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儿童多阶段癫痫手术中致痫性新皮质病变切除术后的有创监测

Invasive monitoring after resection of epileptogenic neocortical lesions in multistaged epilepsy surgery in children.

作者信息

Hidalgo Eveline Teresa, Frankel Hyman Gregory, Rodriguez Crystalann, Orillac Cordelia, Phillips Sophie, Patel Neel, Devinsky Orrin, Friedman Daniel, Weiner Howard L

机构信息

Division of Pediatric Neurosurgery, Department of Neurosurgery, NYU Langone Health, New York, USA.

Division of Pediatric Neurosurgery, Department of Neurosurgery, NYU Langone Health, New York, USA.

出版信息

Epilepsy Res. 2018 Dec;148:48-54. doi: 10.1016/j.eplepsyres.2018.09.001. Epub 2018 Sep 19.

Abstract

OBJECTIVE

Incomplete resection of neocortical epileptogenic foci correlates with failed epilepsy surgery in children. We often treat patients with neocortical epilepsy with a staged approach using invasive monitoring to localize the focus, resect the seizure onset zone, and, in select cases, post-resection invasive monitoring (PRM). We report the technique and the outcomes of children treated with staged surgery including PRM.

METHODS

We retrospectively reviewed the charts of pediatric patients with neocortical epilepsy who underwent resective surgery with PRM.

RESULTS

We identified 71 patients, 5 patients with MRI-negative epilepsy and 66 patients with MRI-identified neocortical lesions; 64/66 (97%) patients had complete lesionectomy. In 61/71 (86%) patients PRM was associated with positive outcomes. Those findings were: 1) clinical seizures with electrographic involvement at resection margins (47%); 2) subclinical seizures and interictal discharges at resection margins (29%); and 3) clinical and subclinical seizures revealing a new epileptogenic focus (20%). In 55/71 (77%) patients, PRM data led to additional resection (re-resection; RR). Six additional patients had no further resection due to overlap with eloquent cortex. Histopathology showed tuberous sclerosis complex (TSC; n = 46), focal cortical dysplasia (FCD; n = 16)), gliosis (n = 4), tumors (n = 4), and Sturge-Weber syndrome (n = 1). There were no major complications. Seizure-free outcome in children with TSC was 63% at 1-year follow-up and 56% at 2-year follow-up. In FCD, seizure freedom after 1 and 2 years was 85%.

SIGNIFICANCE

Post-resection monitoring may provide additional information about the extent of the epileptogenic zone, such as residual epileptogenic activity at the margins of the resection cavity, and may unmask additional seizure foci. This method may be especially useful in achieving long-term stable seizure-free outcome.

摘要

目的

新皮质癫痫病灶切除不完全与儿童癫痫手术失败相关。我们经常采用分阶段方法治疗新皮质癫痫患者,通过侵入性监测来定位病灶、切除癫痫发作起始区,并在某些情况下进行切除后侵入性监测(PRM)。我们报告采用包括PRM在内的分阶段手术治疗儿童的技术及结果。

方法

我们回顾性分析了接受PRM切除手术的新皮质癫痫儿科患者的病历。

结果

我们确定了71例患者,5例MRI阴性癫痫患者和66例MRI发现新皮质病变的患者;66例患者中有64例(97%)进行了完全病灶切除术。71例患者中有61例(86%)PRM取得了阳性结果。这些结果包括:1)切除边缘有临床发作且伴有脑电图异常(47%);2)切除边缘有亚临床发作和发作间期放电(29%);3)临床和亚临床发作揭示新的癫痫病灶(20%)。71例患者中有55例(77%),PRM数据导致了额外切除(再次切除;RR)。另外6例患者因与明确的皮质重叠而未进一步切除。组织病理学显示结节性硬化症(TSC;n = 46)、局灶性皮质发育不良(FCD;n = 16)、胶质增生(n = 4)、肿瘤(n = 4)和斯-韦综合征(n = 1)。无重大并发症。TSC患儿1年随访时无癫痫发作的结局为63%,2年随访时为56%。FCD患儿1年和2年后无癫痫发作的比例为85%。

意义

切除后监测可能提供有关癫痫病灶范围的额外信息,例如切除腔边缘的残留癫痫活动,并可能发现额外的癫痫病灶。该方法对于实现长期稳定的无癫痫发作结局可能特别有用。

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