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对患有结构性脑病变的韦斯特综合征及相关疾病中头皮快速(40 - 150赫兹)振荡的综合观察。

Complex observation of scalp fast (40-150 Hz) oscillations in West syndrome and related disorders with structural brain pathology.

作者信息

Kobayashi Katsuhiro, Endoh Fumika, Agari Takashi, Akiyama Tomoyuki, Akiyama Mari, Hayashi Yumiko, Shibata Takashi, Hanaoka Yoshiyuki, Oka Makio, Yoshinaga Harumi, Date Isao

机构信息

Department of Child Neurology Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences and Okayama University Hospital Okayama Japan.

Epilepsy Center Okayama University Hospital Okayama Japan.

出版信息

Epilepsia Open. 2017 Feb 21;2(2):260-266. doi: 10.1002/epi4.12043. eCollection 2017 Jun.

Abstract

We investigated the relationship between the scalp distribution of fast (40-150 Hz) oscillations (FOs) and epileptogenic lesions in West syndrome (WS) and related disorders. Subjects were 9 pediatric patients with surgically confirmed structural epileptogenic pathology (age at initial electroencephalogram [EEG] recording: mean 7.1 months, range 1-22 months). The diagnosis was WS in 7 patients, Ohtahara syndrome in 1, and a transitional state from Ohtahara syndrome to WS in the other. In the scalp EEG data of these patients, we conservatively detected FOs, and then examined the distribution of FOs. In five patients, the scalp distribution of FOs was consistent and concordant with the lateralization of cerebral pathology. In another patient, FOs were consistently dominant over the healthy cerebral hemisphere, and the EEG was relatively low in amplitude over the pathological atrophic hemisphere. In the remaining 3 patients, the dominance of FOs was inconsistent and, in 2 of these patients, the epileptogenic hemisphere was reduced in volume, which may result from atrophy or hypoplasia. The correspondence between the scalp distribution of FOs and the epileptogenic lesion should be studied, taking the type of lesion into account. The factors affecting scalp FOs remain to be elucidated.

摘要

我们研究了West综合征(WS)及相关疾病中快速(40 - 150Hz)振荡(FOs)的头皮分布与致痫性病变之间的关系。研究对象为9例经手术确诊有结构性致痫病理改变的儿科患者(首次脑电图[EEG]记录时的年龄:平均7.1个月,范围1 - 22个月)。其中7例诊断为WS,1例为大田原综合征,另1例为从大田原综合征向WS的过渡状态。在这些患者的头皮EEG数据中,我们保守地检测了FOs,然后检查了FOs的分布。5例患者中,FOs的头皮分布与脑病变的定位一致且相符。在另一例患者中,FOs始终在健康的大脑半球占主导,而在病理性萎缩半球上EEG的振幅相对较低。在另外3例患者中,FOs的优势并不一致,其中2例患者的致痫半球体积减小,这可能是萎缩或发育不全所致。应结合病变类型研究FOs的头皮分布与致痫性病变之间的对应关系。影响头皮FOs的因素仍有待阐明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e002/5719855/fb05d5d1a93f/EPI4-2-260-g001.jpg

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