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Aortopulmonary window with anomalous origin of the right coronary artery from the pulmonary trunk

Published online by Cambridge University Press:  11 January 2021

Atakan Atalay*
Affiliation:
Ankara City Hospital, Department of Pediatric Cardiovascular Surgery, Ankara, Turkey
Başak Soran Turkcan
Affiliation:
Ankara City Hospital, Department of Pediatric Cardiovascular Surgery, Ankara, Turkey
Emre Kulahcioglu
Affiliation:
Ankara City Hospital, Department of Pediatric Cardiovascular Surgery, Ankara, Turkey
Deniz Eris
Affiliation:
Isparta City Hospital, Department of Pediatric Cardiology, Isparta, Turkey
İbrahim Ece
Affiliation:
Ankara City Hospital, Department of Neonatology, Ankara, Turkey
Hakan Aydın
Affiliation:
Ankara City Hospital, Department of Pediatric Cardiovascular Surgery, Ankara, Turkey
*
Author for correspondence: Dr A. Atalay, MD, Ankara City Hospital, Üniversiteler Mah., Bilkent Blv. No:1, 06800 Çankaya/Ankara, Turkey. Tel: +90 5053 593 390; Fax: +90 312 552 60 00. E-mail: [email protected]

Abstract

Anomalous origin of coronary artery originating from the pulmonary artery in conjunction with the aorticopulmonary window (APW) is a rare but a significant anomaly in the era of congenital cardiac diseases. The occurrence of anomalous origin of the right coronary artery from the pulmonary artery among the associated anomalies is less than 5%. The severity of the clinical condition of these patients depends on the degree of left–right shunt and compromise of the pulmonary blood flow. We report surgical management of a case of a 45-day-old infant with APW, ventricular septal defect, and anomalous origin of coronary artery originated from the pulmonary artery.

Type
Brief Report
Copyright
© The Author(s), 2021. Published by Cambridge University Press

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