多发性肌炎/皮肌炎合并肺间质病变的中医病机探究  

Pathogenesis of Polymyositis or Dermatomyositis Combining with Interstitial Lung Disease

作　　者：王冉然[1] 张伟[2] 

机构地区：[1]山东中医药大学,山东济南250014 [2]山东中医药大学附属医院,山东济南250011

出　　处：《辽宁中医杂志》2016年第8期1617-1618,共2页Liaoning Journal of Traditional Chinese Medicine

基　　金："泰山学者"建设工程专项经费资助项目(ts20110819)

摘　　要：特发性炎症性肌病是一种以侵犯骨骼肌为主的系统性自身免疫病,可以累及全身,常常并发肺间质性改变,预后往往不佳。文章试从中医的角度探寻多发性肌炎/皮肌炎合并肺间质病变的发病机制与临床特点,并为临床治疗提供思路。The idiopathic inflammatory myopathies is a systemic autoimmune disease whose major characteristic is invading the skeletal muscle. It intends to involve the whole body with interstitial lung disease and it is very hard to be cured. This article tries to research the pathogenesis and clinical characteristics of the IIM and PM combining with the ILD and puts forward a method about remedy.

关 键 词：多发性肌炎/皮肌炎 肺间质病变 中医 病机 治法 

分 类 号：R593.26[医药卫生—内科学]