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探讨切除性癫痫手术对睡眠中癫痫性电持续状态儿童的效用:长期临床和电生理结果

Examining the Utility of Resective Epilepsy Surgery in Children With Electrical Status Epilepticus in Sleep: Long Term Clinical and Electrophysiological Outcomes.

作者信息

Marashly Ahmad, Koop Jennifer, Loman Michelle, Lee Yu-Wen, Lew Sean M

机构信息

Division of Pediatric Neurology, Children's Hospital of Wisconsin, Medical College of Wisconsin, Milwaukee, WI, United States.

Division of Pediatric Neuropsychology, Children's Hospital of Wisconsin, Medical College of Wisconsin, Milwaukee, WI, United States.

出版信息

Front Neurol. 2020 Jan 15;10:1397. doi: 10.3389/fneur.2019.01397. eCollection 2019.

DOI:10.3389/fneur.2019.01397
PMID:32010050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6974623/
Abstract

Electrical Status Epilepticus in Sleep (ESES) is an epileptic encephalopathy syndrome characterized by infrequent clinical seizures and prominent interictal burden during slow wave sleep associated with cognitive deficits and behavioral dysfunction. Medical treatment with anti-epileptic drugs is often unsuccessful. Resective surgery may be a valuable option in carefully selected patients. This case series aims to describe the indications, long term results and utility of resective surgery for ESES. Information on 14 patients who underwent surgery for epilepsy and ESES at the Children's Hospital of Wisconsin between 2007 and 2017 is included. Clinical, electrographic and neuropsychological features and outcomes are described in detail. The most common pathology was encephalomalacia due to perinatal middle cerebral artery stoke (5/14). Twelve patients had imaging findings of perinatal pathologies; however, two patients had normal magnetic resonance imaging. Surgery was performed to control refractory epilepsy in eight patients. Six patients had no clinical seizures for 1-6 years prior to surgery, one of which had no known clinical seizures at all. All showed cognitive declines (6/14) or impairment (8/14) on neuropsychological assessments, and surgery was suggested to minimize further cognitive declines. The most common surgical procedure was hemispherotomy (10/14). Temporo-parieto-occipital disconnection, frontal lobectomy, parieto-occipital resection, and limited corticectomy were also used, with good outcomes for the first three procedures. Clinical follow up mean was 4.4 years and 12 patients had excellent seizure outcome. Electroencephalography (EEG) follow up mean was 3 years and ESES resolved in 12/14 patients. All patients completed post-surgical neuropsychological evaluation with mean follow-up of 17.46 months. Resective surgery is an effective treatment for selected cases of ESES, producing long term seizure freedom, resolution of ESES and stabilization of cognitive and behavioral functioning in most patients. Our case series is the largest single center cohort description addressing resective surgery for ESES. Outcomes in this sample suggest that good long-term seizure, EEG and cognitive/behavioral outcomes can be achieved in patients with normal brain imaging and in limited lobar or multi-lobar resections. Moreover, patients with ESES and very infrequent clinical seizures can benefit from surgery with stabilization of cognitive and behavioral functioning.

摘要

睡眠期癫痫性电持续状态(ESES)是一种癫痫性脑病综合征,其特征为临床发作不频繁,且在慢波睡眠期有明显的发作间期负荷,伴有认知缺陷和行为功能障碍。使用抗癫痫药物进行药物治疗往往不成功。对于精心挑选的患者,切除性手术可能是一种有价值的选择。本病例系列旨在描述ESES切除性手术的适应症、长期结果及效用。纳入了2007年至2017年间在威斯康星儿童医院接受癫痫和ESES手术的14例患者的信息。详细描述了其临床、脑电图及神经心理学特征和结果。最常见的病理改变是围生期大脑中动脉卒中导致的脑软化(5/14)。12例患者有围生期病变的影像学表现;然而,2例患者磁共振成像正常。8例患者进行手术以控制难治性癫痫。6例患者在手术前1至6年无临床发作,其中1例根本没有已知的临床发作。所有患者在神经心理学评估中均显示认知下降(6/14)或受损(8/14),建议手术以尽量减少进一步的认知下降。最常见的手术方式是大脑半球切除术(10/14)。还采用了颞顶枕叶离断术、额叶切除术、顶枕叶切除术和局限性皮质切除术,前三种手术方式效果良好。临床随访平均时间为4.4年,12例患者癫痫发作结果良好。脑电图(EEG)随访平均时间为3年,14例患者中有12例ESES得到缓解。所有患者均完成了术后神经心理学评估,平均随访时间为17.46个月。切除性手术是治疗部分ESES病例的有效方法,能使大多数患者长期无癫痫发作、ESES得到缓解且认知和行为功能稳定。我们的病例系列是针对ESES切除性手术的最大单中心队列描述。该样本中的结果表明,脑成像正常的患者以及进行有限叶或多叶切除的患者可实现良好的长期癫痫发作、脑电图及认知/行为结果。此外,ESES且临床发作非常不频繁的患者可从手术中获益,认知和行为功能得以稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/777e/6974623/1ec5b62ecc12/fneur-10-01397-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/777e/6974623/68f48a35ff8b/fneur-10-01397-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/777e/6974623/a0eb923676fd/fneur-10-01397-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/777e/6974623/1ec5b62ecc12/fneur-10-01397-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/777e/6974623/68f48a35ff8b/fneur-10-01397-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/777e/6974623/a0eb923676fd/fneur-10-01397-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/777e/6974623/1ec5b62ecc12/fneur-10-01397-g0003.jpg

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