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亚慢波癫痫持续状态:在一名患有斯-韦综合征的儿童中记录到的一种新的亚临床癫痫持续状态形式。

Infraslow status epilepticus: A new form of subclinical status epilepticus recorded in a child with Sturge-Weber syndrome.

作者信息

Bello-Espinosa Luis E

机构信息

Department of Pediatrics, University of Calgary Faculty of Medicine, Calgary, Alberta, Canada; Department of Clinical Neurosciences, University of Calgary Faculty of Medicine, Calgary, Alberta, Canada; Alberta Children's Hospital Research Institute, University of Calgary Faculty of Medicine, Canada.

出版信息

Epilepsy Behav. 2015 Aug;49:193-7. doi: 10.1016/j.yebeh.2015.04.031. Epub 2015 Jun 20.

Abstract

BACKGROUND

Analysis of infraslow EEG activity (ISA) has shown potential in the evaluation of patients with epilepsy and in the differentiation between focal and generalized epilepsies. Infraslow EEG activity analysis may also provide insights into the pathophysiology of refractory clinical and subclinical status epilepticus. The purpose of this report is to describe a girl with Sturge-Weber syndrome (SWS) who presented with a 96-h refractory encephalopathy and nonischemic hemiparesis and who was identified to have infraslow status epilepticus (ISSE), which successfully resolved after midazolam administration.

METHODS

The continuous EEG recording of a 5-year-old girl with known structural epilepsy due to Sturge-Weber syndrome is presented. The patient presented to the ED with acute confusion, eye deviation, and right hemiparesis similar to two previous admissions. Despite administration of lorazepam, fosphenytoin, phenobarbital, and valproic loads, the patient showed no improvement in the clinical condition after 48 h. The continuous video-EEG monitoring (VEM) showed continuous severe diffuse nonrhythmic asymmetric slowing but no apparent ictal activity on continuous conventional EEG recording settings. As brain CT, CTA, CTV, and complete MRI scans including DWI obtained within 72 h of presentation failed to demonstrate any ischemic changes, analysis of the EEG infraslow (ISA) activity was undertaken using LFF: 0.01 Hz and HFF: of 0.1 Hz, respectively.

RESULTS

Continuous subclinical unilateral rhythmic ictal ISA was identified. This was only evident on the left hemisphere which correlated with the structural changes due to SWS. A trial of continuous 120 to 240 μg/kg/h of IV midazolam resulted in immediate resolution of the contralateral hemiparesis and encephalopathy.

CONCLUSION

Continuous prolonged rhythmic ictal infraslow activity (ISA) can cause super-refractory subclinical focal status epilepticus. This has not been previously reported, and we propose that this be called infraslow status epilepticus (ISSE). Infraslow EEG activity analysis should be performed in all patients with unexplained subclinical status epilepticus. This article is part of a Special Issue entitled "Status Epilepticus".

摘要

背景

超慢脑电活动(ISA)分析在癫痫患者评估以及局灶性和全身性癫痫的鉴别诊断中已显示出潜力。超慢脑电活动分析还可能为难治性临床和亚临床癫痫持续状态的病理生理学提供见解。本报告的目的是描述一名患有斯特奇-韦伯综合征(SWS)的女孩,她出现了96小时的难治性脑病和非缺血性偏瘫,并被确定患有超慢癫痫持续状态(ISSE),在给予咪达唑仑后成功缓解。

方法

呈现了一名因斯特奇-韦伯综合征导致已知结构性癫痫的5岁女孩的连续脑电图记录。该患者因急性意识模糊、眼球偏斜和右侧偏瘫就诊于急诊科,与之前的两次入院情况相似。尽管给予了劳拉西泮、磷苯妥英、苯巴比妥和丙戊酸负荷剂量,但患者在48小时后临床状况无改善。连续视频脑电图监测(VEM)显示持续严重的弥漫性非节律性不对称减慢,但在连续常规脑电图记录设置下未发现明显的发作期活动。由于在就诊后72小时内进行的脑部CT、CTA、CTV以及包括DWI在内的完整MRI扫描均未显示任何缺血性改变,因此分别使用低频滤波器(LFF):0.01Hz和高频滤波器(HFF):0.1Hz对脑电图超慢(ISA)活动进行分析。

结果

识别出连续的亚临床单侧节律性发作期ISA。这仅在左半球明显,与SWS引起的结构变化相关。连续静脉注射咪达唑仑120至240μg/kg/h的试验使对侧偏瘫和脑病立即得到缓解。

结论

连续长时间的节律性发作期超慢活动(ISA)可导致超难治性亚临床局灶性癫痫持续状态。此前未见报道,我们建议将其称为超慢癫痫持续状态(ISSE)。对于所有不明原因的亚临床癫痫持续状态患者均应进行超慢脑电活动分析。本文是名为“癫痫持续状态”的特刊的一部分。

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