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吉兰-巴雷综合征的急性轴索性形式。

An acute axonal form of Guillain-Barré polyneuropathy.

作者信息

Feasby T E, Gilbert J J, Brown W F, Bolton C F, Hahn A F, Koopman W F, Zochodne D W

出版信息

Brain. 1986 Dec;109 ( Pt 6):1115-26. doi: 10.1093/brain/109.6.1115.

Abstract

Five patients with a clinical diagnosis of acute Guillain-Barré polyneuropathy (GBP) had electrically inexcitable motor nerves. All were quadriplegic. One patient died and 3 of the 4 survivors showed poor recovery. Autopsy studies on the patient who died showed severe axonal degeneration in nerve roots and distal nerves without inflammation or demyelination. Electrophysiological studies in these patients suggested that the predominant process was axonal degeneration. These cases may represent a separate clinicopathological entity, and constitute a variant of GBP characterized by an acute axonal neuropathy.

摘要

5例临床诊断为急性吉兰-巴雷综合征(GBP)的患者,其运动神经电刺激无反应。所有患者均为四肢瘫痪。1例患者死亡,4例幸存者中有3例恢复不佳。对死亡患者的尸检研究显示神经根和远端神经有严重的轴突变性,无炎症或脱髓鞘表现。这些患者的电生理研究提示主要病变过程是轴突变性。这些病例可能代表一种独立的临床病理实体,构成以急性轴索性神经病为特征的GBP变异型。

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