Suppr超能文献

起源于右肺动脉的孤立性右颈总动脉。

Isolated Right Common Carotid Artery Arising from the Right Pulmonary Artery.

作者信息

Romberg Erin K, Schauer Jenna S, Cuffee Heidi, Yung Delphine, Ferguson Mark R

机构信息

Department of Radiology (E.K.R., M.R.F.) and Department of Pediatrics, Division of Cardiology (J.S.S., D.Y.), University of Washington and Seattle Children's Hospital, 4800 Sand Point Way NE, Seattle, WA 98105; and Department of Pediatric Cardiology, Seattle Children's Hospital, Seattle, Wash (H.C.).

出版信息

Radiol Cardiothorac Imaging. 2022 Oct 27;4(5):e220126. doi: 10.1148/ryct.220126. eCollection 2022 Oct.

Abstract

Isolated aortic arch vessels arising anomalously from the pulmonary arterial system are rare congenital anomalies. Case reports of isolated arch vessels are often associated with 22q11 deletion, CHARGE syndrome, or right aortic arch. Isolation of the carotid artery may lead to cerebral steal phenomenon and ischemia or to pulmonary overcirculation. The authors report what is, to their knowledge, the first case of isolated right common carotid artery arising from the right pulmonary artery, associated with 22q11 deletion, and describe the challenging multimodality image evaluation. Congenital, Anatomy, Carotid Arteries © RSNA, 2022.

摘要

孤立的主动脉弓血管异常起源于肺动脉系统是罕见的先天性异常。孤立弓血管的病例报告常与22q11缺失、CHARGE综合征或右主动脉弓相关。颈动脉孤立可能导致脑盗血现象和缺血或肺循环过度。据作者所知,本文报告了首例起源于右肺动脉的孤立右颈总动脉病例,该病例与22q11缺失相关,并描述了具有挑战性的多模态影像评估。先天性、解剖学、颈动脉 © RSNA,2022年。

相似文献

1
Isolated Right Common Carotid Artery Arising from the Right Pulmonary Artery.起源于右肺动脉的孤立性右颈总动脉。
Radiol Cardiothorac Imaging. 2022 Oct 27;4(5):e220126. doi: 10.1148/ryct.220126. eCollection 2022 Oct.
10

本文引用的文献

5
Congenital Variants and Anomalies of the Aortic Arch.主动脉弓的先天性变异与异常
Radiographics. 2017 Jan-Feb;37(1):32-51. doi: 10.1148/rg.2017160033. Epub 2016 Nov 18.

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