药卫生]