Jablecki C
Muscle Nerve. 1984 Mar-Apr;7(3):250-7. doi: 10.1002/mus.880070311.
This review of the Lambert-Eaton myasthenic syndrome (LEMS) emphasizes electrodiagnosis and includes a case report. A 50-year-old woman had become progressively weaker over 1.5 years. The suspected diagnosis was confirmed by the clinical electrophysiological findings and was made 6 months before the patient's oat-cell carcinoma was found. After treating with local radiation and chemotherapy, the myasthenic syndrome went into remission as the pulmonary lesion resolved.
这篇关于兰伯特-伊顿肌无力综合征（LEMS）的综述着重于电诊断，并包含一例病例报告。一名50岁女性在1.5年里逐渐变得虚弱。临床电生理检查结果证实了疑似诊断，且该诊断在患者燕麦细胞癌被发现前6个月就已做出。在接受局部放疗和化疗后，随着肺部病变的消退，肌无力综合征进入缓解期。
