• 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

双主动脉弓作为儿童气道梗阻的一个原因。

Double aortic arch as a source of airway obstruction in a child.

作者信息

Das Sambhunath, Nair Vinitha V, Airan Balram

机构信息

Department of Cardiac Anaesthesia, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Ann Card Anaesth. 2015 Jan-Mar;18(1):111-2. doi: 10.4103/0971-9784.148336.

DOI:10.4103/0971-9784.148336
PMID:25566726
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4900311/
Abstract

Double aortic arch (DAA) is a congenital vascular anomaly. The diagnosis was difficult till the child was symptomatic, and other causes were ruled out. We present the interesting images of a child of respiratory distress because of tracheal compression from DAA.

摘要

双主动脉弓(DAA)是一种先天性血管异常。在患儿出现症状且排除其他病因之前,诊断较为困难。我们展示了一名因双主动脉弓压迫气管而出现呼吸窘迫的患儿的有趣影像。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ef/4900311/f8958fb33872/ACA-18-111-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ef/4900311/7f3c9319b9e5/ACA-18-111-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ef/4900311/ff54a4fce3b9/ACA-18-111-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ef/4900311/f8958fb33872/ACA-18-111-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ef/4900311/7f3c9319b9e5/ACA-18-111-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ef/4900311/ff54a4fce3b9/ACA-18-111-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ef/4900311/f8958fb33872/ACA-18-111-g003.jpg

相似文献

1
Double aortic arch as a source of airway obstruction in a child.双主动脉弓作为儿童气道梗阻的一个原因。
Ann Card Anaesth. 2015 Jan-Mar;18(1):111-2. doi: 10.4103/0971-9784.148336.
2
Distal tracheal stenosis in two children with double aortic arch and associated tracheomalacia.两名患有双主动脉弓及相关气管软化症的儿童出现远端气管狭窄。
Eur J Cardiothorac Surg. 1990;4(5):287-9. doi: 10.1016/1010-7940(90)90255-x.
3
Photoclinic. Central airway obstruction (CAO) due to right aortic arch anomaly.光诊所。右主动脉弓异常导致的中央气道梗阻(CAO)。
Arch Iran Med. 2013 Mar;16(3):197-8.
4
Vascular anomalies causing tracheoesophageal compression: a 20-year experience in diagnosis and management.导致气管食管受压的血管异常:20年诊断与治疗经验
Heart Surg Forum. 2003;6(3):149-52.
5
[Diagnosis and treatment of secondary tracheomalacia in intrathoracic compression of respiratory tracts caused by vascular ring anomaly in children].[小儿血管环异常致胸内呼吸道受压继发气管软化症的诊断与治疗]
Klin Khir. 2000(1):46-8.
6
Double aortic arch associated with tracheal and esophageal compression in an adult.成人双主动脉弓合并气管和食管受压
Anadolu Kardiyol Derg. 2014 Jun 9;14(5):E14-5. doi: 10.5152/akd.2014.5487.
7
Operation for aortic arch anomalies.主动脉弓畸形手术
Ann Thorac Surg. 1981 May;31(5):426-32. doi: 10.1016/s0003-4975(10)60994-0.
8
Right-sided aortic arch presenting as refractory intraoperative and postoperative wheezing.
Chest. 1991 May;99(5):1308-10. doi: 10.1378/chest.99.5.1308.
9
Aortic wheeze: intermittent tracheal obstruction caused by a rare aortic arch anomaly.主动脉喘鸣:一种由罕见的主动脉弓异常引起的间歇性气管阻塞。
Ann Otol Rhinol Laryngol. 1983 Jul-Aug;92(4 Pt 1):383-6. doi: 10.1177/000348948309200418.
10
Tracheal compression due to an elongated aortic arch in patients with congenital heart disease: evaluation using multidetector-row CT.先天性心脏病患者中主动脉弓延长导致的气管受压:使用多排探测器CT进行评估
Pediatr Radiol. 2009 Oct;39(10):1048-53. doi: 10.1007/s00247-009-1319-1. Epub 2009 Jun 23.

引用本文的文献

1
Double aortic arch: a rare cause of stridor in infants.双主动脉弓:婴儿喘鸣的罕见原因。
J Surg Case Rep. 2021 Dec 24;2021(12):rjab567. doi: 10.1093/jscr/rjab567. eCollection 2021 Dec.
2
Two cases of unusual airway pathology, in which a careful history contributed to a successful diagnosis.两例特殊气道病变病例,其中详细的病史有助于做出成功诊断。
Afr J Thorac Crit Care Med. 2018 Dec 20;24(4). doi: 10.7196/AJTCCM.2018.v24i4.221. eCollection 2018.
3
Undiagnosed Double Aortic Arch in an Adult With Repaired Tetralogy of Fallot.

本文引用的文献

1
Massive hemorrhage after Kasai portoenterostomy in a patient with a congenital extrahepatic portosystemic shunt, malrotation and a double aortic arch: report of a case.一名患有先天性肝外门体分流、肠旋转不良和双主动脉弓的患者在葛西肝门空肠吻合术后发生大出血:病例报告。
Surg Today. 2014 Aug;44(8):1561-4. doi: 10.1007/s00595-013-0605-6. Epub 2013 May 9.
2
Airway management in an infant with double aortic arch.婴儿双主动脉弓的气道管理。
J Anesth. 2010 Feb;24(1):117-20. doi: 10.1007/s00540-009-0850-4. Epub 2010 Jan 6.
3
Vascular ring: tracheoesophageal compression associated with symmetrical double aortic arch.
一名法洛四联症已修复的成年人中未被诊断出的双主动脉弓。
JACC Case Rep. 2019 Oct 30;1(4):540-544. doi: 10.1016/j.jaccas.2019.08.022. eCollection 2019 Dec.
4
The Management of Cyanotic Spells in Children with Oesophageal Atresia.食管闭锁患儿青紫发作的管理
Front Pediatr. 2017 May 15;5:106. doi: 10.3389/fped.2017.00106. eCollection 2017.
血管环:与对称性双主动脉弓相关的气管食管受压。
Tex Heart Inst J. 2008;35(2):209-10.