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韦斯特综合征行胼胝体切开术后双侧独立癫痫性痉挛的发生情况

Occurrence of bilaterally independent epileptic spasms after a corpus callosotomy in West syndrome.

作者信息

Kobayashi Katsuhiro, Endoh Fumika, Toda Yoshihiro, Oka Makio, Baba Hiroshi, Ohtsuka Yoko, Yoshinaga Harumi

机构信息

Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences and Okayama University Hospital, Shikatacho 2-chome 5-1, Kita-ku, Okayama, Japan.

Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences and Okayama University Hospital, Shikatacho 2-chome 5-1, Kita-ku, Okayama, Japan.

出版信息

Brain Dev. 2016 Jan;38(1):132-5. doi: 10.1016/j.braindev.2015.05.003. Epub 2015 May 18.

Abstract

We report a patient with intractable West syndrome whose epileptic spasms (ESs) were initially bilaterally synchronous, as is typical; after a complete corpus callosotomy, however, bilaterally independent ESs originated in either hemisphere. Activity of probable cortical origin associated with ESs was detected by observing ictal gamma oscillations. Brain MRI revealed no structural abnormality before surgery. This case suggests that ESs with a hemispheric origin may appear generalized because of synchronizing effects in the corpus callosum in some patients.

摘要

我们报告了一名患有难治性韦斯特综合征的患者,其癫痫痉挛(ESs)最初如典型情况一样是双侧同步的;然而,在进行完全胼胝体切开术后,双侧独立的ESs起源于任一脑半球。通过观察发作期伽马振荡检测到了与ESs相关的可能源于皮质的活动。术前脑部MRI未显示结构异常。该病例表明,在一些患者中,由于胼胝体的同步作用,起源于半球的ESs可能表现为全身性。

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