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一名感染人类免疫缺陷病毒(HIV)的患者出现兰伯特-伊顿肌无力综合征的轻度临床表现。

Mild clinical expression of Lambert-Eaton myasthenic syndrome in a patient with HIV infection.

作者信息

Truffert Andre, Allali Gilles, Vokatch Natalia, Lalive Patrice H

机构信息

University Hospital of Geneva, Micheli-du-Crest 24, Geneva 14, 1211, Switzerland.

出版信息

BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.08.2008.0649. Epub 2009 Jan 23.

DOI:10.1136/bcr.08.2008.0649
PMID:21686701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3028063/
Abstract

Neuromuscular complications of HIV are related to immunodeficiency, direct cytotoxicity of the virus or side effect of the treatments. Autoimmune disorders involving the nervous system, including Guillain-Barre syndrome, myositis and vasculitis, have been described in association with HIV. Neuromuscular junction autoimmune diseases such as myasthenia gravis have been occasionally reported in patients with HIV, whereas the Lambert-Eaton myasthenic syndrome (LEMS) has never been described. We report an unusual case of paucisymptomatic LEMS in a patient with HIV infection.

摘要

HIV的神经肌肉并发症与免疫缺陷、病毒的直接细胞毒性或治疗的副作用有关。涉及神经系统的自身免疫性疾病,包括格林-巴利综合征、肌炎和血管炎,已被描述与HIV相关。神经肌肉接头自身免疫性疾病,如重症肌无力,在HIV患者中偶尔有报道,而兰伯特-伊顿肌无力综合征(LEMS)从未被描述过。我们报告了一例HIV感染患者出现症状轻微的LEMS罕见病例。

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BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.08.2008.0649. Epub 2009 Jan 23.
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Lambert-Eaton myasthenic syndrome (LEMS): a rare autoimmune presynaptic disorder often associated with cancer. Lambert-Eaton 肌无力综合征(LEMS):一种罕见的自身免疫性突触前疾病,常与癌症相关。
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本文引用的文献

1
Lambert-Eaton myasthenic syndrome.兰伯特-伊顿肌无力综合征
Rev Neurol (Paris). 2004 Feb;160(2):177-80. doi: 10.1016/s0035-3787(04)70888-7.
2
The neurology of HIV infection.HIV感染的神经学
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3
HIV and autoimmunity.艾滋病病毒与自身免疫
Autoimmun Rev. 2002 Dec;1(6):329-37. doi: 10.1016/s1568-9972(02)00086-1.
4
An improved diagnostic assay for Lambert-Eaton myasthenic syndrome.一种用于兰伯特-伊顿肌无力综合征的改进诊断检测方法。
J Neurol Neurosurg Psychiatry. 1995 Jan;58(1):85-7. doi: 10.1136/jnnp.58.1.85.
5
Transient myasthenia gravis during HIV infection.HIV感染期间的短暂性重症肌无力
Muscle Nerve. 1995 Aug;18(8):914-6. doi: 10.1002/mus.880180819.