Luan Lan, Sun Yuqiang, Yang Kang
Department of Neurosurgery, The Second Hospital of Dalian Medical University, Dalian, Liaoning 116000, P.R. China.
Department of Neurosurgery, The Central Hospital of Harbin, Harbin, Heilongjiang 150000, P.R. China.
Exp Ther Med. 2018 Dec;16(6):4886-4892. doi: 10.3892/etm.2018.6774. Epub 2018 Sep 19.
Coexistence of hippocampal sclerosis (HS) and a temporal neocortical lesion, including focal cortical dysplasia, vascular malformations or benign primary brain tumors, is defined as dual pathology. In the majority of cases, the complete evidence based on electroencephalogram (EEG) and magnetic resonance imaging (MRI) for each of the dual pathological lesions is difficult to obtain. As a result, patients with dual pathology are poor surgical candidates due to potential incomplete resection of the epileptogenic zone. The current study retrospectively reviewed 24 patients with potential dual pathology and incomplete EEG and MRI evidence, aiming to provide novel surgical strategies. The results revealed a significantly worse seizure-free outcome for patients with incomplete EEG and MRI data compared with patients who received a clear diagnosis of dual pathology based on complete test results (11.1 vs. 60.0%; P<0.05). Notably, satisfying surgical (seizure-free) outcomes were still achieved in 60% of patients with unclear EEGs to locate the onset zone and clear MRI scans identifying the sclerotic hippocampus and nearby neocortical lesions, which could be resected together. In patients with multiple epileptogenic onsets or with widespread epileptic discharges, the hippocampus should be spared from resection due to concern for potential postsurgical mood or memory disorders. In conclusion, patients with resection of the sclerotic hippocampus and neocortical lesion had improved seizure-free outcomes compared with patients who received individual lesion resection. The current study aimed to provide a novel surgical strategy for neurosurgeons treating epileptic patients with dual pathology.
海马硬化(HS)与颞叶新皮质病变(包括局灶性皮质发育异常、血管畸形或原发性脑良性肿瘤)并存被定义为双重病理。在大多数情况下,很难获得基于脑电图(EEG)和磁共振成像(MRI)的关于每种双重病理病变的完整证据。因此,由于癫痫发作起始区可能无法完全切除,双重病理的患者不是手术的理想候选者。本研究回顾性分析了24例具有潜在双重病理且EEG和MRI证据不完整的患者,旨在提供新的手术策略。结果显示,与基于完整检查结果明确诊断为双重病理的患者相比,EEG和MRI数据不完整的患者无癫痫发作的预后明显更差(11.1%对60.0%;P<0.05)。值得注意的是,在60%的EEG不清楚无法定位发作起始区但MRI扫描清晰显示硬化海马体和附近新皮质病变且可一并切除的患者中,仍取得了令人满意的手术(无癫痫发作)效果。对于有多个癫痫发作起始点或有广泛癫痫放电的患者,由于担心术后可能出现情绪或记忆障碍,应避免切除海马体。总之,与单独切除病变的患者相比,切除硬化海马体和新皮质病变的患者无癫痫发作的预后有所改善。本研究旨在为神经外科医生治疗双重病理的癫痫患者提供一种新的手术策略。