中华神经外科杂志
中華神經外科雜誌
중화신경외과잡지
Chinese Journal of Neurosurgery
2010年
1期
40-43
,共4页
遇涛%张国君%李勇杰%蔡立新%王玉平%杜薇%朴媛媛
遇濤%張國君%李勇傑%蔡立新%王玉平%杜薇%樸媛媛
우도%장국군%리용걸%채립신%왕옥평%두미%박원원
癫痫%脑肿瘤%外科手术
癲癇%腦腫瘤%外科手術
전간%뇌종류%외과수술
Epilepsy%Brain neoplasms%Surgical procedures,operative
目的 分析伴顽固性癫痫患者的脑肿瘤病理特点,探讨最适合的手术方式.方法 在符合顽固性癫痫并进行手术治疗的病例中,回顾分析45例病理证实存在脑肿瘤的病例资料.结果 癫痫灶位于额叶8例,颞叶34例,顶枕叶3例;病理证实神经元和混合性神经元-胶质肿瘤35例(78%).WHO Ⅰ级36例,WHO Ⅰ~Ⅱ4例,WHO Ⅱ级5例.术后随访1年以上的42例,全部生存.癫痫发作控制结果 显示Engel Ⅰ级32例(76%),Ⅱ级5例,Ⅲ级4例,Ⅳ级1例.结论 与顽固性癫痫相关的脑肿瘤是一类特殊的病理组群,手术切除包括肿瘤在内的癫痫灶,效果满意.
目的 分析伴頑固性癲癇患者的腦腫瘤病理特點,探討最適閤的手術方式.方法 在符閤頑固性癲癇併進行手術治療的病例中,迴顧分析45例病理證實存在腦腫瘤的病例資料.結果 癲癇竈位于額葉8例,顳葉34例,頂枕葉3例;病理證實神經元和混閤性神經元-膠質腫瘤35例(78%).WHO Ⅰ級36例,WHO Ⅰ~Ⅱ4例,WHO Ⅱ級5例.術後隨訪1年以上的42例,全部生存.癲癇髮作控製結果 顯示Engel Ⅰ級32例(76%),Ⅱ級5例,Ⅲ級4例,Ⅳ級1例.結論 與頑固性癲癇相關的腦腫瘤是一類特殊的病理組群,手術切除包括腫瘤在內的癲癇竈,效果滿意.
목적 분석반완고성전간환자적뇌종류병리특점,탐토최괄합적수술방식.방법 재부합완고성전간병진행수술치료적병례중,회고분석45례병리증실존재뇌종류적병례자료.결과 전간조위우액협8례,섭협34례,정침협3례;병리증실신경원화혼합성신경원-효질종류35례(78%).WHO Ⅰ급36례,WHO Ⅰ~Ⅱ4례,WHO Ⅱ급5례.술후수방1년이상적42례,전부생존.전간발작공제결과 현시Engel Ⅰ급32례(76%),Ⅱ급5례,Ⅲ급4례,Ⅳ급1례.결론 여완고성전간상관적뇌종류시일류특수적병리조군,수술절제포괄종류재내적전간조,효과만의.
Objective To analyze the spectrum of neoplasms associated with refractory epilepsy and to evaluate the optimum surgical treatment of these patients. Method The clinical, electrophysiological, operative,and histopathological data of 45 patients who underwent surgery for medically intractable epilepsy were retrospectively evaluated. Results The majority of tumors were located in the temporal lobe(n = 34) and frontal lobe (n = 8). The most frequent tumors were neuronal and mixed neuronal-glial tumors (76%), including gangliocytoma or ganglioglioma(n = 15), dysembryoplastic neuroepithelial tumour(n = 7). All the tumors were low histopathological grade (WHO Ⅰ or Ⅱ). In all patients, complete resection of tumor and epileptogenic area was intended. Complications were encountered in 5 patients. Of the 45 patients who had postoperative follow-up more than one year, 78% were seizure-free and no patient died. Conclusions The neoplasms associated with medically intractable epilepsy constitute a distinct clinicopathological group of tumors. Complete surgical removal of the tumors and the epileptogenic area can achieve excellent seizure control