• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

伴有弯刀综合征的持续性原始肝静脉丛:一例病例报告及文献复习

Persistent primitive hepatic venous plexus with Scimitar syndrome: description of a case and review of the literature.

作者信息

Restrepo M Santiago, Aldoss Osamah, Ng Benton

机构信息

Department of Pediatrics,Division of Pediatric Cardiology,University of Iowa Children's Hospital,Carver College of Medicine,Iowa City,Iowa,United States of America.

出版信息

Cardiol Young. 2015 Jun;25(5):1009-11. doi: 10.1017/S1047951114001498. Epub 2014 Sep 24.

DOI:10.1017/S1047951114001498
PMID:25249237
Abstract

Persistent primitive hepatic venous plexus is an anomaly of the systemic venous return characterised by postnatal persistence of the foetal intrahepatic venous drainage. Scimitar syndrome is a condition that consists of partial anomalous pulmonary venous return of the right pulmonary venous drainage into the systemic veins, associated with pulmonary artery hypoplasia with the underdeveloped right lung, pulmonary sequestration, and cardiac malposition. Both conditions are rare and together have been rarely described in the literature. We report the first case of this combination of lesions imaged by cardiac magnetic resonance imaging with a three-dimensional reconstruction and reviewed the literature to characterise this uncommon combination.

摘要

持续性原始肝静脉丛是一种体循环静脉回流异常,其特征为胎儿期肝内静脉引流在出生后持续存在。弯刀综合征是一种由右肺静脉引流部分异常肺静脉回流至体静脉、伴有右肺发育不全的肺动脉发育不全、肺隔离症和心脏异位组成的疾病。这两种情况都很罕见,且在文献中很少一起描述。我们报告了首例通过心脏磁共振成像及三维重建对这种联合病变进行成像的病例,并回顾了文献以描述这种罕见的联合情况。

相似文献

1
Persistent primitive hepatic venous plexus with Scimitar syndrome: description of a case and review of the literature.伴有弯刀综合征的持续性原始肝静脉丛:一例病例报告及文献复习
Cardiol Young. 2015 Jun;25(5):1009-11. doi: 10.1017/S1047951114001498. Epub 2014 Sep 24.
2
Scimitar syndrome associated with absence of the right pulmonary artery and a persistent primitive hepatic venous plexus.
Cardiol Young. 2005 Apr;15(2):216-8. doi: 10.1017/S1047951105000429.
3
Scimitar syndrome.弯刀综合征
Arch Iran Med. 2009 Jan;12(1):79-81.
4
Double venous drainage in scimitar syndrome. Ideal anatomy for percutaneous complete cure.弯刀综合征中的双静脉引流。经皮完全治愈的理想解剖结构。
Cardiol Young. 2011 Jun;21(3):357-60. doi: 10.1017/S1047951111000096. Epub 2011 Feb 4.
5
[Anomalous pulmonary venous return in a pregnant woman identified by cardiac magnetic resonance].[通过心脏磁共振成像确诊的孕妇异常肺静脉回流]
Rev Port Cardiol. 2014 Jun;33(6):383.e1-5. doi: 10.1016/j.repc.2014.02.009. Epub 2014 Jul 4.
6
Meandering pulmonary veins mimicking scimitar syndrome.迂曲的肺静脉酷似弯刀综合征。
Cardiol Young. 2018 Oct;28(10):1171-1173. doi: 10.1017/S1047951118001117. Epub 2018 Jul 11.
7
Unusual variant of a rare constellation: a left-sided scimitar syndrome with connection to the azygos vein.一种罕见综合征的不寻常变异:左侧弯刀综合征伴奇静脉连接。
Congenit Heart Dis. 2010 Mar-Apr;5(2):174-7. doi: 10.1111/j.1747-0803.2010.00401.x.
8
Rare case of undiagnosed supracardiac total anomalous pulmonary venous return in an adult.成人未确诊的心上型完全性肺静脉异位引流罕见病例。
Circulation. 2014 Sep 30;130(14):1205-7. doi: 10.1161/CIRCULATIONAHA.114.008013.
9
Persistent primitive hepatic venous plexus in a child with scimitar syndrome.一名患有弯刀综合征儿童的持续性原始肝静脉丛
Int J Cardiol. 2011 Sep 15;151(3):e88-9. doi: 10.1016/j.ijcard.2010.06.002. Epub 2010 Jun 26.
10
[Combination of scimitar syndrome and horseshoe lung. A rare but typical finding--case report and review of the literature].[弯刀综合征合并马蹄肺。一种罕见但典型的表现——病例报告及文献复习]
Klin Padiatr. 1992 Nov-Dec;204(6):434-43. doi: 10.1055/s-2007-1025385.

引用本文的文献

1
An ATX-LPA-Gα-ROCK axis shapes and maintains caudal vein plexus in zebrafish.一种自分泌运动因子-溶血磷脂酸-Gα- Rho相关卷曲螺旋蛋白激酶轴塑造并维持斑马鱼的尾静脉丛。
iScience. 2021 Oct 12;24(11):103254. doi: 10.1016/j.isci.2021.103254. eCollection 2021 Nov 19.