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伴有近端上肢受累的良性单肢肌萎缩:病例报告

Benign monomelic amyotrophy with proximal upper limb involvement: case report.

作者信息

Neves Marco Antonio Orsini, Freitas Marcos R G de, Mello Mariana Pimentel de, Dumard Carlos Henrique, Freitas Gabriel R de, Nascimento Osvaldo J M

机构信息

Clinical Neurology - UNIFESO - Fundação Educacional Serra dos Orgãos (Teresópolis) and Department of Neurology (Neuromuscular Diseases Division) - UFF.

出版信息

Arq Neuropsiquiatr. 2007 Jun;65(2B):524-7. doi: 10.1590/s0004-282x2007000300032.

Abstract

Monomelic amyotrophy (MA) is a rare condition in which neurogenic amyotrophy is restricted to an upper or lower limb. Usually sporadic, it usually has an insidious onset with a mean evolution of 2 to 4 years following first clinical manifestations, which is, in turned, followed by stabilization. We report a case of 20-years-old man who presented slowly progressive amyotrophy associated with proximal paresis of the right upper limb, which was followed by clinical stabilization 4 years later. Eletroneuromyography revealed denervation along with myofasciculations in various muscle groups of the right upper limb. We call attention to this rare location of MA, as well as describe some theories concerning its pathophysiology .

摘要

单肢肌萎缩(MA)是一种罕见病症,其中神经源性肌萎缩局限于上肢或下肢。通常为散发性,起病隐匿,首次出现临床表现后平均病程为2至4年,随后病情稳定。我们报告一例20岁男性病例,该患者出现与右上肢近端轻瘫相关的缓慢进行性肌萎缩,4年后病情临床稳定。肌电图显示右上肢不同肌肉群存在去神经支配以及肌束震颤。我们提请注意MA这种罕见的发病部位,并描述一些关于其病理生理学的理论。

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