Coarctation of persistent right fifth aortic arch and pulmonary sequestration.
- 1 October 1998
- journal article
- case report
- Published by Cambridge University Press (CUP) in Cardiology in the Young
- Vol. 8 (4) , 509-511
- https://doi.org/10.1017/s1047951100007198
Abstract
A 41-day-old boy was transferred to our department with severe congestive heart failure. Digital subtraction counter current aortography, and antegrade aortography, revealed coarctation of a persistent right fifth aortic arch, stenosis of the origin of an aberrant left subclavian artery, and sequestration of the lower lobe of the right lung. As his heart failure seemed to be caused not only by pressure overload to the left ventricle following coarctation, but also by the volume load associated with the shunting effect of the pulmonary sequestration, we performed transcatheter balloon dilation of the coarctation and the origin of the aberrant subclavian artery, together with embolization of the aberrant pulmonary artery. His heart failure responded dramatically to these procedures.Keywords
This publication has 5 references indexed in Scilit:
- Percutaneous coil embolization of superfluous vascular connections in patients with congenital heart diseaseAmerican Heart Journal, 1993
- Intralobar Pulmonary Sequestration Presenting as Congestive Heart Failure in a NeonateChest, 1992
- Persistence of hypoplastic and recoarcted fifth aortic arch associated with type A aortic arch interruption: Surgical and balloon angioplasty results in an infantPediatric Cardiology, 1992
- Persistent left fifth aortic arch with complex coarctationThe American Journal of Cardiology, 1991
- Pulmonary Sequestration Causing Congestive Heart Failure in Infancy: A Report of Two Cases and Review of the LiteratureThe Annals of Thoracic Surgery, 1982