Boon P, Calliauw L, De Reuck J, Hoksbergen I, Achten E, Thiery E, Caemaert J, De Somer A, Decoo D
Department of Neurology, University Hospital, Gent, Belgium.
Acta Neurochir (Wien). 1994;128(1-4):68-83. doi: 10.1007/BF01400655.
Twenty patients (13 males, 7 females), who presented with refractory partial epilepsy and a CT and/or MR detected intracranial intra-axial structural lesion were admitted to the University of Gent Epilepsy Monitoring Unit. Mean duration of the epilepsy was 17 years (2-47 years). All patients were enrolled in a comprehensive presurgical protocol including neurological examination, video-scalp-EEG monitoring with prolonged interictal and ictal recording, neuropsychological assessment and positron emission tomography (PET). Intracranial EEG monitoring was performed in 5 patients in whom discrepancies between different tests were found during the non-invasive evaluation. Clinical neurological examination was normal in 16 patients; 4 patients had a mild contralateral hemiparesis. Lesions were mainly located in the temporal lobe (55%). Most patients presented with complex partial seizures (90%). Clinical seizure characteristics correlated well with the lesion location in 55% of patients. Interictal EEG showed focal epileptic activity and focal slowing in respectively 85% and 30% of patients. Interictal EEG lateralization was congruent with the side of the lesion in 17 patients (85%). Interictal EEG localization was congruent with the lobe of the lesion in 13 patients (65%). Ictal EEG lateralized correctly in 14 patients (70%) and localized correctly in 10 patients (50%). Neuropsychological assessment lateralized and localized congruently in respectively 8/17 (47%) and 7/17 (41%) of patients. Interictal PET showed focal interictal hypometabolism, congruent with the lesion, in 13/16 (81%) of patients. Intracranial EEG was congruent with the lesion location in 3 patients but non-congruent in 2 patients. All patients underwent surgical procedures: average follow-up was 14 months (6-24 months). Complete surgical removal of the lesion with free margins resulted in a more than 90% reduction of seizures without postoperative neurological deficit in 12/13 patients.
20例患者(13例男性,7例女性)因难治性部分性癫痫且CT和/或磁共振成像(MR)检测到颅内轴内结构性病变,被收治于根特大学癫痫监测病房。癫痫平均病程为17年(2 - 47年)。所有患者均纳入了全面的术前方案,包括神经学检查、长时间发作间期和发作期记录的视频头皮脑电图(EEG)监测、神经心理学评估以及正电子发射断层扫描(PET)。5例在无创评估期间发现不同检查结果存在差异的患者进行了颅内EEG监测。16例患者临床神经学检查正常;4例患者有轻度对侧偏瘫。病变主要位于颞叶(55%)。大多数患者表现为复杂部分性发作(90%)。55%的患者临床发作特征与病变位置相关性良好。发作间期EEG分别在85%和30%的患者中显示局灶性癫痫样活动和局灶性慢波。发作间期EEG的定侧与17例患者(85%)病变侧一致。发作间期EEG的定位与13例患者(65%)病变所在脑叶一致。发作期EEG在14例患者(70%)中正确定侧,在10例患者(50%)中正确定位。神经心理学评估在分别8/17(47%)和7/17(41%)的患者中定侧和定位一致。发作间期PET在13/16(81%)的患者中显示与病变一致的局灶性发作间期代谢减低。颅内EEG与3例患者的病变位置一致,但与2例患者不一致。所有患者均接受了手术治疗:平均随访时间为14个月(6 - 24个月)。12/13例患者通过完整切除病变且切缘阴性,癫痫发作减少超过90%,且术后无神经功能缺损。