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美国急诊医学学会病例报告#22:多发性肌炎。

AAEM case report #22: polymyositis.

作者信息

Robinson L R

机构信息

Department of Rehabilitation Medicine, University of Washington School of Medicine, Seattle.

出版信息

Muscle Nerve. 1991 Apr;14(4):310-5. doi: 10.1002/mus.880140404.

Abstract

Polymyositis usually presents with progressive proximal muscle weakness, increased serum levels of muscle enzymes, inflammatory changes on muscle biopsy, and characteristic electromyographic (EMG) abnormalities. Motor unit action potential (MUAP) changes of configuration, duration, and amplitude are the most frequently observed EMG abnormality. Fibrillation potentials are commonly seen and tend to reflect active disease, diminishing after successful medical management or disease regression. Other muscle diseases can present with similar electromyographic abnormalities, thereby necessitating muscle biopsy for definitive diagnosis.

摘要

多发性肌炎通常表现为进行性近端肌无力、血清肌酶水平升高、肌肉活检有炎症改变以及特征性的肌电图(EMG)异常。运动单位动作电位(MUAP)在形态、时限和波幅方面的改变是最常观察到的EMG异常。纤颤电位很常见,往往反映疾病活动,在成功的药物治疗或疾病缓解后会减少。其他肌肉疾病也可能出现类似的肌电图异常,因此需要进行肌肉活检以明确诊断。

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