Double Outlet Right Ventricle: A Rare Finding in a 15‐Month‐Old Female With Failure to Thrive

ABSTRACT Double outlet right ventricle (DORV) is a rare congenital heart defect where both the aorta and pulmonary artery originate from the right ventricle, often accompanied by additional cardiac anomalies to mitigate circulatory imbalance, though such compensations usually fail. We report a 15‐mo...

Full description

Saved in:
Bibliographic Details
Main Authors: Bernadette Pedun, Ivaan Pitua, Felix Bongomin, Samuel Bugeza, Rita Nassanga Luzinda
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Clinical Case Reports
Subjects:
Online Access:https://doi.org/10.1002/ccr3.70076
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832589896101920768
author Bernadette Pedun
Ivaan Pitua
Felix Bongomin
Samuel Bugeza
Rita Nassanga Luzinda
author_facet Bernadette Pedun
Ivaan Pitua
Felix Bongomin
Samuel Bugeza
Rita Nassanga Luzinda
author_sort Bernadette Pedun
collection DOAJ
description ABSTRACT Double outlet right ventricle (DORV) is a rare congenital heart defect where both the aorta and pulmonary artery originate from the right ventricle, often accompanied by additional cardiac anomalies to mitigate circulatory imbalance, though such compensations usually fail. We report a 15‐month‐old infant with recurrent respiratory infections and poor weight gain, referred for computed tomography angiography. Physical examination showed a small, non‐syndromic infant with pallor, tachypnea, irritability, and finger clubbing. Initial imaging revealed cardiomegaly and lung infiltrates; echocardiography and computed tomography angiography confirmed additional intracardiac defects of double superior vena cavae, a hypoplastic aortic arch, hypertrophic right ventricular wall, and a patent ductus arteriosus. Corrective surgery was delayed due to respiratory complications. This case emphasizes the critical need to consider cardiac pathology in pediatric patients with recurrent respiratory symptoms, as untreated DORV can lead to high mortality.
format Article
id doaj-art-3043707ae8634d488a77f0c1228df97b
institution Kabale University
issn 2050-0904
language English
publishDate 2025-01-01
publisher Wiley
record_format Article
series Clinical Case Reports
spelling doaj-art-3043707ae8634d488a77f0c1228df97b2025-01-24T05:08:46ZengWileyClinical Case Reports2050-09042025-01-01131n/an/a10.1002/ccr3.70076Double Outlet Right Ventricle: A Rare Finding in a 15‐Month‐Old Female With Failure to ThriveBernadette Pedun0Ivaan Pitua1Felix Bongomin2Samuel Bugeza3Rita Nassanga Luzinda4Uganda Cancer Institute Kampala UgandaSchool of Medicine, College of Health Sciences Makerere University Kampala UgandaDepartment of Internal Medicine Gulu Regional Referral Hospital Gulu UgandaDepartment of Radiology and Radiotherapy, School of Medicine, College of Health Sciences Makerere University Kampala UgandaDepartment of Radiology and Radiotherapy, School of Medicine, College of Health Sciences Makerere University Kampala UgandaABSTRACT Double outlet right ventricle (DORV) is a rare congenital heart defect where both the aorta and pulmonary artery originate from the right ventricle, often accompanied by additional cardiac anomalies to mitigate circulatory imbalance, though such compensations usually fail. We report a 15‐month‐old infant with recurrent respiratory infections and poor weight gain, referred for computed tomography angiography. Physical examination showed a small, non‐syndromic infant with pallor, tachypnea, irritability, and finger clubbing. Initial imaging revealed cardiomegaly and lung infiltrates; echocardiography and computed tomography angiography confirmed additional intracardiac defects of double superior vena cavae, a hypoplastic aortic arch, hypertrophic right ventricular wall, and a patent ductus arteriosus. Corrective surgery was delayed due to respiratory complications. This case emphasizes the critical need to consider cardiac pathology in pediatric patients with recurrent respiratory symptoms, as untreated DORV can lead to high mortality.https://doi.org/10.1002/ccr3.70076cardiac computed tomographycase reportcongenital heart defectdouble outlet right ventricleechocardiography
spellingShingle Bernadette Pedun
Ivaan Pitua
Felix Bongomin
Samuel Bugeza
Rita Nassanga Luzinda
Double Outlet Right Ventricle: A Rare Finding in a 15‐Month‐Old Female With Failure to Thrive
Clinical Case Reports
cardiac computed tomography
case report
congenital heart defect
double outlet right ventricle
echocardiography
title Double Outlet Right Ventricle: A Rare Finding in a 15‐Month‐Old Female With Failure to Thrive
title_full Double Outlet Right Ventricle: A Rare Finding in a 15‐Month‐Old Female With Failure to Thrive
title_fullStr Double Outlet Right Ventricle: A Rare Finding in a 15‐Month‐Old Female With Failure to Thrive
title_full_unstemmed Double Outlet Right Ventricle: A Rare Finding in a 15‐Month‐Old Female With Failure to Thrive
title_short Double Outlet Right Ventricle: A Rare Finding in a 15‐Month‐Old Female With Failure to Thrive
title_sort double outlet right ventricle a rare finding in a 15 month old female with failure to thrive
topic cardiac computed tomography
case report
congenital heart defect
double outlet right ventricle
echocardiography
url https://doi.org/10.1002/ccr3.70076
work_keys_str_mv AT bernadettepedun doubleoutletrightventricleararefindingina15montholdfemalewithfailuretothrive
AT ivaanpitua doubleoutletrightventricleararefindingina15montholdfemalewithfailuretothrive
AT felixbongomin doubleoutletrightventricleararefindingina15montholdfemalewithfailuretothrive
AT samuelbugeza doubleoutletrightventricleararefindingina15montholdfemalewithfailuretothrive
AT ritanassangaluzinda doubleoutletrightventricleararefindingina15montholdfemalewithfailuretothrive