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Aortopulmonary window with anomalous right coronary artery from the pulmonary artery. Case report and literature review

Published online by Cambridge University Press:  19 December 2019

Ali A. Alakhfash Open the ORCID record for Ali A. Alakhfash [Opens in a new window] ,
Mohamad Tagelden ,
Abdulrahman Almesned  and
Abdullah Alqwaiee
Ali A. Alakhfash*
Affiliation:
Consultant Pediatric Cardiologist, Prince Sultan Cardiac Centre – Qassim, MOH, Kingdom of Saudi Arabia PhD Researcher, Sapienza University of Rome, Rome, Italy
Mohamad Tagelden
Affiliation:
Consultant Pediatric Cardiologist, Prince Sultan Cardiac Centre – Qassim, MOH, Kingdom of Saudi Arabia
Abdulrahman Almesned
Affiliation:
Consultant Pediatric Cardiologist, Prince Sultan Cardiac Centre – Qassim, MOH, Kingdom of Saudi Arabia
Abdullah Alqwaiee
Affiliation:
Consultant Pediatric Cardiologist, Prince Sultan Cardiac Centre – Qassim, MOH, Kingdom of Saudi Arabia
*
Author for correspondence: Ali A. Alakhfash, MD, Prince Sultan Cardiac Centre-Qassim, MOH, PO Box 896 51421, Saudi Arabia. Tel: (966)163827799; Fax: (966)163827799; E-mail: [email protected]
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Abstract

Aortopulmonary window is a rare congenital heart lesion. It might be associated with other CHDs, as well as with anomalous origin of the coronary arteries. Anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is the most commonly described coronary artery anomaly in association with aortopulmonary window. We are describing a premature neonate who was diagnosed to have aortopulmonary window and ARCAPA immediately after birth, and had a successful operation at the age of 4 months. This report highlights the importance of very careful assessment of the coronary arteries in patients with aortopulmonary window.

Keywords

CHDAortopulmonary windowAnomalous right coronary artery from pulmonary artery
Type
Original Article
Information
Cardiology in the Young , Volume 30 , Issue 1 , January 2020 , pp. 47 - 49
Copyright
© Cambridge University Press 2019

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References

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