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伊顿-兰伯特肌无力综合征:两例具有典型和非典型特征的病例。

Eaton-Lambert myasthenic syndrome: two cases with typical and atypical features.

作者信息

Anderson T J, Carroll G J, Avery S F, Donaldson I M, Parkin P J

机构信息

Department of Neurology, Christchurch Hospital.

出版信息

N Z Med J. 1990 May 23;103(890):240-2.

PMID:2160629
Abstract

Eaton-Lambert myasthenic syndrome is a rare disorder of neuromuscular transmission. We are unaware of previous New Zealand reports and present two patients. Characteristic abnormalities in compound muscle action potential amplitude following repetitive nerve stimulation and on single fibre electromyography were present. Both patients also showed mild patchy abnormalities in peripheral nerve conduction. The clinical picture resembled Guillain-Barre syndrome in one patient who developed severe generalised weakness and respiratory failure. In both patients the neurological presentation lead to the recognition of a previously asymptomatic small cell lung carcinoma.

摘要

伊顿-兰伯特肌无力综合征是一种罕见的神经肌肉传递障碍性疾病。我们未发现此前有新西兰的相关报道,现报告两例患者。患者在重复神经刺激后复合肌肉动作电位幅度及单纤维肌电图检查存在特征性异常。两名患者周围神经传导也均有轻度散在异常。其中一名患者出现严重的全身无力和呼吸衰竭,其临床表现类似吉兰-巴雷综合征。两名患者的神经学表现均提示此前无症状的小细胞肺癌。

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