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在West综合征中进行胼胝体切开术提示高峰节律紊乱的皮质起源。

Callosotomy in West syndrome suggests a cortical origin of hypsarrhythmia.

作者信息

Pinard J M, Delalande O, Plouin P, Dulac O

机构信息

Service de Neuropédiatrie, Hôpital Saint Vincent de Paul, Paris, France.

出版信息

Epilepsia. 1993 Jul-Aug;34(4):780-7. doi: 10.1111/j.1528-1157.1993.tb00461.x.

Abstract

Hypsarrhythmia and spasms of West syndrome have been postulated by some investigators to have a brainstem origin. Cortical involvement is also postulated because of the frequent association with cortical lesions. Cortical discharges have been proposed to stimulate subcortical structures (i.e., brainstem) and hypsarrhythmia is a secondarily generalized phenomenon produced by the brainstem. Two children with cryptogenic West syndrome refractory for several years to steroids and conventional antiepileptic drugs underwent total callosotomy. Hypsarrhythmia that was bilateral before operation became unilateral after the procedure and spasms became asymmetrical, suggesting that a corticocortical pathway through the corpus callosum is important in the generalization of hypsarrhythmia.

摘要

一些研究者推测,婴儿痉挛症和韦斯特综合征的痉挛起源于脑干。由于常与皮质病变相关,也推测有皮质受累。有人提出皮质放电会刺激皮质下结构(即脑干),婴儿痉挛症是由脑干产生的继发性全身性现象。两名患有隐源性韦斯特综合征的儿童,多年来对类固醇和传统抗癫痫药物难治,接受了胼胝体全切开术。术前双侧的婴儿痉挛症术后变为单侧,痉挛也变得不对称,这表明通过胼胝体的皮质-皮质通路在婴儿痉挛症的泛化中起重要作用。

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