Koutroumanidis Michalis, Tsirka Vasiliki, Panayiotopoulos Chrysostomos
Clinical Neurophysiology Dpt., Epilepsy, Guys, St Thomas' NHS Foundation Trust, Department of Academic Neurosciences, Kings College London, London, UK.
Clinical Neurophysiology Dpt., Epilepsy, Guys, St Thomas' NHS Foundation Trust.
Epileptic Disord. 2015 Sep;17(3):275-86. doi: 10.1684/epd.2015.0765.
To evaluate the clinical associations of adult-onset photosensitivity, we studied the clinical and EEG data of patients who were referred due to a possible first seizure and who had a photoparoxysmal response on their EEG. Patients with clinical evidence of photosensitivity before the age of 20 were excluded. Of a total of 30 patients, four had acute symptomatic seizures, two had vasovagal syncope, and 24 were diagnosed with epilepsy. Nine of the 24 patients had idiopathic (genetic) generalized epilepsies and predominantly generalized photoparoxysmal response, but also rare photically-induced seizures, while 15 had exclusively, or almost exclusively, reflex photically-induced occipital seizures with frequent secondary generalization and posterior photoparoxysmal response. Other important differences included a significantly older age at seizure onset and paucity of spontaneous interictal epileptic discharges in patients with photically-induced occipital seizures; only a quarter of these had occasional occipital spikes, in contrast to the idiopathic (genetic) generalized epilepsy patients with typically generalized epileptic discharges. On the other hand, both groups shared a positive family history of epilepsy, common seizure threshold modulators (such as tiredness and sleep deprivation), normal neurological examination and MRI, a generally benign course, and good response to valproic acid. We demonstrated that photosensitivity can first occur in adult life and manifest, either as idiopathic (possibly genetic) photosensitive occipital epilepsy with secondary generalization or as an EEG, and less often, a clinical/EEG feature of idiopathic (genetic) generalized epilepsies. Identification of idiopathic photosensitive occipital epilepsy fills a diagnostic gap in adult first-seizure epileptology and is clinically important because of its good response to antiepileptic drug treatment and fair prognosis.
为评估成人期光敏性的临床关联,我们研究了因首次癫痫发作可能而转诊且脑电图有光阵发性反应的患者的临床和脑电图数据。排除20岁之前有光敏性临床证据的患者。在总共30例患者中,4例有急性症状性癫痫发作,2例有血管迷走性晕厥,24例被诊断为癫痫。24例患者中有9例患有特发性(遗传性)全身性癫痫,主要为全身性光阵发性反应,但也有罕见的光诱发性癫痫发作,而15例患者仅有或几乎仅有反射性光诱发性枕叶癫痫发作,伴有频繁的继发性泛化和枕后光阵发性反应。其他重要差异包括光诱发性枕叶癫痫发作患者的癫痫发作起始年龄显著较大且发作间期自发性癫痫放电较少;这些患者中只有四分之一偶尔有枕叶棘波,这与典型全身性癫痫放电的特发性(遗传性)全身性癫痫患者形成对比。另一方面,两组患者都有癫痫家族史阳性、常见的癫痫发作阈值调节因素(如疲劳和睡眠剥夺)、神经系统检查和磁共振成像正常、病程一般良性以及对丙戊酸反应良好。我们证明光敏性可首次出现在成年期,并表现为特发性(可能为遗传性)光敏性枕叶癫痫伴继发性泛化,或作为脑电图表现,较少情况下作为特发性(遗传性)全身性癫痫的临床/脑电图特征。特发性光敏性枕叶癫痫的识别填补了成人首次发作癫痫学中的诊断空白,因其对抗癫痫药物治疗反应良好且预后较好,在临床上具有重要意义。