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急性特发性多神经炎中主要的上肢无力:一种独特的区域变异型。

Predominant arm weakness in acute idiopathic polyneuritis: a distinct regional variant.

作者信息

Busby M, Donaghy M

机构信息

University Department of Clinical Neurology, Radcliffe Infirmary, Oxford, UK.

出版信息

J Neurol. 2000 May;247(5):343-5. doi: 10.1007/s004150050600.

Abstract

Acute idiopathic polyneuritis is a heterogeneous disorder with a number of clearly established variants. We describe four patients who present with an acute neuropathy predominantly affecting the arms which we believe should be considered as a distinct variant of acute polyneuritis. In two cases a primary demyelinating process affecting both motor and sensory nerves is suggested whereas in the other two the features were of a pure motor axonal degeneration. The relationship between these neuropathies, other variants of acute idiopathic polyneuritis and multifocal motor neuropathy is considered.

摘要

急性特发性多神经炎是一种具有多种明确变体的异质性疾病。我们描述了4例主要累及上肢的急性神经病变患者,我们认为应将其视为急性多神经炎的一种独特变体。在2例中,提示存在影响运动和感觉神经的原发性脱髓鞘过程,而在另外2例中,特征为单纯运动性轴索性变性。我们还探讨了这些神经病变、急性特发性多神经炎的其他变体以及多灶性运动神经病之间的关系。

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