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Anomalous origin of right pulmonary artery: diagnosis, treatment, and follow-up in an adult patient

Published online by Cambridge University Press:  06 July 2020

Susan Pumacayo-Cárdenas Open the ORCID record for Susan Pumacayo-Cárdenas [Opens in a new window] ,
Moises Jimenez-Santos  and
Edgar Quea-Pinto
Susan Pumacayo-Cárdenas*
Affiliation:
Departamento de Tomografía cardiaca, Instituto nacional de cardiología Ignacio Chávez, Ciudad de México, México
Moises Jimenez-Santos
Affiliation:
Departamento de Tomografía cardiaca, Instituto nacional de cardiología Ignacio Chávez, Ciudad de México, México
Edgar Quea-Pinto
Affiliation:
Departamento de cardiología intervencionista de cardiopatías congénitas, Instituto nacional de cardiología Ignacio Chávez, Ciudad de México, México
*
Author for correspondence: Susan Pumacayo-Cárdenas, Belisario Domínguez Sección 16, Belisario Domínguez Secc 16, Tlalpan, CDMX. Tel: +51979791469. E-mail: [email protected]
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Abstract

Anomalous origin of a branch pulmonary artery from the aorta is a rare malformation, accounting for 0.12% of all congenital heart defects. We present the case of a 43-year-old man with an anomalous origin of the right pulmonary artery (AORPA) from the ascending aorta. Reimplantation of the right pulmonary artery was carried out successfully, with favourable evolution in the medium-term follow-up. It is the first described case that receives corrective treatment in adulthood with a favourable evolution.

Keywords

anomalous origin of one pulmonary arterycongenital heart diseasecomputed tomographycardiac catheterisation
Type
Brief Report
Information
Cardiology in the Young , Volume 30 , Issue 8 , August 2020 , pp. 1199 - 1201
Copyright
© The Author(s), 2020. Published by Cambridge University Press

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