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儿童“假”性肥大性神经病

"Pseudo" hypertrophic neuropathy of childhood.

作者信息

Baba M, Takada H, Miura H, Okushima T, Matsunaga M

机构信息

Department of Neurology, Hirosaki University School of Medicine, Japan.

出版信息

J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):236-7. doi: 10.1136/jnnp.58.2.236.

Abstract

A 9 year old boy had chronic progressive motor-sensory neuropathy that started in early infancy. He had enlarged nerves and pes cavus deformity. Motor conduction studies showed very dispersed, polyphasic compound muscle action potentials with conduction velocities around 2 m/s. A sural nerve biopsy showed severe loss of myelinated fibres. Two months of treatment with corticosteroids restored muscle power. During this time the enlarged nerves became normal and electrophysiological recovery was achieved. Chronically acquired neuropathy in infancy is strikingly similar to genetically determined neuropathy.

摘要

一名9岁男孩自婴儿早期起就患有慢性进行性运动感觉神经病。他有神经粗大和高弓足畸形。运动传导研究显示复合肌肉动作电位非常离散、多相,传导速度约为2米/秒。腓肠神经活检显示有髓纤维严重丧失。使用皮质类固醇治疗两个月后肌肉力量恢复。在此期间,粗大的神经恢复正常,实现了电生理恢复。婴儿期慢性获得性神经病与基因决定的神经病极为相似。

相似文献

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"Pseudo" hypertrophic neuropathy of childhood.儿童“假”性肥大性神经病
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