Moes C A, Freedom R M
Department of Radiology, Hospital for Sick Children, Toronto, Canada.
Pediatr Cardiol. 1993 Mar;14(2):93-101. doi: 10.1007/BF00796987.
Rare types of aortic arch malformations include isolation of the right or left subclavian arteries in conjunction with a left or right aortic arch respectively. Isolation of the innominate or carotid arteries and an aberrant left innominate artery may exist in association with a right aortic arch. Other anomalies are persistent fifth aortic arch, subclavian artery as the first branch of the aortic arch, pulmonary artery, and ductus arteriosus sling. The angiocardiographic features and embryology of each of these malformations are discussed.
罕见类型的主动脉弓畸形包括右或左锁骨下动脉孤立,分别与左或右主动脉弓相连。无名动脉或颈动脉孤立以及迷走左无名动脉可能与右主动脉弓并存。其他异常包括持续存在的第五主动脉弓、作为主动脉弓第一分支的锁骨下动脉、肺动脉和动脉导管吊带。本文讨论了这些畸形各自的心血管造影特征和胚胎学。