新生儿盖伦静脉畸形:病例系列。

Erik F Hauck, Jeremy A Yarden, Lily I Hauck, Joseph M Bibawy, Shervin Mirshahi, Gerald A Grant
{"title":"新生儿盖伦静脉畸形:病例系列。","authors":"Erik F Hauck,&nbsp;Jeremy A Yarden,&nbsp;Lily I Hauck,&nbsp;Joseph M Bibawy,&nbsp;Shervin Mirshahi,&nbsp;Gerald A Grant","doi":"10.3171/CASE23201","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Vein of Galen malformations (VoGMs) in newborns often represent life-threatening emergencies. Outcome is difficult to predict. The authors review 50 VoGM cases to correlate anatomical types with treatment and outcome.</p><p><strong>Observations: </strong>Four distinct types of VoGMs are identified: mural simple (type I), mural complex (type II), choroidal (type III), and choroidal with deep venous drainage (type IV). Seven patients presented with mural simple VoGMs with a \"single hole\" fistula supplied by only one large feeder. These patients were treated electively at >6 months; development was normal. Fifteen patients presented with complex mural VoGMs. Multiple large feeders joined a single fistulous point within the wall of the varix. Patients typically presented with congestive heart failure (CHF) and required emergent transarterial intervention. Mortality was 7.7% with less than two-thirds developing normally. Twenty-five patients presented with choroidal VoGMs. Multiple large arterial feeders joined at multiple fistulous sites. Severe CHF in most patients required emergent transarterial and sometimes transvenous intervention. Mortality was 9.5%; two-thirds of the patients had a normal development. Three babies presented with choroidal VoGMs with deep intraventricular venous drainage. This phenomenon caused fatal \"melting brain syndrome\" in all three patients.</p><p><strong>Lessons: </strong>Recognition of the specific VoGM type determines treatment options and sets outcome expectations.</p>","PeriodicalId":16554,"journal":{"name":"Journal of Neurosurgery: Case Lessons","volume":"5 24","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/79/29/CASE23201.PMC10550657.pdf","citationCount":"0","resultStr":"{\"title\":\"Vein of Galen malformations in the newborn: case series.\",\"authors\":\"Erik F Hauck,&nbsp;Jeremy A Yarden,&nbsp;Lily I Hauck,&nbsp;Joseph M Bibawy,&nbsp;Shervin Mirshahi,&nbsp;Gerald A Grant\",\"doi\":\"10.3171/CASE23201\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Vein of Galen malformations (VoGMs) in newborns often represent life-threatening emergencies. Outcome is difficult to predict. The authors review 50 VoGM cases to correlate anatomical types with treatment and outcome.</p><p><strong>Observations: </strong>Four distinct types of VoGMs are identified: mural simple (type I), mural complex (type II), choroidal (type III), and choroidal with deep venous drainage (type IV). Seven patients presented with mural simple VoGMs with a \\\"single hole\\\" fistula supplied by only one large feeder. These patients were treated electively at >6 months; development was normal. Fifteen patients presented with complex mural VoGMs. Multiple large feeders joined a single fistulous point within the wall of the varix. Patients typically presented with congestive heart failure (CHF) and required emergent transarterial intervention. Mortality was 7.7% with less than two-thirds developing normally. Twenty-five patients presented with choroidal VoGMs. Multiple large arterial feeders joined at multiple fistulous sites. Severe CHF in most patients required emergent transarterial and sometimes transvenous intervention. Mortality was 9.5%; two-thirds of the patients had a normal development. Three babies presented with choroidal VoGMs with deep intraventricular venous drainage. This phenomenon caused fatal \\\"melting brain syndrome\\\" in all three patients.</p><p><strong>Lessons: </strong>Recognition of the specific VoGM type determines treatment options and sets outcome expectations.</p>\",\"PeriodicalId\":16554,\"journal\":{\"name\":\"Journal of Neurosurgery: Case Lessons\",\"volume\":\"5 24\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-06-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/79/29/CASE23201.PMC10550657.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Neurosurgery: Case Lessons\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3171/CASE23201\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neurosurgery: Case Lessons","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3171/CASE23201","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景:新生儿盖伦静脉畸形(VoGM)通常代表危及生命的紧急情况。结果很难预测。作者回顾了50例VoGM病例,以将解剖类型与治疗和结果相关联。观察结果:确定了四种不同类型的VoGM:附壁单纯型(I型)、附壁复合型(II型)、脉络膜型(III型)和脉络膜深静脉引流型(IV型)。7名患者出现了仅由一个大型喂食器供应的带有“单孔”瘘管的附壁简单VoGM。这些患者在>6个月时接受选择性治疗;发育正常。15名患者出现复杂的壁画VoGM。多个大型喂食器连接了静脉壁内的一个瘘管点。患者通常表现为充血性心力衰竭(CHF),需要紧急动脉介入治疗。死亡率为7.7%,正常发育的不到三分之二。25例患者出现脉络膜VoGM。多个大动脉供血器在多个瘘管部位连接。大多数严重CHF患者需要紧急经动脉介入治疗,有时需要经静脉介入治疗。死亡率为9.5%;三分之二的患者发育正常。三名婴儿出现脉络膜VoGMs,伴有脑室深静脉引流。这一现象导致三名患者出现致命的“脑融化综合征”。经验教训:对特定VoGM类型的认识决定了治疗选择并设定了结果预期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vein of Galen malformations in the newborn: case series.

Vein of Galen malformations in the newborn: case series.

Vein of Galen malformations in the newborn: case series.

Vein of Galen malformations in the newborn: case series.

Background: Vein of Galen malformations (VoGMs) in newborns often represent life-threatening emergencies. Outcome is difficult to predict. The authors review 50 VoGM cases to correlate anatomical types with treatment and outcome.

Observations: Four distinct types of VoGMs are identified: mural simple (type I), mural complex (type II), choroidal (type III), and choroidal with deep venous drainage (type IV). Seven patients presented with mural simple VoGMs with a "single hole" fistula supplied by only one large feeder. These patients were treated electively at >6 months; development was normal. Fifteen patients presented with complex mural VoGMs. Multiple large feeders joined a single fistulous point within the wall of the varix. Patients typically presented with congestive heart failure (CHF) and required emergent transarterial intervention. Mortality was 7.7% with less than two-thirds developing normally. Twenty-five patients presented with choroidal VoGMs. Multiple large arterial feeders joined at multiple fistulous sites. Severe CHF in most patients required emergent transarterial and sometimes transvenous intervention. Mortality was 9.5%; two-thirds of the patients had a normal development. Three babies presented with choroidal VoGMs with deep intraventricular venous drainage. This phenomenon caused fatal "melting brain syndrome" in all three patients.

Lessons: Recognition of the specific VoGM type determines treatment options and sets outcome expectations.

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