Epilepsy Center, Cleveland Clinic, Cleveland, Ohio; Division of Pediatric Epilepsy, Minnesota Epilepsy Group, P.A., St. Paul, Minnesota; Department of Pediatric Neurology, Children's Hospitals and Clinics of Minnesota, St. Paul, Minnesota.
Epilepsy Center, Cleveland Clinic, Cleveland, Ohio.
Pediatr Neurol. 2018 Jan;78:13-19. doi: 10.1016/j.pediatrneurol.2017.09.009. Epub 2017 Sep 19.
Magnetoencephalography has emerged as a tool for preoperative evaluation in children. We studied magnetoencephalography characteristics in subtypes of focal cortical dysplasia and correlated the findings with postoperative seizure outcome.
Inclusion criteria were children ≤18 years who underwent magnetoencephalography during the preoperative evaluation followed by epilepsy surgery and a histopathologic diagnosis of focal cortical dysplasia between February 2008 and February 2013. Patient demographics, MRI, video electroencephalography, and magnetoencephalography data were reviewed. Postoperative seizure outcome data were categorized per International League against Epilepsy definitions.
Of 178 magnetoencephalography studies performed in children during the study period, 33 patients met inclusion criteria. Focal cortical dysplasia type I, II, and III were found on histopathology in 52%, 39%, and 9% of patients, respectively. Thirty patients had positive magnetoencephalography dipoles, including all patients with focal cortical dysplasia type II and III and 82% of patients with focal cortical dysplasia type I. Three patients had magnetoencephalography unique spikes. Brain MRI lesions were noted preoperatively in 21 patients (64%). Twenty-three patients (77%) had surgical resection of magnetoencephalography dipoles and 11 (48%) of them achieved favorable outcome.
Magnetoencephalography supplemented scalp electroencephalography data in spike source localization and showed unique spikes in 10% of the focal cortical dysplasia patients. Magnetoencephalography spikes and tight magnetoencephalography clusters were found more frequently in patients with focal cortical dysplasia type II and III as compared with focal cortical dysplasia type I. Presence of an MRI lesion and complete versus incomplete resection of magnetoencephalography cluster did not result in significant difference in postoperative seizure outcome, likely reflecting selection bias of doing magnetoencephalography in only difficult-to-localize epilepsies.
脑磁图已成为儿童术前评估的一种工具。我们研究了局灶性皮质发育不良各亚型的脑磁图特征,并将这些发现与术后癫痫发作结果相关联。
纳入标准为 2008 年 2 月至 2013 年 2 月期间在接受癫痫手术且组织病理学诊断为局灶性皮质发育不良的≤18 岁儿童中,行术前评估期间进行脑磁图检查的患者。回顾患者的人口统计学、MRI、视频脑电图和脑磁图数据。术后癫痫发作结果按照国际抗癫痫联盟的定义进行分类。
在研究期间,对 178 例行脑磁图检查的儿童中,有 33 例患者符合纳入标准。组织病理学发现局灶性皮质发育不良 I 型、II 型和 III 型分别占 52%、39%和 9%。30 例患者存在阳性脑磁图偶极子,包括所有局灶性皮质发育不良 II 型和 III 型患者和 82%的局灶性皮质发育不良 I 型患者。3 例患者存在脑磁图独特棘波。21 例患者(64%)术前存在脑 MRI 病变。23 例(77%)患者行脑磁图偶极子切除术,其中 11 例(48%)患者术后结果良好。
脑磁图补充了头皮脑电图数据在棘波源定位中的作用,并在 10%的局灶性皮质发育不良患者中发现了独特棘波。与局灶性皮质发育不良 I 型相比,局灶性皮质发育不良 II 型和 III 型患者更常出现脑磁图棘波和紧密的脑磁图簇。存在 MRI 病变和脑磁图簇的完全或不完全切除与术后癫痫发作结果无显著差异,这可能反映了仅在难以定位的癫痫中进行脑磁图检查的选择偏倚。