硬脑膜窦畸形伴持续性幕前窦:罕见的变异。

IF 1.6 4区 医学 Q3 CLINICAL NEUROLOGY
Rebeca Santos, Sarah Wing, Mesha Martinez
{"title":"硬脑膜窦畸形伴持续性幕前窦:罕见的变异。","authors":"Rebeca Santos, Sarah Wing, Mesha Martinez","doi":"10.1177/08830738251376737","DOIUrl":null,"url":null,"abstract":"<p><p>This case report details a patient born with dural sinus malformation of the transtentorial sinus complicated by thrombosis, which caused compression of the fourth ventricle, venous infarction of the adjacent cerebellum, and disseminated intravascular coagulation. The enlarged, malformed pouch involved a transtentorial venous sinus, a sinus located in the tentorium cerebelli along the inner surface of the occipital bone that usually regresses before birth. The diagnosis was missed because of the rare presentation of a rare disease. In this case review, a multidisciplinary approach resulted in life-altering outcomes, with the patient meeting developmental milestones and exceeding expectations.</p>","PeriodicalId":15319,"journal":{"name":"Journal of Child Neurology","volume":" ","pages":"8830738251376737"},"PeriodicalIF":1.6000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dural Sinus Malformation Involving a Persistent Transtentorial Sinus: A Rare Variant.\",\"authors\":\"Rebeca Santos, Sarah Wing, Mesha Martinez\",\"doi\":\"10.1177/08830738251376737\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This case report details a patient born with dural sinus malformation of the transtentorial sinus complicated by thrombosis, which caused compression of the fourth ventricle, venous infarction of the adjacent cerebellum, and disseminated intravascular coagulation. The enlarged, malformed pouch involved a transtentorial venous sinus, a sinus located in the tentorium cerebelli along the inner surface of the occipital bone that usually regresses before birth. The diagnosis was missed because of the rare presentation of a rare disease. In this case review, a multidisciplinary approach resulted in life-altering outcomes, with the patient meeting developmental milestones and exceeding expectations.</p>\",\"PeriodicalId\":15319,\"journal\":{\"name\":\"Journal of Child Neurology\",\"volume\":\" \",\"pages\":\"8830738251376737\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-09-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Child Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/08830738251376737\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Child Neurology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/08830738251376737","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

本病例报告详细介绍了一例先天性小脑幕窦硬脑膜窦畸形并发血栓形成的病例,该畸形导致第四脑室受压,邻近小脑静脉梗死,弥散性血管内凝血。增大的畸形眼袋包括一个经小脑幕静脉窦,一个位于小脑幕沿枕骨内表面的窦,通常在出生前消退。由于一种罕见疾病的罕见表现而错过了诊断。在这个病例回顾中,多学科的方法导致了改变生活的结果,患者达到了发展里程碑并超出了期望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dural Sinus Malformation Involving a Persistent Transtentorial Sinus: A Rare Variant.

This case report details a patient born with dural sinus malformation of the transtentorial sinus complicated by thrombosis, which caused compression of the fourth ventricle, venous infarction of the adjacent cerebellum, and disseminated intravascular coagulation. The enlarged, malformed pouch involved a transtentorial venous sinus, a sinus located in the tentorium cerebelli along the inner surface of the occipital bone that usually regresses before birth. The diagnosis was missed because of the rare presentation of a rare disease. In this case review, a multidisciplinary approach resulted in life-altering outcomes, with the patient meeting developmental milestones and exceeding 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
Journal of Child Neurology
Journal of Child Neurology 医学-临床神经学
CiteScore
4.20
自引率
5.30%
发文量
111
审稿时长
3-6 weeks
期刊介绍: The Journal of Child Neurology (JCN) embraces peer-reviewed clinical and investigative studies from a wide-variety of neuroscience disciplines. Focusing on the needs of neurologic patients from birth to age 18 years, JCN covers topics ranging from assessment of new and changing therapies and procedures; diagnosis, evaluation, and management of neurologic, neuropsychiatric, and neurodevelopmental disorders; and pathophysiology of central nervous system diseases.
×
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:604180095
Book学术官方微信