| Literature DB >> 17162395 |
Nazan Ozbarlas1, Sevcan Erdem, Osman Kucukosmanoglu, Hakan Poyrazoglu, Orhan Kemal Salih.
Abstract
Congenital aortico-cameral communications are rarely seen. We present an asymptomatic patient in whom there was a congenital vascular communication rising from the aortic root and terminating in the left atrium. She had an atrial septal defect (ASD). The diagnosis was made with echocardiography and confirmed by aortography. She was treated by closing the tunnel and the ASD. The outcome was satisfactory in this extremely rare case of a congenital cardiac lesion. Coincidental diagnosis could be made during careful echocardiographic examination.Entities:
Mesh:
Year: 2007 PMID: 17162395 DOI: 10.1532/HSF98.20061114
Source DB: PubMed Journal: Heart Surg Forum ISSN: 1098-3511 Impact factor: 0.676