Romberg Erin K, Schauer Jenna S, Cuffee Heidi, Yung Delphine, Ferguson Mark R
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.).
Radiol Cardiothorac Imaging. 2022 Oct 27;4(5):e220126. doi: 10.1148/ryct.220126. eCollection 2022 Oct.
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.
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。