在没有典型MRI表现的情况下,Rasmussen综合征的功能性半球切除术

Yasunori Nagahama , Charuta Joshi , Brian Dlouhy , Angela Y. Wu , Taylor J. Abel , Gary Baumbach , Hiroto Kawasaki
{"title":"在没有典型MRI表现的情况下,Rasmussen综合征的功能性半球切除术","authors":"Yasunori Nagahama ,&nbsp;Charuta Joshi ,&nbsp;Brian Dlouhy ,&nbsp;Angela Y. Wu ,&nbsp;Taylor J. Abel ,&nbsp;Gary Baumbach ,&nbsp;Hiroto Kawasaki","doi":"10.1016/j.ebcr.2016.11.003","DOIUrl":null,"url":null,"abstract":"<div><p>A 7-year-old previously healthy girl presented with a left-sided focal seizure without impaired consciousness and subsequently developed epilepsia partialis continua. Initial MRI was normal, and the subsequent images only showed a focal T2/FLAIR hyperintense area without cortical atrophy. She was diagnosed with Rasmussen syndrome by pathology and promptly treated with functional hemispherotomy. Rasmussen syndrome is a rare progressive neurological disorder, the only definitive cure for which is hemispheric disconnection. The disease presents a management dilemma, especially early in disease course without characteristic neuroimaging features. A high index of suspicion, multidisciplinary approach, and clear timely communication with the family are critical.</p></div>","PeriodicalId":56365,"journal":{"name":"Epilepsy and Behavior Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.ebcr.2016.11.003","citationCount":"5","resultStr":"{\"title\":\"Functional hemispherotomy in Rasmussen syndrome in the absence of classic MRI findings\",\"authors\":\"Yasunori Nagahama ,&nbsp;Charuta Joshi ,&nbsp;Brian Dlouhy ,&nbsp;Angela Y. Wu ,&nbsp;Taylor J. Abel ,&nbsp;Gary Baumbach ,&nbsp;Hiroto Kawasaki\",\"doi\":\"10.1016/j.ebcr.2016.11.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A 7-year-old previously healthy girl presented with a left-sided focal seizure without impaired consciousness and subsequently developed epilepsia partialis continua. Initial MRI was normal, and the subsequent images only showed a focal T2/FLAIR hyperintense area without cortical atrophy. She was diagnosed with Rasmussen syndrome by pathology and promptly treated with functional hemispherotomy. Rasmussen syndrome is a rare progressive neurological disorder, the only definitive cure for which is hemispheric disconnection. The disease presents a management dilemma, especially early in disease course without characteristic neuroimaging features. A high index of suspicion, multidisciplinary approach, and clear timely communication with the family are critical.</p></div>\",\"PeriodicalId\":56365,\"journal\":{\"name\":\"Epilepsy and Behavior Case Reports\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.ebcr.2016.11.003\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Epilepsy and Behavior Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2213323216300809\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Epilepsy and Behavior Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213323216300809","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

摘要

一个7岁的健康女孩表现为左侧局灶性癫痫,没有意识受损,随后发展为部分连续性癫痫。最初的MRI正常,随后的图像仅显示局灶性T2/FLAIR高信号区,无皮质萎缩。病理诊断为拉斯穆森综合征,并及时行功能性半球切开术治疗。拉斯穆森综合征是一种罕见的进行性神经系统疾病,唯一有效的治疗方法是大脑半球断开。该疾病呈现出一个管理困境,特别是在病程早期没有特征性的神经影像学特征。高度的怀疑、多学科的方法和与家人及时明确的沟通是至关重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Functional hemispherotomy in Rasmussen syndrome in the absence of classic MRI findings

Functional hemispherotomy in Rasmussen syndrome in the absence of classic MRI findings

Functional hemispherotomy in Rasmussen syndrome in the absence of classic MRI findings

Functional hemispherotomy in Rasmussen syndrome in the absence of classic MRI findings

A 7-year-old previously healthy girl presented with a left-sided focal seizure without impaired consciousness and subsequently developed epilepsia partialis continua. Initial MRI was normal, and the subsequent images only showed a focal T2/FLAIR hyperintense area without cortical atrophy. She was diagnosed with Rasmussen syndrome by pathology and promptly treated with functional hemispherotomy. Rasmussen syndrome is a rare progressive neurological disorder, the only definitive cure for which is hemispheric disconnection. The disease presents a management dilemma, especially early in disease course without characteristic neuroimaging features. A high index of suspicion, multidisciplinary approach, and clear timely communication with the family are critical.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信