| Literature DB >> 28260541 |
Ziyad M Binsalamah1, Peter Chen1, Emmett D McKenzie1.
Abstract
Persistence of the fifth aortic arch is a very rare anomaly, but is clinically relevant when it is associated with coarctation. We report a case of a neonate with type A interrupted aortic arch and severe coarctation of a persistent fifth aortic arch, which was discovered after repair of a left congenital diaphragmatic hernia. The combination of anomalies was discovered intra-operatively following left thoracotomy, and was treated with aortic arch advancement. The postoperative course was uneventful.Entities:
Keywords: Coarctation; aortic arch advancement; interrupted aortic arch; left thoracotomy; neonate
Mesh:
Year: 2017 PMID: 28260541 DOI: 10.1017/S1047951117000051
Source DB: PubMed Journal: Cardiol Young ISSN: 1047-9511 Impact factor: 1.093