中华神经医学杂志
中華神經醫學雜誌
중화신경의학잡지
CHINESE JOURNAL OF NEUROMEDICINE
2010年
2期
153-155
,共3页
刘仕勇%安宁%杨辉%侯智%杨梅华%魏宇佳%张伟
劉仕勇%安寧%楊輝%侯智%楊梅華%魏宇佳%張偉
류사용%안저%양휘%후지%양매화%위우가%장위
胚胎发育不良性神经上皮肿瘤%难治件癫痫%外科手术%皮质发育障碍
胚胎髮育不良性神經上皮腫瘤%難治件癲癇%外科手術%皮質髮育障礙
배태발육불량성신경상피종류%난치건전간%외과수술%피질발육장애
Dysembryoplastic neuroepithelial tumor%Intractable epilepsy%Surgery%Malformation in the cortical dysplasia
目的 探讨胚胎发育不良性神经上皮肿瘤(DNT)伴药物难治性癫痫患者的外科手术治疗方法.方法 回顾性分析了第三军医大学新桥医院神经外科采用外科手术治疗14例此类患者的经验.术前和术中均进行致痫灶定位,术中在切除肿瘤的同时一并处理肿瘤外致痫灶.结果 14例患者肿瘤均得到全切,未行放疗和化疗,无肿瘤复发及恶性转化.11例患者癫痫发作得到完全控制(Engel Ⅰ级),2例患者稀少发作(Engel Ⅱ级),1例患者术后仍有频繁癫痫发作,再次手术切除肿瘤周围致痫灶后癫痫得到完全控制.结论 DNT应当按照皮质发育障碍来处理,除切除肿瘤外,积极处理肿瘤外致痫灶可获得较佳的癫痫控制结果.
目的 探討胚胎髮育不良性神經上皮腫瘤(DNT)伴藥物難治性癲癇患者的外科手術治療方法.方法 迴顧性分析瞭第三軍醫大學新橋醫院神經外科採用外科手術治療14例此類患者的經驗.術前和術中均進行緻癇竈定位,術中在切除腫瘤的同時一併處理腫瘤外緻癇竈.結果 14例患者腫瘤均得到全切,未行放療和化療,無腫瘤複髮及噁性轉化.11例患者癲癇髮作得到完全控製(Engel Ⅰ級),2例患者稀少髮作(Engel Ⅱ級),1例患者術後仍有頻繁癲癇髮作,再次手術切除腫瘤週圍緻癇竈後癲癇得到完全控製.結論 DNT應噹按照皮質髮育障礙來處理,除切除腫瘤外,積極處理腫瘤外緻癇竈可穫得較佳的癲癇控製結果.
목적 탐토배태발육불량성신경상피종류(DNT)반약물난치성전간환자적외과수술치료방법.방법 회고성분석료제삼군의대학신교의원신경외과채용외과수술치료14례차류환자적경험.술전화술중균진행치간조정위,술중재절제종류적동시일병처리종류외치간조.결과 14례환자종류균득도전절,미행방료화화료,무종류복발급악성전화.11례환자전간발작득도완전공제(Engel Ⅰ급),2례환자희소발작(Engel Ⅱ급),1례환자술후잉유빈번전간발작,재차수술절제종류주위치간조후전간득도완전공제.결론 DNT응당안조피질발육장애래처리,제절제종류외,적겁처리종류외치간조가획득교가적전간공제결과.
Objective To investigate the management of drug-resistant epilepsy in patients with dysembryoplastic neuroepithelial tumor (DNT). Methods Surgical experiences of 14 patients with DNT in our hospital were retrospectively reviewed. According to the EeoG during the operation and preoperative evaluation, the epileptic foci were managed when the tumor resection was performed. Results The tumors were cut off completely in all the patients; no radiotherapy or chemotherapy was performed after the operation; no recurrence or metastasis of the tumor was found. Engel Ⅰ outcome (seizure-free) was noted in 11 patients and Engel Ⅱ outcome (rare seizure) was noted in 2; frequent seizure was found in 1 after the first operation and seizure-free was achieved after the resection of epileptic foci around the tumor. Conclusion The DNT should be treated as having malformation in the cortical dysplasia and management of epileptic foci around the tumor shows favorable results in the controlling of epilepsy.