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腹型癫痫相关皮质肌阵挛的独特 EEG 标志物。

A Distinct EEG Marker of Celiac Disease-Related Cortical Myoclonus.

机构信息

Edmond J. Safra Program in Parkinson's Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital and Division of Neurology, UHN, Division of Neurology, University of Toronto, Toronto, Ontario, Canada.

Motor Physiology and Neuromodulation Program, Division of Movement Disorders and Center for Health and Technology (CHeT), Department of Neurology, University of Rochester, Rochester, New York, USA.

出版信息

Mov Disord. 2021 Apr;36(4):999-1005. doi: 10.1002/mds.28407. Epub 2020 Nov 30.

Abstract

BACKGROUND

Celiac disease is associated with motor cortex hyperexcitability and neurological manifestations including cortical myoclonus. Electroencephalography abnormalities have been described, but no distinct pattern has been reported.

METHODS

We describe the neurophysiological characteristics of 3 patients with celiac-associated cortical myoclonus using electroencephalography, magnetoencephalography, and transcranial magnetic stimulation.

RESULTS

Electroencephalography in all cases demonstrated lateralized low-amplitude, electropositive beta-frequency polyspike activity over the central head region, corresponding to motor cortex contralateral to the myoclonic limb. Jerk-locked back-averaging demonstrated a preceding cortical potential; magnetoencephalography source localization revealed a cortical generator in the posterior wall of the precentral gyrus for the back-averaged potential and oscillatory abnormality. In 1 patient, cerebellar inhibition of the motor cortex was physiologically normal.

CONCLUSIONS

Central head oscillatory, low-amplitude, electropositive electroencephalography polyspike activity may be a distinct marker of celiac-related cortical myoclonus and is consistent with celiac-related motor cortex hyperexcitability, which may not necessarily result from cerebellar disinhibition. © 2020 International Parkinson and Movement Disorder Society.

摘要

背景

乳糜泻与运动皮层兴奋性过高有关,并伴有包括皮质肌阵挛在内的神经表现。脑电图异常已有描述,但尚未报道明确的模式。

方法

我们使用脑电图、脑磁图和经颅磁刺激描述了 3 例乳糜泻相关皮质肌阵挛患者的神经生理学特征。

结果

所有病例的脑电图均显示中央头部区域存在局灶性低振幅、正电性β频带多棘波活动,与肌阵挛肢体对侧的运动皮层相对应。肌阵挛锁定后平均显示皮质前电位;脑磁图源定位显示后扣带回皮质发生器与后平均电位和振荡异常相对应。在 1 例患者中,小脑对运动皮层的抑制是生理性正常的。

结论

中央头部振荡、低振幅、正电性脑电图多棘波活动可能是乳糜泻相关皮质肌阵挛的一个独特标志物,与乳糜泻相关的运动皮层兴奋性过高一致,而后者不一定是由于小脑去抑制引起的。© 2020 国际帕金森病和运动障碍学会。

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