年轻女性癫痫性夜间漫游一例罕见病例报告及文献复习。

Q2 Medicine
Oman Medical Journal Pub Date : 2024-11-30 eCollection Date: 2024-11-01 DOI:10.5001/omj.2024.37
Alawi A Al-Attas, Attas A Al-Attas, Maryam A Al-Attas, Saleh K Swailem
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引用次数: 0

摘要

睡眠相关的多动性癫痫是夜间发生的额叶癫痫的常见症状。虽然颞叶引起的与睡眠有关的癫痫发作已被记录在案,但它们通常缺乏多动活动。此外,发作性夜间徘徊很少被观察到,被认为是一种不寻常的夜间癫痫形式,对抗癫痫药物有反应。在这个报告中,我们提出了一个14岁的右撇子女孩复发性梦游和徘徊的病例。间期脑电图显示左侧颞叶有致痫灶,该区域有间歇性慢波活动。在夜间游荡期间,患者表现出异常的暴力和非暴力行为,使自己处于轻微或严重伤害的危险之中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epileptic Nocturnal Wanderings in a Young Female: A Rare Case Report and Review of the Literature.

Sleep-related hyperkinetic seizures are a frequent symptom of frontal lobe epilepsy that occurs at night. Although temporal lobe-originating sleep-related seizures have been documented, they often lack hyperkinetic activity. Furthermore, episodic nocturnal wandering is rarely observed and is believed to represent an unusual form of nocturnal epilepsy that responds to anti-seizure medications. In this report, we present a case of a 14-year-old right-handed girl with recurrent sleepwalking and wandering. Interictal electroencephalography revealed an epileptogenic focus in the left temporal lobe and intermittent slow-wave activity originating from that region. During her nighttime wanderings, the patient exhibited unusually violent and nonviolent conduct, putting herself at risk of minor or serious injuries.

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来源期刊
Oman Medical Journal
Oman Medical Journal Medicine-Medicine (all)
CiteScore
3.10
自引率
0.00%
发文量
119
审稿时长
12 weeks
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