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肌无力模式、运动神经元病的分类以及散发性肌萎缩侧索硬化症的临床诊断

Patterns of Weakness, Classification of Motor Neuron Disease, and Clinical Diagnosis of Sporadic Amyotrophic Lateral Sclerosis.

作者信息

Statland Jeffrey M, Barohn Richard J, McVey April L, Katz Jonathan S, Dimachkie Mazen M

机构信息

Department of Neurology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Mailstop 2012, Kansas City, KS 66160, USA.

Department of Neurology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Mailstop 2012, Kansas City, KS 66160, USA.

出版信息

Neurol Clin. 2015 Nov;33(4):735-48. doi: 10.1016/j.ncl.2015.07.006. Epub 2015 Sep 8.

Abstract

When approaching a patient with suspected motor neuron disease (MND), the pattern of weakness on examination helps distinguish MND from other diseases of peripheral nerves, the neuromuscular junction, or muscle. MND is a clinical diagnosis supported by findings on electrodiagnostic testing. MNDs exist on a spectrum, from a pure lower motor neuron to mixed upper and lower motor neuron to a pure upper motor neuron variant. Amyotrophic lateral sclerosis (ALS) is a progressive mixed upper and lower motor neuron disorder, most commonly sporadic, which is invariably fatal. This article describes a pattern approach to identifying MND and clinical features of sporadic ALS.

摘要

在接诊疑似运动神经元病(MND)的患者时,检查发现的肌无力模式有助于将MND与其他周围神经、神经肌肉接头或肌肉疾病相鉴别。MND是一种基于电诊断测试结果支持的临床诊断。MND存在一个谱系,从单纯的下运动神经元型到上下运动神经元混合型,再到单纯的上运动神经元型。肌萎缩侧索硬化症(ALS)是一种进行性的上下运动神经元混合型疾病,最常见为散发性,且必然致命。本文介绍了一种识别MND的模式方法以及散发性ALS的临床特征。

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