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临床及电诊断方面的纯感觉性脱髓鞘性多发性神经病。

Clinically and electrodiagnostically pure sensory demyelinating polyneuropathy.

作者信息

Rubin M, Mackenzie C R

机构信息

Department of Neurology, Hospital for Special Surgery, New York, NY, USA.

出版信息

Electromyogr Clin Neurophysiol. 1996 Apr-May;36(3):145-9.

PMID:8737935
Abstract

A 35-year-old woman presented with a 4 year history of stepwise sensory loss which progressed in an asymmetrical fashion (mononeuropathy multiplex) and developed into a relatively symmetric polyneuropathy which was purely sensory by clinical and electrodiagnostic criteria. Sural nerve biopsy revealed demyelination with axonal sparing. Extensive laboratory evaluation failed to reveal a definite cause. This case is unique among well-documented cases of chronic inflammatory demyelinating polyneuropathy (CIDP) in that it is purely sensory by both clinical and electrodiagnostic criteria, and may represent a distinct entity rather than an extension of the spectrum of CIDP.

摘要

一名35岁女性,有4年逐步进展的感觉丧失病史,呈不对称性进展(多灶性单神经病),并发展为相对对称的多发性神经病,根据临床和电诊断标准,该多发性神经病为纯感觉性。腓肠神经活检显示脱髓鞘且轴突保留。广泛的实验室检查未能发现明确病因。在已充分记录的慢性炎症性脱髓鞘性多发性神经病(CIDP)病例中,该病例具有独特性,因为根据临床和电诊断标准,它均为纯感觉性,可能代表一种独特的疾病实体,而非CIDP谱系的延伸。

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