| Literature DB >> 20682530 |
Anne-Laure Verin1, Nicolas Creuze, Dominique Musset.
Abstract
Various malformations of the aortic arch and great vessels have been reported in the literature, which reflects the complexity of their embryologic development. Most of them are of incidental finding and remain asymptomatic but can be responsible for respiratory or digestive symptoms and be associated with congenital cardiac diseases. We report the case of a patient presenting a right retroesophageal vertebral artery. This malformation was associated with multiple anomalies of the aortic arch. We report a classification of the most common aortic arch abnormalities by recalling Edwards double aortic arch model and embryologic variants. Here, we report on the rare case of a right retroesophageal vertebral artery. We assimilate this malformation to a vertebral arteria lusoria and attribute it to the lack of caudal migration of the fourth branchial arch, responsible for a left cervical aortic arch with an interruption between the right subclavian and vertebral arteries.Entities:
Mesh:
Year: 2010 PMID: 20682530 DOI: 10.1378/chest.09-2244
Source DB: PubMed Journal: Chest ISSN: 0012-3692 Impact factor: 9.410