Gomceli Y B, Erdem A, Bilir E, Kutlu G, Kurt S, Erden E, Karatas A, Erbas C, Serdaroglu A
Ministry of Health Ankara Training and Research Hospital, Department of Neurology, Ankara, Turkey.
Acta Neurol Belg. 2006 Mar;106(1):9-14.
High resolution MRI is very important in the evaluations of patients with intractable temporal lobe epilepsy in preoperative investigations. Morphologic abnormalities on cranial MRI usually indicate the epileptogenic focus. Intractable TLE patients who have normal cranial MRI or bilateral hippocampal atrophy may have a chance for surgery if a certain epileptogenic focus is determined. We evaluated the patients who were monitorized in Gazi University Medical Faculty Epilepsy Center from October 1997 to April 2004. Seventy three patients, who had a temporal epileptogenic focus, underwent anterior temporal lobectomy at Ankara University Medical Faculty Department of Neurosurgery. Twelve of them (16, 4%), did not have any localizing structural lesion on cranial MRI. Of the 12 patients examined 6 had normal findings and 6 had bilateral hippocampal atrophy. Of these 12 patients, 6 (50%) were women and 6 (50%) were men. The ages of patients ranged from 7 to 37 (mean: 24.5). Preoperatively long-term scalp video-EEG monitoring, cranial MRI, neuropsychological tests, and Wada test were applied in all patients. Five patients, whose investigations resulted in conflicting data, underwent invasive monitoring by the use of subdural strips. The seizure outcome of patients were classified according to Engel with postsurgical follow-up ranging from 11 to 52 (median: 35.7) months. Nine patients (75%) were classified into Engel's Class I and the other 3 patients (25%) were placed into Engel's Class II. One patient who was classified into Engel's Class II had additional psychiatric problems. The other patient had two different epileptogenic foci independent from each other in her ictal EEG. One of them localized in the right anterior temporal area, the other was in the right frontal lobe. She was classified in Engel's Class II and had no seizure originating from temporal epileptic focus, but few seizures originating from the frontal region continued after the surgery. In conclusion, surgery was successful in all 12 patients. We think that patients with no MRI lateralizing or localizing lesion should undergo epilepsy surgery after detailed presurgical evaluations, including invasive monitoring.
高分辨率磁共振成像在难治性颞叶癫痫患者的术前评估中非常重要。头颅磁共振成像上的形态学异常通常提示致痫灶。头颅磁共振成像正常或双侧海马萎缩的难治性颞叶癫痫患者,如果确定了特定的致痫灶,可能有手术机会。我们评估了1997年10月至2004年4月在加齐大学医学院癫痫中心接受监测的患者。73例有颞叶致痫灶的患者在安卡拉大学医学院神经外科接受了前颞叶切除术。其中12例(16.4%)头颅磁共振成像上没有任何定位结构性病变。在这12例接受检查的患者中,6例结果正常,6例有双侧海马萎缩。这12例患者中,6例(50%)为女性,6例(50%)为男性。患者年龄范围为7至37岁(平均:24.5岁)。所有患者术前均进行了长期头皮视频脑电图监测、头颅磁共振成像、神经心理学测试和Wada试验。5例检查结果相互矛盾的患者通过使用硬膜下条带进行了侵入性监测。根据Engel标准对患者的癫痫发作结果进行分类,术后随访时间为11至52个月(中位数:35.7个月)。9例(75%)患者被分类为Engel I级,其他3例(25%)患者被分类为Engel II级。1例被分类为Engel II级的患者有额外的精神问题。另1例患者在发作期脑电图中有两个相互独立的不同致痫灶。其中一个位于右侧前颞叶区域,另一个位于右侧额叶。她被分类为Engel II级,术后没有源自颞叶癫痫灶的发作,但仍有少数源自额叶区域的发作。总之,所有12例患者的手术均成功。我们认为,没有磁共振成像侧化或定位病变的患者在进行包括侵入性监测在内的详细术前评估后应接受癫痫手术。