Department of Pediatrics, Wayne State University School of Medicine, Children's Hospital of Michigan, Detroit Medical Center, Detroit, Michigan, U.S.A; Department of Neurology, Wayne State University School of Medicine, Children's Hospital of Michigan, Detroit Medical Center, Detroit, Michigan, U.S.A.
Epilepsia. 2014 Dec;55(12):1926-33. doi: 10.1111/epi.12845. Epub 2014 Nov 3.
Cortical resections in epilepsy surgery tend to be larger in children, compared to adults, partly due to underlying pathology. Some children show unilateral multifocal seizure onsets involving much of the hemisphere. If there were a significant hemiparesis present, hemispherectomy would be the procedure of choice. Otherwise, it is preferable to spare the primary sensorimotor cortex. We report the results of "subtotal" hemispherectomy in 23 children.
All children (ages 1 year and 4 months to 14 years and 2 months) were operated on between 2001 and 2013 at Children's Hospital of Michigan (Detroit). Patients were evaluated with scalp video-electroencephalography (EEG), magnetic resonance imaging (MRI), (18) F-fluorodeoxyglucose-positron emission tomography (FDG-PET) scans, and neuropsychological assessments when applicable. Subsequently, each case was discussed in a multidisciplinary epilepsy surgery conference, and a consensus was reached pertaining to candidacy for surgery and optimum surgical approach. The actual extent of resection was based on the results from subdural electrocorticography (ECoG) monitoring. The surgical outcome is based on International League Against Epilepsy (ILAE) classification (class 1-6).
Among the 23 patients, 11 had epileptic spasms as their major seizure type; these were associated with focal seizures in 3 children. MRI showed focal abnormalities in 12 children. FDG-PET was abnormal in all but one subject. All except two children underwent chronic subdural ECoG. Multiple subpial transections were performed over the sensorimotor cortex in three subjects. On histopathology, various malformations were seen in 9 subjects; the remainder showed gliosis alone (n = 12), porencephaly (n = 1), and gliosis with microglial activation (n = 1). Follow-up ranged from 13 to 157 months (mean = 65 months). Outcomes consisted of class 1 (n = 17, 74%), class 2 (n = 2), class 3 (n = 1), class 4 (n = 1), and class 5 (n = 2).
Extensive unilateral resections sparing only sensorimotor cortex can be performed with excellent results in seizure control. Even with the presence of widespread unilateral epileptogenicity or anatomic/functional imaging abnormalities, complete hemispherectomy can often be avoided, particularly when there is little hemiparesis.
与成年人相比,癫痫手术中的皮质切除术在儿童中往往更大,部分原因是潜在的病理。一些儿童表现为单侧多灶性癫痫发作,涉及大脑半球的大部分。如果存在明显的偏瘫,那么半球切除术将是首选的手术方法。否则,最好保留初级感觉运动皮层。我们报告了 23 名儿童“次全”半球切除术的结果。
所有儿童(年龄 1 岁 4 个月至 14 岁 2 个月)均于 2001 年至 2013 年在密歇根儿童医院(底特律)接受手术。对患者进行头皮视频脑电图(EEG)、磁共振成像(MRI)、(18)氟-脱氧葡萄糖正电子发射断层扫描(FDG-PET)扫描和神经心理学评估(如适用)。随后,在多学科癫痫手术会议上讨论了每个病例,并就手术适应证和最佳手术方法达成共识。实际切除范围基于硬膜下皮质电图(ECoG)监测结果。手术结果基于国际抗癫痫联盟(ILAE)分类(1-6 级)。
在 23 名患者中,11 名以癫痫痉挛为主要发作类型;其中 3 名患儿伴有局灶性发作。12 名患儿 MRI 显示局灶性异常。除 1 名患者外,所有患者均进行 FDG-PET 检查异常。除 2 名患儿外,所有患儿均行慢性硬膜下 ECoG。3 名患儿的感觉运动皮质上进行了多次软膜下横切。组织病理学检查显示 9 名患儿存在各种畸形;其余患儿仅表现为胶质增生(n=12)、脑穿通畸形(n=1)和胶质增生伴小胶质细胞激活(n=1)。随访时间为 13 至 157 个月(平均 65 个月)。结果包括 1 级(n=17,74%)、2 级(n=2)、3 级(n=1)、4 级(n=1)和 5 级(n=2)。
在控制癫痫发作方面,可以进行广泛的单侧切除,仅保留感觉运动皮层,效果极佳。即使存在广泛的单侧致痫性或解剖/功能成像异常,也通常可以避免完全半球切除术,尤其是当偏瘫程度较轻时。