Spontaneous Intracranial Hypotension Presenting with Chiari Malformation and Hydrocephalus Associated With Lumbar Pseudoarachnoiditis

Carter Lacey M, Gross Naina L
{"title":"Spontaneous Intracranial Hypotension Presenting with Chiari Malformation and Hydrocephalus Associated With Lumbar Pseudoarachnoiditis","authors":"Carter Lacey M, Gross Naina L","doi":"10.36959/595/420","DOIUrl":null,"url":null,"abstract":"Spontaneous intracranial hypotension (SIH) is a rare occurrence, especially in children. In the pediatric population, three cases of Chiari malformation in children and no cases of hydrocephalus due to SIH have been discussed in the literature. We present two patients under the age of five who presented with imaging concerning for the need for neurosurgical intervention later found to be due to SIH that resolved spontaneously.","PeriodicalId":432995,"journal":{"name":"Journal of Pediatric Neurology and Neuroscience","volume":"25 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Neurology and Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36959/595/420","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Spontaneous intracranial hypotension (SIH) is a rare occurrence, especially in children. In the pediatric population, three cases of Chiari malformation in children and no cases of hydrocephalus due to SIH have been discussed in the literature. We present two patients under the age of five who presented with imaging concerning for the need for neurosurgical intervention later found to be due to SIH that resolved spontaneously.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
自发性颅内低血压表现为腰椎假性蛛网膜炎相关的奇亚里畸形和脑积水
自发性颅内低血压(SIH)是罕见的发生,特别是在儿童。在儿童人群中,文献中讨论了三例儿童基亚里氏畸形,而没有一例由于SIH引起的脑积水。我们报告了两名五岁以下的患者,他们在影像学上表现出需要神经外科干预,后来发现是由于SIH自发消退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Wernicke Encephalopathy in a Non-Alcoholic Obese Adolescent: A Case Report Treatment of Bi-Allelic PRRT-2 Mutation Associated Ataxia and Paroxysmal Dyskinesia Unusual Diagnosis and Extended Management of Chronic Inflammatory Demyelinating Polyneuropathy in an Unimmunized Patient Treatment of COVID Encephalitis in Pediatric Patient with IVIG Reversible Cerebral Vasoconstriction Syndrome following Exchange Transfusion and Steroids in a Child with Sickle Cell Disease: A Case Report
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1