Lombardi D, Marsh R, de Tribolet N
Department of Neurosurgery, University Hospital of Geneva, Switzerland.
Acta Neurochir Suppl. 1997;68:70-4. doi: 10.1007/978-3-7091-6513-3_13.
In approximately 30% of patients with intractable partial epilepsy, an intra-axial cerebral lesion is the aetiology of the seizure disorder. Lesions adjacent to mesiotemporal structures often result in secondary epileptogenicity in the same region. The authors present 22 cases of low-grade gliomas associated with intractable epilepsy. In 15 cases the location was temporal (8 extra-hippocampal and 7 with invasion of the amygdalo-hippocampus), 7 cases were extratemporal in eloquent areas. The eight extra-hippocampal tumours were originally treated with lesionectomy. The seizure outcome was class 1 in only 4 cases, the remaining 4 were class 4 according to Engel's classification. The 4 cases with class 4 outcome required additional temporal lobectomy associated with amygdalo-hippocampectomy for seizure control. The 2 cases with associated hippocampal atrophy at MRI after lobectomy had outcome class 1. The 2 cases without hippocampal atrophy at MRI presented outcome class 2. The 7 cases with invasion of amygdala and hippocampus were treated with selective lesionectomy+amygdalo-hippocampectomy. In all these cases convergence of focal structural abnormality, ictal onset of epileptiform EEG abnormality and interictal epileptiform EEG abnormality provided powerful evidence of focal epileptogenicity. All these patients had a favourable epilepsy outcome (class 1-2). In the seven extratemporal cases the first step was lesionectomy. In 1 case located in the parietal region intraoperative mapping was required. 5 had class 1 outcome, one case had outcome class 2 and one case had an outcome class 4. The last patient required a second step operation with intraoperative strip and deep electrode monitoring that led subsequently to a frontal lobectomy. This patient is seizure free 2 years after surgery. There was no perioperative mortality and post-operative morbidity was 3/22. This study indicates that lesionectomy may be the first step procedure if the structural abnormality is localized to extra-temporal eloquent cortex and concordance is documented. Patients may subsequently be candidates for a cortical resection as a second step procedure if the lesionectomy does not provide an adequate reduction in seizure tendency. Since MRI identified hippocampal atrophy was predictive in this study of an unsatisfactory seizure outcome after lesionectomy, MRI defined dual pathologies consisting of a temporal lesion plus hippocampal atrophy necessitate temporal lobectomy+amygdalo-hippocampectomy. In patients with negative MRI findings of hippocampal atrophy and temporal lobe lesions, intraoperative electrocorticography and deep electrode monitoring are indicated for planning the surgical strategy.
在约30%的难治性部分性癫痫患者中,轴内脑病变是癫痫发作障碍的病因。靠近颞叶内侧结构的病变常导致同一区域的继发性致痫性。作者报告了22例与难治性癫痫相关的低级别胶质瘤病例。其中15例位于颞叶(8例位于海马体外,7例侵犯杏仁核 - 海马),7例位于非颞叶的功能区。8例海马体外肿瘤最初接受了病灶切除术。根据恩格尔分类,仅4例发作结果为1级,其余4例为4级。4例结果为4级的患者需要额外进行颞叶切除术并联合杏仁核 - 海马切除术以控制癫痫发作。叶切除术后MRI显示有海马萎缩的2例患者发作结果为1级。MRI无海马萎缩的2例患者发作结果为2级。7例侵犯杏仁核和海马的患者接受了选择性病灶切除术 + 杏仁核 - 海马切除术。在所有这些病例中,局灶性结构异常、癫痫样脑电图异常的发作期起始和发作间期癫痫样脑电图异常的汇聚为局灶性致痫性提供了有力证据。所有这些患者的癫痫发作结果良好(1 - 2级)。在7例非颞叶病例中,第一步是病灶切除术。1例位于顶叶区域的病例术中需要进行图谱绘制。5例发作结果为1级,1例为2级,1例为4级。最后1例患者需要第二步手术,术中使用条状电极和深部电极监测,随后进行了额叶切除术。该患者术后2年无癫痫发作。围手术期无死亡病例,术后发病率为3/22。本研究表明,如果结构异常局限于非颞叶功能区皮质且有记录显示一致性,则病灶切除术可能是第一步手术。如果病灶切除术不能充分降低癫痫发作倾向,患者随后可能作为第二步手术进行皮质切除术。由于在本研究中MRI发现的海马萎缩预示着病灶切除术后癫痫发作结果不理想,MRI确定的由颞叶病变加上海马萎缩组成的双重病变需要进行颞叶切除术 + 杏仁核 - 海马切除术。对于MRI海马萎缩和颞叶病变结果为阴性的患者,术中皮层脑电图和深部电极监测可用于制定手术策略。