儿童半球切除术患者自限性小儿局灶性癫痫(EDSelFEC)的癫痫样放电:白质异常的作用。

IF 1.9 4区 医学 Q3 CLINICAL NEUROLOGY Epileptic Disorders Pub Date : 2024-12-26 DOI:10.1002/epd2.20311
Oana Tarta-Arsene, Peter Winkler, Tom Pieper, Till Hartlieb, Andrea Zsoter, Irina Stan, Manfred Kudernatsch, Steffen Berweck, Hans Holthausen
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引用次数: 0

摘要

目的:探讨儿童脑半球切除术后与自限性局灶性癫痫(EDSelFEC)相关的癫痫样放电频率,评价同时存在EDSelFEC和结构性半球癫痫的患者与不同时存在EDSelFEC的患者是否存在差异,以及两组患者在术前处理和术后预后方面是否存在差异。方法:从癫痫中心的癫痫手术数据库中检索1999年1月至2015年1月期间接受半球切除术的131名儿童的数据。将EDSelFEC患儿与无EDSelFEC患儿在致痫性半球病理、家族史、癫痫发病年龄、手术时间、病变侧边性、术前认知功能、对钠通道阻滞剂抗癫痫药物的反应和手术结果等方面进行比较。获得了父母的同意。结果:131例脑电图中有27例(21%)存在edselec。没有患者出现与EDSelFECs相关的癫痫发作。不同病理组EDSelFECs的百分比不同:血管病变:38%,局灶性皮质发育不良:16%,多小脑回畸形:5%,拉斯穆森脑炎:10%,半大脑畸形:8%,轻度皮质发育畸形伴少突胶质细胞增生:20%,其他病理:22%。血管组的EDSelFEC与显示白质损伤和皮质损伤的MRI变化显著相关(p = 0.02)。82.1%的EDSelFEC多灶性,而非EDSelFEC的ed多灶性为4.8%。钠通道阻滞剂比结构(皮质)病变引起的EDs更容易加重EDSelFEC。EDSelFEC+和EDSelFEC-患者在研究的其他变量方面没有发现差异。意义:有相当数量的半球癫痫性病变的儿童,特别是有产前/围产期血管病变、偏瘫和白质病变的儿童,除了皮质病变外,还存在共存的EDSelFEC。
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Epileptiform discharges in the context of self-limited pediatric focal epilepsy (EDSelFEC) in pediatric hemispherotomy patients: Role of white matter abnormalities.

Objective: To investigate the frequency of epileptiform discharges associated with self-limited focal epilepsy (EDSelFEC) in children who have undergone a hemispherotomy and to evaluate whether patients with coexistence of EDSelFEC and structural hemispheric epilepsies differ from patients without coexistence of EDSelFEC and whether there are differences between the two groups with regard to preoperative management and postoperative outcome.

Methods: Data on 131 children who underwent a hemispherotomy between January 1999 and January 2015 were retrieved from the Epilepsy center's epilepsy surgery database. Children with EDSelFEC were compared with children without EDSelFEC with respect to epileptogenic hemispheric pathology, family history, age at epilepsy onset, timing of surgery, lesion laterality, preoperative cognitive function, response to sodium channel blocker antiepileptic medication, and surgical outcome. Parental consent was obtained.

Results: EDSelFECs were present in the EEG in 27 (21%) of the 131 cases. None of the patients had seizures associated with EDSelFECs. The percentages of EDSelFECs varied between pathology groups: vascular lesions: 38%, focal cortical dysplasia: 16%, polymicrogyria: 5%, Rasmussen encephalitis: 10%, hemimegalencephaly: 8%, mild malformation of cortical development with oligodendroglial hyperplasia:20%, other pathologies: 22%. EDSelFEC in the vascular group were significantly correlated with MRI changes showing white matter damage in addition to cortical damage (p =.02). 82.1% of EDSelFEC were located multifocal versus 4.8% multifocality in EDs other than EDSelFEC. EDSelFEC were significantly more often exacerbated by sodium channel blockers than EDs caused by structural (cortical) lesions. No differences were found between EDSelFEC+ and EDSelFEC- patients with respect to other variables studied.

Significance: A significant number of children with hemispheric epileptogenic lesions, particularly children with pre-/perinatal vascular lesions, hemiplegia, and white matter lesions in addition to cortical lesions, presented with coexisting EDSelFEC.

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来源期刊
Epileptic Disorders
Epileptic Disorders 医学-临床神经学
CiteScore
4.10
自引率
8.70%
发文量
138
审稿时长
6-12 weeks
期刊介绍: Epileptic Disorders is the leading forum where all experts and medical studentswho wish to improve their understanding of epilepsy and related disorders can share practical experiences surrounding diagnosis and care, natural history, and management of seizures. Epileptic Disorders is the official E-journal of the International League Against Epilepsy for educational communication. As the journal celebrates its 20th anniversary, it will now be available only as an online version. Its mission is to create educational links between epileptologists and other health professionals in clinical practice and scientists or physicians in research-based institutions. This change is accompanied by an increase in the number of issues per year, from 4 to 6, to ensure regular diffusion of recently published material (high quality Review and Seminar in Epileptology papers; Original Research articles or Case reports of educational value; MultiMedia Teaching Material), to serve the global medical community that cares for those affected by epilepsy.
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