Temporal encephalocele: An epileptogenic focus confirmed by direct intracranial electroencephalography

IF 1.8 Q3 CLINICAL NEUROLOGY Epilepsy and Behavior Reports Pub Date : 2023-01-01 DOI:10.1016/j.ebr.2023.100601
Shruti Agashe , Brian N. Lundstrom , Benjamin H. Brinkmann , Elson So , Gregory D. Cascino , Nicholas Gregg , W. Richard Marsh , Madeline Cross , Jamie J. Van Gompel , Kelsey M. Smith
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Abstract

Several studies have suggested the epileptogenic potential of temporal encephaloceles. However, there is limited literature describing the results of intracranial EEG monitoring for patients with temporal encephaloceles. We describe a 19 year-old right-handed woman with drug-resistant epilepsy who presented with seizure onset at age 16 in the setting of a left temporal encephalocele where the seizure onset zone was confirmed to be the encephalocele via stereo EEG (sEEG). She had focal impaired awareness seizures occurring weekly that would progress to focal to bilateral tonic-clonic seizures monthly. Imaging showed a left anterior inferior temporal lobe encephalocele and a left choroidal fissure cyst that were stable on repeat imaging. Prolonged scalp recorded video EEG recorded seizures that showed either near simultaneous onset in the bitemporal head regions or a transitional left temporal sharp wave followed by maximum evolution in the left temporal region. Invasive monitoring with sEEG electrodes targeting primarily the left limbic system with one electrode directly in the encephalocele captured seizures with onset in the left temporal pole encephalocele. A limited resection was performed based on the results of the sEEG and except for one seizure in the immediate postop period in the setting of infection, patient remains seizure free at her 4 month follow up. This report describes a case of drug-resistant focal epilepsy where sEEG monitoring confirmed a temporal encephalocele to be the seizure onset zone without simultaneous onset at mesial temporal or other neocortical structures that were sampled. Our findings support the potential for epileptogenicity within an encephalocele with direct intracranial monitoring.

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颞叶脑膨出:一种经直接颅内脑电图证实的致痫灶
几项研究表明颞叶脑膨出具有致痫潜力。然而,描述颞叶脑膨出患者颅内脑电图监测结果的文献有限。我们描述了一名患有耐药性癫痫的19岁右手女性,她在16岁时出现左侧颞叶脑膨出的癫痫发作,通过立体脑电图(sEEG)确认癫痫发作区为脑膨出。她每周都会发生局灶性意识障碍性癫痫发作,每月会发展为局灶性至双侧强直阵挛性癫痫发作。影像学检查显示左前颞下叶脑膨出和左脉络膜裂囊肿,重复影像学检查结果稳定。长时间头皮记录的视频脑电图记录的癫痫发作显示,双颞头部区域几乎同时发作,或者左颞尖波过渡,然后左颞区域出现最大演变。sEG电极的侵入性监测主要针对左边缘系统,其中一个电极直接位于脑膨出,捕捉到左颞极脑膨出发作的癫痫发作。根据sEG的结果进行了有限的切除,除了在感染的情况下在术后立即发作一次外,患者在4个月的随访中仍然没有发作。本报告描述了一例耐药局灶性癫痫,其中sEEG监测证实颞叶脑膨出是癫痫发作区,而取样的颞中或其他新皮质结构没有同时发作。我们的研究结果支持通过直接颅内监测在脑膨出内引起癫痫的可能性。
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来源期刊
Epilepsy and Behavior Reports
Epilepsy and Behavior Reports Medicine-Neurology (clinical)
CiteScore
2.70
自引率
13.30%
发文量
54
审稿时长
50 days
期刊最新文献
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