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Laugh-induced seizure: a case report

机译:笑引起的癫痫发作:一例报告

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Introduction 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. Case presentation 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. Conclusions 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.
机译:引言笑引起的癫痫发作是一种无法识别的疾病,据我们所知,到目前为止,医学文献中尚未报道过任何病例。我们提出了一个有趣且极为罕见的案例,在该案例中,笑声引起了癫痫发作,该癫痫发作被视频脑电图记录并确认。病例介绍一名43岁的肥胖白种人男子,患有双相情感障碍和慢性头痛,伴有多发癫痫发作,这些发作都是在观看喜剧节目时的笑声引起的。每个情节持续约五秒钟。在每种情况下,他都开始大笑,然后双臂开始颤抖,他感到“他的意识被吸走了”。体格检查显示正常结果。他因双相情感障碍而接受丙戊酸治疗,而因慢性头痛而接受托吡酯治疗,但这并不能控制他的症状。他的睡眠剥夺性脑电图和脑磁共振成像正常,只是右前中颅窝的蛛网膜囊肿尺寸为4.2×2.1cm。他的视频脑电图显示了笑引起的癫痫发作活动。然后将他放在卡马西平上。治疗后,他有两次轻度凝视但没有坦率的癫痫发作,并且在这种治疗方案下他的癫痫发作一直得到良好控制。结论大笑诱发的癫痫发作是最不寻常的临床表现,没有任何以前的病例报告。可以通过视频脑电图记录笑声引起的癫痫发作活动来进行确诊。就像在没有下丘脑错构瘤的全突性癫痫发作中一样,我们的病例对使用托吡酯和卡马西平的多药疗法反应良好,避免了嘲笑。需要进一步研究以建立这种情况的标准治疗方法。

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