Mainali Naba Raj, Jalota Leena, Aryal Madan Raj, Schmidt Torrey R, Badal Madan, Alweis Richard
Department of Medicine, Reading Health System, Sixth Avenue and Spruce Street, West Reading, PA, 19611, USA.
J Med Case Rep. 2013 May 13;7:123. doi: 10.1186/1752-1947-7-123.
A laugh-induced seizure is an unrecognized condition and to the best of our knowledge no case has been reported in the medical literature until now. We present an interesting and extremely rare case in which laughing generated the seizure activity that was recorded and confirmed by video electroencephalography.
A 43-year-old obese Caucasian man with history of bipolar disorder and chronic headache presented with multiple episodes of seizures, all induced by laughter while watching comedy shows. Each episode lasted approximately five seconds. In each instance, he started laughing, then his arms started shaking and he felt like 'his consciousness was being vacuumed away'. A physical examination revealed normal findings. He had been maintained on valproic acid for bipolar disorder and topiramate for his chronic headache, but this did not control his symptoms. His sleep-deprived electroencephalography and brain magnetic resonance imaging were normal except for an arachnoid cyst measuring 4.2 × 2.1cm in the anterior right middle cranial fossa. His video electroencephalography demonstrated laugh-induced seizure activities. He was then placed on carbamazepine. Following treatment, he had two episodes of mild staring but no frank seizures, and his seizures have remained well controlled on this regimen for more than a year.
Laugh-induced seizure is a most unusual clinical entity without any previous case report. Confirmatory diagnosis can be made by video electroencephalography recording of seizure activities provoked by laughing. As in gelastic seizure without hypothalamic hamartoma, our case responded well to polytherapy with topiramate and carbamazepine on top of laugh-provocation avoidance. Further study is required to establish the standard treatment of this condition.
笑诱发性癫痫是一种未被认识的病症,据我们所知,迄今为止医学文献中尚无相关病例报道。我们在此呈现一例有趣且极为罕见的病例,其中大笑引发了癫痫活动,该活动通过视频脑电图记录并得到证实。
一名43岁的肥胖白人男性,有双相情感障碍和慢性头痛病史,出现多次癫痫发作,均在观看喜剧节目时因大笑诱发。每次发作持续约五秒。在每个发作实例中,他开始大笑,然后手臂开始颤抖,并且感觉“自己的意识被抽空”。体格检查结果正常。他一直服用丙戊酸治疗双相情感障碍,服用托吡酯治疗慢性头痛,但这并未控制住他的症状。除了右侧中颅窝前部有一个4.2×2.1厘米的蛛网膜囊肿外,他的睡眠剥夺脑电图和脑磁共振成像均正常。他的视频脑电图显示有笑诱发性癫痫活动。随后他开始服用卡马西平。治疗后,他有两次轻度凝视发作,但无明显癫痫发作,并且在该治疗方案下癫痫已得到良好控制超过一年。
笑诱发性癫痫是一种极为罕见的临床病症,此前无病例报道。通过记录大笑诱发的癫痫活动的视频脑电图可做出确诊。如同无下丘脑错构瘤的痴笑性癫痫一样,我们的病例在避免大笑诱发的基础上,联合使用托吡酯和卡马西平进行多药治疗效果良好。需要进一步研究以确立该病症的标准治疗方法。