可能的重症肌无力和lems在同一患者:病例报告和文献复习

V. Patel, P. Bill, A. Bhigjee
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引用次数: 3

摘要

重症肌无力(MG)合并Lambert-Eaton肌无力综合征(LEMS)在同一患者中很少被描述。这是一个病例报告,患者最初表现为重症肌无力,后来可能并发自身免疫性LEMS。这个病人被发现是HIV阳性。兴趣在于免疫功能低下患者的MG行为以及MG和LEMS患者神经肌肉连接处的电生理变化。我们提出一个病人谁是HIV阳性与长期历史的MG和一个可能是最近诊断LEMS。朗伯-伊顿肌无力综合征协会是一项患者治疗计划。目前的研究结果显示,患者、hiv阳性、患者的初始症状、肌无力症状、患者的完全免疫系统、患者的初始自身免疫系统、患者的最终症状、患者的致病机制均不确定。关键词:重症肌无力,Lambert-Eaton症型,HIV,重症肌无力,Lambert-Eaton症型,病毒免疫缺陷获得性,VIH非洲神经科学Vol.23(2) 2004
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POSSIBLE MYASTHENIA AND LEMS IN THE SAME PATIENT :CASE REPORT AND REVIEW OF THE LITERATURE
ABSTRACT Myasthenia gravis (MG) together with Lambert-Eaton myasthenic syndrome (LEMS) in the same patient is rarely described. This is a case report of a patient who initially presented with myasthenia gravis and later complicated with presumably auto-immune LEMS. The patient was noted to be HIV positive. The interest lies in the behaviour of MG in immunocompromised patients and the electrophysiological changes at the neuromuscular junction in patients with both MG and LEMS. We present a patient who is HIV positive with a long history of MG and a possibly a more recent diagnosis of LEMS. RESUME L'association myasthenie et syndrome de Lambert-Eaton chez un patient est rarement decrit. Nous rapportons le cas d'un patient, VIH positif, s'etant presente initialement par une myasthenie, completee ulterieurement par un syndrome de Lambert Eaton vraisemblablement d'origine auto-immune et discutons les liens eventuels, au plan pathogenique. Key words : Myasthenia Gravis, Lambert Eaton myasthenic syndrome, HIV, Myasthenie, syndrome de Lambert-Eaton, virus d'immunodeficience acquise, VIH African Journal of Neurological Sciences Vol.23(2) 2004
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