Maton Bruno, Resnick Trevor, Jayakar Prasanna, Morrison Glenn, Duchowny Michael
The Brain Institute, Miami Children's Hospital, 3200 S.W. 60th Court, Miami, FL 33155, USA.
Epilepsia. 2007 Aug;48(8):1485-90. doi: 10.1111/j.1528-1167.2007.01125.x. Epub 2007 Jun 12.
Gliomatosis cerebri (GC) is a rare neoplastic disorder that may present as intractable epilepsy during early life. We report our experience regarding the evaluation and the surgical treatment of epilepsy in this population.
All children evaluated between 1990 and 2006 for surgery of epilepsy (n = 741) with pathologically proven GC were selected.
We identified four male children with age at seizure onset ranging from 4 months to 11 years. Two had hemiparesis and one child with infantile spasms was developmentally delayed. Seizures occurred daily (n = 3) or monthly (n = 1). Ictal semiology was consistent with psychomotor seizures (n = 1), partial motor seizures (n = 2), and asymmetric epileptic spasms (n = 1). Surgery was symptomatic and aimed at debulking and controlling the epilepsy. Procedure was individually tailored based on the presurgical evaluation. Brain MRI revealed widespread hemispheric involvement (n = 3) or infiltration of the temporal lobe and basal ganglia (n = 1). Two patients were initially misdiagnosed as hemispheric cortical dysplasia and hemimegalencephaly. Scalp EEG was nonlocalizing in two cases, showed a right temporal focus in one case, and was not performed in one case. Interictal SPECT in one patient revealed widespread hemispheric hypoperfusion. Three cases were resected under ECoG guidance after a mean delay of 11 months after seizure onset. Following functional hemispherectomy (n = 1) or focal cortical resection (n = 2), all children were alive and seizure free with a mean follow-up of 48 months (2-5 years). No unexpected complication was reported. One nonoperated case was alive but still seizing after 15 months follow-up. Chemotherapy was associated in three cases.
GC is a rare cause of medically resistant epilepsy that may present in early life. The lack of a discrete lesion may lead to diagnostic uncertainty, especially in infancy. Epilepsy surgery is an effective therapy that can improve quality of life.
大脑胶质瘤病(GC)是一种罕见的肿瘤性疾病,在儿童早期可能表现为难治性癫痫。我们报告了我们在该人群中评估和手术治疗癫痫的经验。
选取1990年至2006年间接受癫痫手术评估(n = 741)且经病理证实为GC的所有儿童。
我们确定了4名男性儿童,癫痫发作起始年龄为4个月至11岁。2名有偏瘫,1名患婴儿痉挛症的儿童发育迟缓。癫痫发作频率为每日发作(n = 3)或每月发作(n = 1)。发作期症状学表现为精神运动性发作(n = 1)、部分运动性发作(n = 2)和不对称性癫痫痉挛(n = 1)。手术为对症治疗,旨在减少肿瘤体积并控制癫痫。手术程序根据术前评估进行个体化调整。脑部MRI显示广泛的半球受累(n = 3)或颞叶及基底节浸润(n = 1)。2例患者最初被误诊为半球性皮质发育异常和半侧巨脑症。头皮脑电图在2例中无定位意义,1例显示右侧颞叶病灶,1例未进行此项检查。1例患者发作间期单光子发射计算机断层扫描(SPECT)显示广泛的半球灌注减低。3例在癫痫发作起始后平均延迟11个月后在皮层脑电图(ECoG)引导下进行了切除。在接受功能性半球切除术(n = 1)或局灶性皮质切除术(n = 2)后,所有儿童均存活且无癫痫发作,平均随访48个月(2至5年)。未报告意外并发症。1例未手术的病例在随访15个月时仍存活但仍有癫痫发作。3例接受了化疗。
GC是儿童早期难治性癫痫的罕见病因。缺乏明确的病灶可能导致诊断不确定性,尤其是在婴儿期。癫痫手术是一种可改善生活质量的有效治疗方法。