Ohara K, Morita Y, Takauchi S, Takeda T, Hayashi S
Department of neuropsychiatry, Hyogo college of medicine, Japan.
Rinsho Shinkeigaku. 1996 Aug;36(8):962-7.
Attacks of gelastic (laughing) seizure are usually reported as complex partial seizures of temporal lobe epilepsy and seizures associated with hypothalamic hamartomas, but are rarely reported as complex partial seizures of frontal lobe origin. We recently encountered a 29-year-old woman who had gelastic seizure attacks from age 17. She had shown severe mental retardation with cerebral palsy at 7 months, and entered precocious puberty at age 7. Attacks of gelastic seizure with ipsilateral adversive seizures, ipsilateral oculogyric crisis, and horizontal epileptic nystagmus were observed until her death at age 29. Each gelastic seizure lasted 1 to 10 minutes. Her laughing was very strong and loud. Interictal spikes were observed over the right fronto-parietal lobe, but no ictal spike was detected. The neuropathological examinations of her brain revealed no hypothalamic lesions such as hamartomas, gliosis, and distinct neuronal loss. Her brain was severely affected with multicystic encephalopathy, and the bilateral temporal lobe tissues were almost replaced by the cystic changes. The right frontal lobe and occipital lobe were not cystic. From the clinicopathological examinations, the focus of her gelastic seizure was considered to be of the right frontal origin. The hippocampus and parahippocampal gyrus are major components of the limbic system, which is involved in affective emotions. Although the right hippocampus and parahippocampal gyrus were completely lost, and those of the left hemisphere were almost completely lost, by the multicystic replacements in this case, the gelastic seizure attacks were evoked from right frontal origin. The frontal lobe may play an important role in motor expressions of laughing. The motor expressions of the loud and strong laughing may be one of the characteristic features of frontal lobe-originated gelastic seizure of this case.
笑性癫痫发作通常被报道为颞叶癫痫的复杂部分性发作以及与下丘脑错构瘤相关的发作,但很少被报道为额叶起源的复杂部分性发作。我们最近遇到一名29岁女性,她从17岁起就有笑性癫痫发作。她在7个月大时就出现了严重智力发育迟缓并伴有脑瘫,7岁时进入性早熟。在她29岁去世前,观察到她有伴有同侧扭转性发作、同侧动眼危象和水平性癫痫性眼球震颤的笑性癫痫发作。每次笑性癫痫发作持续1至10分钟。她的笑声非常强烈且响亮。在右侧额顶叶观察到发作间期棘波,但未检测到发作期棘波。对她的大脑进行神经病理学检查未发现下丘脑病变,如错构瘤、胶质增生和明显的神经元丢失。她的大脑严重受多囊性脑病影响,双侧颞叶组织几乎被囊性改变所取代。右侧额叶和枕叶没有囊性变。从临床病理检查来看,她笑性癫痫的病灶被认为起源于右侧额叶。海马体和海马旁回是边缘系统的主要组成部分,边缘系统与情感情绪有关。尽管在这个病例中,右侧海马体和海马旁回因多囊性替代而完全消失,左侧半球的也几乎完全消失,但笑性癫痫发作仍由右侧额叶起源引发。额叶可能在笑的运动表达中起重要作用。大声且强烈的笑的运动表达可能是该病例额叶起源笑性癫痫的特征之一。