Chibane Imane Samah, Boucher Olivier, Dubeau François, Tran Thi Phuoc Yen, Mohamed Ismail, McLachlan Richard, Sadler R Mark, Desbiens Richard, Carmant Lionel, Nguyen Dang Khoa
Division of Neurology, CHUM Notre-Dame, Université de Montréal, Québec, Canada.
Department of Psychology, Université de Montréal, Québec, Canada.
Epilepsy Behav. 2017 Nov;76:32-38. doi: 10.1016/j.yebeh.2017.08.038. Epub 2017 Sep 18.
Orbitofrontal epilepsy (OFE) is less known and is poorly characterized in comparison with temporal lobe epilepsy, partly because it is rare and possibly because it is unrecognized and therefore underestimated.
This paper aimed to better characterize seizure semiology, presurgical findings, and surgical outcomes in patients with OFE.
We retrospectively reviewed all confidently established OFE cases from six Canadian epilepsy monitoring units between 1988 and 2014, and in the literature between 1972 and 2017. Inclusion criteria were identification of an epileptogenic lesion localized in the OFC or if the patient was seizure-free after surgical removal of the OFC in nonlesional cases.
Sixteen cases were identified from our databases. Fifty percent had predominantly sleep-related seizures; 56% had no aura (the remaining had nonspecific or vegetative auras), and 62.5% featured hypermotor (mostly hyperkinetic) behaviors. Interictal epileptiform discharges over frontal and temporal derivations always allowed lateralization. Magnetic resonance imaging (MRI) identified an orbitofrontal lesion in 8/16, positron emission tomography (PET) identified a hypometabolism extending outside the orbital cortex in 4/9, ictal single-photon emission computed tomography (SPECT) identified an orbital hyperperfusion in 1/5, magnetoencephalography (MEG) identified lateral orbital sources in 2/4, and intracranial electroencephalography (EEG) identified an orbitofrontal onset in 9/10. Fourteen patients underwent surgery, all reaching a favorable outcome (71.4% Engel 1; 28.6% Engel 2; mean FU=5.6years). Pre- and postoperative neuropsychological assessments revealed heterogeneous findings. Our review of literature identified 71 possible cases of OFE, 32 with confident focus localization. Extracted data from these cumulated cases supported observations made from our case series.
Orbitofrontal epilepsy should be suspected with sleep-related, hyperkinetic seizures with no specific aura, and frontotemporal interictal discharges. Several patients have nonmotor seizures with or without auras which may resemble temporal lobe seizures. Postoperative seizure outcome was favorable, but there is inherent bias as we only included patients with a seizure-free outcome if the MRI was negative. A larger study is required to address identified gaps in knowledge such as identifying discriminative features between medial and lateral OFE, evaluating the value of more recent diagnostic tools, and assessing the neuropsychological outcome of orbital epilepsy surgery.
眶额癫痫(OFE)相比颞叶癫痫鲜为人知且特征描述不足,部分原因是其罕见,也可能是未被识别因而被低估。
本文旨在更好地描述OFE患者的发作症状学、术前检查结果及手术效果。
我们回顾性分析了1988年至2014年间来自加拿大6个癫痫监测单位以及1972年至2017年间文献中所有确诊的OFE病例。纳入标准为确定致痫性病变位于眶额皮质(OFC),或在非病变性病例中患者在手术切除OFC后无癫痫发作。
从我们的数据库中识别出16例病例。50%的患者主要发作与睡眠相关;56%无先兆(其余有非特异性或植物神经先兆),62.5%有运动增多(大多为多动)行为。额部和颞部导联的发作间期癫痫样放电总能实现定侧。磁共振成像(MRI)在16例中的8例发现眶额病变,正电子发射断层扫描(PET)在9例中的4例发现代谢减低延伸至眶皮质外,发作期单光子发射计算机断层扫描(SPECT)在5例中的1例发现眶部血流灌注增加,脑磁图(MEG)在4例中的2例发现眶外侧来源,颅内脑电图(EEG)在10例中的9例发现眶额起始部位。14例患者接受了手术,均取得良好效果(恩格尔1级占71.4%;恩格尔2级占28.6%;平均随访时间=5.6年)。术前和术后神经心理学评估结果各异。我们对文献的回顾确定了71例可能为OFE的病例,其中32例病灶定位明确。从这些累积病例中提取的数据支持了我们病例系列中的观察结果。
对于与睡眠相关、多动且无特定先兆以及额颞部发作间期放电的癫痫发作,应怀疑为眶额癫痫。部分患者有或无先兆的非运动性发作,可能类似于颞叶癫痫发作。术后癫痫发作结果良好,但存在固有偏差,因为我们仅纳入了MRI阴性且无癫痫发作的患者。需要开展更大规模的研究以填补已发现的知识空白;如确定内侧和外侧OFE之间的鉴别特征、评估更新的诊断工具的价值以及评估眶额癫痫手术的神经心理学结果。