Affiliations 

  • 1 Department of Cardiothoracic Surgery, National Heart Institute, Kuala Lumpur, Malaysia
Interact Cardiovasc Thorac Surg, 2020 10 01;31(4):576-577.
PMID: 32772077 DOI: 10.1093/icvts/ivaa126

Abstract

Berry syndrome is a rare congenital cardiac lesion consisting of a distal aortopulmonary window, the aortic origin of the right pulmonary artery (PA), intact ventricular septum and an interrupted or hypoplastic aortic arch. Different repair techniques have been described in the literature. We report a case of Berry syndrome, in whom myocardial ischaemia developed following direct implantation of the right PA to the main PA, which was resolved using an interposition tube graft.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.