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首页> 外文期刊>Epilepsia: Journal of the International League against Epilepsy >A case with atypical childhood occipital epilepsy 'Gastaut type': an ictal migraine manifestation with a good response to intravenous diazepam.
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A case with atypical childhood occipital epilepsy 'Gastaut type': an ictal migraine manifestation with a good response to intravenous diazepam.

机译:儿童非典型枕型癫痫病“ Gastaut型”:一例偏头痛表现,对静脉注射地西epa反应良好。

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We report the history of a 14-year-old girl with atypical childhood occipital epilepsy "Gastaut type" whose first generalized tonic-clonic seizure was preceded by migraine without aura and followed by a status migrainosus. This status lasted for 3 days despite standard analgesic therapy. An EEG recording revealed an occipital status epilepticus during her migraine complaints. Seven minutes after intravenous administration of 10 mg diazepam under continuous EEG recording, a suppression of the epileptiform discharges over the right occipital was seen, while the headache subsided 3 min later. After precise questioning about the circumstances that possibly could have led to these events, it appeared that she had played for hours with a play station on the new color TV and she had visited an exhibition of Matisse and Bonnard with bright colors and contrast-rich text. Standardized extensive intermittent photic stimulation (IPS), 2 days after the status migrainosus, evoked besides asymmetrical right-sided driving, green spots in her left visual field, while in the EEG sharp waves were recorded over the right parietotemporal region. After further IPS with 20 Hz (eye closure), she started complaining of a light pulsating headache right occipitally and in the EEG right parietotemporal sharp-waves were seen. This lasted for about 10 min. Later, an interictal routine EEG was normal except for some theta over the right temporooccipital area. The most likely diagnosis is an atypical form of occipital epilepsy "Gastaut type." We would therefore advocate recording EEGs with photic stimulation in patients with atypical migraneous features.
机译:我们报道了一个14岁女孩的历史,该女孩患有非典型的儿童枕型癫痫病“ Gastaut型”,其首次广泛性强直阵挛性癫痫发作之前是先兆无先兆性偏头痛,然后是偏头痛状态。尽管进行了常规的止痛治疗,这种状态仍持续了3天。脑电图记录显示,在偏头痛发作期间,枕骨状态持续发作。在连续的脑电图记录下静脉注射10mg地西epa后7分钟,右枕骨的癫痫样放电被抑制,而头痛在3分钟后消退。在对可能导致这些事件的情况进行了精确的询问之后,似乎她已经在新彩色电视上的游戏台上玩了几个小时,并且参观了马蒂斯和波纳德的展览,这些展览的色彩鲜艳且对比鲜明。 。偏头痛状态发生两天后,除了不对称的右侧驾驶外,还诱发了标准的广泛间歇性光刺激(IPS),左侧视野中出现绿点,而在脑电图中,右颞叶颞区记录到剧烈的波浪。在以20 Hz的频率进一步进行IPS(闭眼)后,她开始抱怨轻度的脉动性头痛,并在脑电图中发现了右顶颞颞尖波。这持续了大约10分钟。后来,除右侧颞枕区域的一些θ外,发作间期常规脑电图正常。最可能的诊断是枕型癫痫病的一种典型形式。因此,我们建议在具有非典型迁移特征的患者中记录具有光刺激的脑电图。

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