Takahashi Akio, Hong Seung-Chyul, Seo Dae Won, Hong Seung Bong, Lee Munhyang, Suh Yeon-Lim
Department of Neurosurgery, Gunma University School of Medicine, Maebashi, Japan.
Surg Neurol. 2005 Nov;64(5):419-27. doi: 10.1016/j.surneu.2005.02.005.
We report on our experience with epilepsy surgery in the treatment of localization-related epilepsy caused by dysembryoplastic neuroepithelial tumor (DNT) aimed at achieving the best seizure control.
A retrospective analysis was performed on the pathological reports as well as on clinical data of 24 case patients with medically intractable epilepsy with DNT treated surgically between 1995 and 2000 at the Samsung Medical Center. Resective surgery was performed using subdural electrodes or intraoperative electrocorticography in all patients.
The mean follow-up period was 57.2 months. Two patients had rare seizures transiently after surgery but remained free from seizures after 6 months. Others remained completely free from seizures. There was a strong tendency of temporal lobe involvement (19 cases; 79.2%). Size of tumors located at medial temporal regions was significantly smaller than those at lateral temporal or frontal lobes (P < .05). A rather radical resection (tumor plus surrounding tissue showing active epileptogenicity) was performed in all but one case where only focal lesionectomy was done. In 20 of the 24 cases (83.3%), association of cortical dysplasia (CD) was found on pathological examination.
We conclude that DNT is frequently associated with CD, with a wide area of epileptogenic activity that might be related to the presence of CD around the DNT. Comprehensive preoperative investigations for accurate localization of epileptogenic activity, meticulous brain mapping, and a rather radical resection of pathological areas might be essential for the achievement of excellent seizure control in DNT-associated epilepsy.
我们报告了我们在癫痫手术治疗由胚胎发育不良性神经上皮肿瘤(DNT)引起的局灶性相关性癫痫方面的经验,旨在实现最佳的癫痫控制。
对1995年至2000年在三星医疗中心接受手术治疗的24例药物难治性癫痫伴DNT患者的病理报告和临床数据进行回顾性分析。所有患者均使用硬膜下电极或术中皮质脑电图进行切除手术。
平均随访期为57.2个月。2例患者术后短暂出现罕见癫痫发作,但6个月后无癫痫发作。其他患者一直无癫痫发作。有强烈的颞叶受累倾向(19例;79.2%)。位于颞叶内侧区域的肿瘤大小明显小于颞叶外侧或额叶的肿瘤(P <.05)。除1例仅行局灶性病灶切除术外,所有病例均进行了较为彻底的切除(肿瘤加周围显示有活性致痫性的组织)。24例中有20例(83.3%)在病理检查中发现合并皮质发育异常(CD)。
我们得出结论,DNT常与CD相关,具有广泛的致痫活性区域,这可能与DNT周围CD的存在有关。全面的术前检查以准确定位致痫活性、细致的脑图谱绘制以及对病理区域进行较为彻底的切除对于实现DNT相关性癫痫的良好癫痫控制可能至关重要。