Kirkpatrick P J, Honavar M, Janota I, Polkey C E
Neurosurgical Unit, Maudsley Hospital, London, England.
J Neurosurg. 1993 Jan;78(1):19-25. doi: 10.3171/jns.1993.78.1.0019.
Thirty-one patients with a mean age of 18.9 years (range 3 to 53 years) who underwent temporal lobe surgery for tumor-related epilepsy over a 14-year period are presented. All had suffered chronic drug-resistant temporal lobe seizures (mean age at onset 6.9 years, range 0 to 30 years; mean duration of condition 11.9 years, range 3 to 39 years). Preoperative interictal scalp electroencephalography tracings indicated unilateral localized epileptic foci in 90% of patients, and computerized tomography scans showed abnormalities within the temporal lobe in 87%. All patients underwent en bloc temporal lobectomy. No patient received adjuvant radiotherapy or chemotherapy. Review of the histological material showed dysembryoplastic neuroepithelial tumor in 27 (87%) of the specimens and microscopic evidence of incomplete removal of tumor in 22 (71%). At long-term follow-up evaluation (mean duration 5.8 years, range 1 to 14 years), 81% of patients were completely free of seizures (Engel grade I) and 10% were almost seizure free (Engel grade II) with no deaths reported in either early or late follow-up review. Only one patient in the series failed to benefit from the surgery. Four patients suffered permanent neurological deficit causing a mild disability. Psychological assessment showed no significant fall in verbal or performance intelligent quotient for the group, but a mild memory impairment was evident in 32%. Behavioral and social aspects improved in nearly all (94%) cases. Relief of seizures could not be predicted by intraoperative electrocorticography, and outcome was independent of the completeness of tumor resection. Postoperative electroencephalographic findings identified epileptiform potentials in 65% of patients, which were associated with a worse seizure-control outcome grade.
本文介绍了31例平均年龄18.9岁(范围3至53岁)的患者,他们在14年期间因肿瘤相关性癫痫接受了颞叶手术。所有患者均患有慢性耐药性颞叶癫痫(平均发病年龄6.9岁,范围0至30岁;平均病程11.9年,范围3至39年)。术前发作间期头皮脑电图描记显示90%的患者存在单侧局限性癫痫病灶,计算机断层扫描显示87%的患者颞叶内有异常。所有患者均接受了整块颞叶切除术。没有患者接受辅助放疗或化疗。对组织学材料的检查显示,27例(87%)标本为胚胎发育不良性神经上皮肿瘤,22例(71%)有肿瘤切除不完全的微观证据。在长期随访评估中(平均持续时间5.8年,范围1至14年),81%的患者完全无癫痫发作(恩格尔I级),10%的患者几乎无癫痫发作(恩格尔II级),早期或晚期随访均未报告死亡病例。该系列中只有1例患者未从手术中获益。4例患者出现永久性神经功能缺损,导致轻度残疾。心理评估显示该组患者的语言或操作智商没有显著下降,但32%的患者有轻度记忆障碍。几乎所有(94%)病例的行为和社会方面都有所改善。术中皮层脑电图无法预测癫痫发作的缓解情况,结果与肿瘤切除的完整性无关。术后脑电图检查发现65%的患者有癫痫样电位,这与较差的癫痫控制结果分级相关。