Acute Brainstem Dysfunction Caused by Cavernous Sinus Dural Arteriovenous Fistula.

IF 0.9 Q4 CLINICAL NEUROLOGY
Case Reports in Neurological Medicine Pub Date : 2020-05-23 eCollection Date: 2020-01-01 DOI:10.1155/2020/2630959
Yuwa Oka, Kenichi Komatsu, Soichiro Abe, Naoya Yoshimoto, Junya Taki, Sadayuki Matsumoto
{"title":"Acute Brainstem Dysfunction Caused by Cavernous Sinus Dural Arteriovenous Fistula.","authors":"Yuwa Oka, Kenichi Komatsu, Soichiro Abe, Naoya Yoshimoto, Junya Taki, Sadayuki Matsumoto","doi":"10.1155/2020/2630959","DOIUrl":null,"url":null,"abstract":"<p><p>Symptoms of cavernous sinus dural arteriovenous fistula depend on the drainage patterns and are very diverse. Among these, brainstem dysfunction is a rare but serious complication. Here, we describe a case with isolated and rapidly progressive brainstem dysfunction due to cavernous sinus dural arteriovenous fistula. An 80-year-old woman presented with a 2-day history of progressive gait disturbance. Neurological examination revealed mild confusion, dysarthria, and left hemiparesis. Magnetic resonance imaging (MRI) revealed pontine swelling without evidence of infarction. Magnetic resonance angiography suggested a faint abnormality near the cavernous sinus. Dural arteriovenous fistula was suspected, and digital subtraction angiography was planned for the next day. Her condition had progressed to coma by the next morning. Pontine swelling worsened, and hyperintensity appeared on diffusion-weighted imaging. Digital subtraction angiography revealed a right-sided cavernous sinus dural arteriovenous fistula with venous reflux into the posterior fossa. Orbital or ocular symptoms had preceded brainstem symptoms in all nine previously reported cases, but brainstem symptoms were the only presentation in our case, making the diagnosis difficult. Some dural arteriovenous fistulas mimic inflammatory diseases when the clinical course is acute. Prompt diagnosis using enhanced computed tomography or MRI and emergent treatment are needed to avoid permanent sequelae.</p>","PeriodicalId":9615,"journal":{"name":"Case Reports in Neurological Medicine","volume":"2020 ","pages":"2630959"},"PeriodicalIF":0.9000,"publicationDate":"2020-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271059/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Neurological Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2020/2630959","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Symptoms of cavernous sinus dural arteriovenous fistula depend on the drainage patterns and are very diverse. Among these, brainstem dysfunction is a rare but serious complication. Here, we describe a case with isolated and rapidly progressive brainstem dysfunction due to cavernous sinus dural arteriovenous fistula. An 80-year-old woman presented with a 2-day history of progressive gait disturbance. Neurological examination revealed mild confusion, dysarthria, and left hemiparesis. Magnetic resonance imaging (MRI) revealed pontine swelling without evidence of infarction. Magnetic resonance angiography suggested a faint abnormality near the cavernous sinus. Dural arteriovenous fistula was suspected, and digital subtraction angiography was planned for the next day. Her condition had progressed to coma by the next morning. Pontine swelling worsened, and hyperintensity appeared on diffusion-weighted imaging. Digital subtraction angiography revealed a right-sided cavernous sinus dural arteriovenous fistula with venous reflux into the posterior fossa. Orbital or ocular symptoms had preceded brainstem symptoms in all nine previously reported cases, but brainstem symptoms were the only presentation in our case, making the diagnosis difficult. Some dural arteriovenous fistulas mimic inflammatory diseases when the clinical course is acute. Prompt diagnosis using enhanced computed tomography or MRI and emergent treatment are needed to avoid permanent sequelae.

Abstract Image

Abstract Image

海绵窦硬脑膜动静脉瘘引起的急性脑干功能障碍
海绵窦硬脑膜动静脉瘘的症状取决于引流方式,且多种多样。其中,脑干功能障碍是一种罕见但严重的并发症。在此,我们描述了一例因海绵窦硬脑膜动静脉瘘而导致的孤立且快速进展的脑干功能障碍。一名 80 岁的妇女因渐进性步态障碍就诊 2 天。神经系统检查发现她有轻度意识模糊、构音障碍和左侧偏瘫。磁共振成像(MRI)显示桥脑肿胀,但无梗死迹象。磁共振血管造影显示海绵窦附近有微弱异常。怀疑是硬脑膜动静脉瘘,计划第二天进行数字减影血管造影。第二天早上,她的病情发展到昏迷。桥脑肿胀加剧,弥散加权成像出现高密度。数字减影血管造影显示她右侧海绵窦硬膜动静脉瘘,静脉回流至后窝。在之前报道的九例病例中,眼眶或眼部症状均先于脑干症状出现,但在我们的病例中,脑干症状是唯一的表现,这给诊断带来了困难。一些硬脑膜动静脉瘘在临床病程较急时,会模仿炎症性疾病。需要使用增强型计算机断层扫描或核磁共振成像进行及时诊断和紧急治疗,以避免留下永久性后遗症。
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 求助全文
来源期刊
自引率
0.00%
发文量
26
审稿时长
11 weeks
×
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