特发性炎性肌病骨骼肌功能异常的发生机制
摘要
特发性炎性肌病（idiopathic inflammatory myositis，IIM）是一组以进行性对称性近端肌无力为主要特点，可伴有发热、关节痛、吞咽困难、肺间质病变、心肾受累等表现的临床综合征，临床以多发性肌炎（polymyositis）和皮肌炎（dermatomyosi．tis）最常见。IIM的肌肉病理改变并不全相同，其肌无力的发生、发展和转归机制目前并不十分清楚。多发性肌炎，皮肌炎最常累及的肌肉群依次为髋屈肌、髋伸肌、髋外展肌、颈屈肌、肩外展肌，多发性肌炎肌无力的程度常常重于皮肌炎。
出处
《中华风湿病学杂志》
CAS
CSCD
北大核心
2013年第6期418-420,共3页
Chinese Journal of Rheumatology
基金
国家自然科学基金（81072457）
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