Unobstructed infracardiac total anomalous pulmonary venous connection in a 7‐month‐old infant: A rare case report

Key Clinical Message This case underscores the importance of early detection and treatment for total anomalous pulmonary venous connection, a rare congenital heart condition, through comprehensive newborn physical exams and prompt specialist referrals. Abstract Total anomalous pulmonary venous conne...

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Main Authors: Eman Shhada, Ali Alakbar Nahle, Hussein Hamdar, Ali Jawad, Hasan Hasan, Mohammad Shadi Hamra, Mohannad Saleh, Alwaleed Al‐dairy, Huda Daood
Format: Article
Language:English
Published: Wiley 2023-10-01
Series:Clinical Case Reports
Subjects:
Online Access:https://doi.org/10.1002/ccr3.8079
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author Eman Shhada
Ali Alakbar Nahle
Hussein Hamdar
Ali Jawad
Hasan Hasan
Mohammad Shadi Hamra
Mohannad Saleh
Alwaleed Al‐dairy
Huda Daood
author_facet Eman Shhada
Ali Alakbar Nahle
Hussein Hamdar
Ali Jawad
Hasan Hasan
Mohammad Shadi Hamra
Mohannad Saleh
Alwaleed Al‐dairy
Huda Daood
author_sort Eman Shhada
collection DOAJ
description Key Clinical Message This case underscores the importance of early detection and treatment for total anomalous pulmonary venous connection, a rare congenital heart condition, through comprehensive newborn physical exams and prompt specialist referrals. Abstract Total anomalous pulmonary venous connection (TAPVC) is a rare form of congenital heart disease that is typically diagnosed in neonates. TAPVC has four subtypes, with the infracardiac type at risk of obstruction. TAPVC is usually diagnosed in newborns but can occur in other age groups. In this case, a 7‐month‐old male with recurrent cyanotic episodes was diagnosed with TAPVC of the infracardiac type using computed tomography angiography. The patient underwent successful surgical repair with a favorable postoperative course and was discharged in stable condition, and further follow‐up was not possible beyond 2 months. This case emphasizes the importance of early recognition and management of this condition to prevent the progression of subsequent complications.
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spelling doaj.art-b807092f21db49f584adc4331f54155e2023-10-25T07:12:45ZengWileyClinical Case Reports2050-09042023-10-011110n/an/a10.1002/ccr3.8079Unobstructed infracardiac total anomalous pulmonary venous connection in a 7‐month‐old infant: A rare case reportEman Shhada0Ali Alakbar Nahle1Hussein Hamdar2Ali Jawad3Hasan Hasan4Mohammad Shadi Hamra5Mohannad Saleh6Alwaleed Al‐dairy7Huda Daood8Pediatric Intensive Care Department, Faculty of Medicine, Children's Hospital Damascus University Damascus SyriaFaculty of Medicine Damascus University Damascus SyriaFaculty of Medicine Damascus University Damascus SyriaFaculty of Medicine Damascus University Damascus SyriaDepartment of Cardiac Surgery, Faculty of Medicine, Pediatric Cardiac Surgery Unit Damascus University Damascus SyriaDepartment of Cardiac Surgery, Faculty of Medicine, Pediatric Cardiac Surgery Unit Damascus University Damascus SyriaDepartment of Cardiac Surgery, Faculty of Medicine, Pediatric Cardiac Surgery Unit Damascus University Damascus SyriaDepartment of Cardiac Surgery, Faculty of Medicine, Pediatric Cardiac Surgery Unit Damascus University Damascus SyriaPediatric Intensive Care Department, Faculty of Medicine, Children's Hospital Damascus University Damascus SyriaKey Clinical Message This case underscores the importance of early detection and treatment for total anomalous pulmonary venous connection, a rare congenital heart condition, through comprehensive newborn physical exams and prompt specialist referrals. Abstract Total anomalous pulmonary venous connection (TAPVC) is a rare form of congenital heart disease that is typically diagnosed in neonates. TAPVC has four subtypes, with the infracardiac type at risk of obstruction. TAPVC is usually diagnosed in newborns but can occur in other age groups. In this case, a 7‐month‐old male with recurrent cyanotic episodes was diagnosed with TAPVC of the infracardiac type using computed tomography angiography. The patient underwent successful surgical repair with a favorable postoperative course and was discharged in stable condition, and further follow‐up was not possible beyond 2 months. This case emphasizes the importance of early recognition and management of this condition to prevent the progression of subsequent complications.https://doi.org/10.1002/ccr3.8079congenital heart diseaseechocardiography—case reportinfracardiactotal anomalous pulmonary venous connection
spellingShingle Eman Shhada
Ali Alakbar Nahle
Hussein Hamdar
Ali Jawad
Hasan Hasan
Mohammad Shadi Hamra
Mohannad Saleh
Alwaleed Al‐dairy
Huda Daood
Unobstructed infracardiac total anomalous pulmonary venous connection in a 7‐month‐old infant: A rare case report
Clinical Case Reports
congenital heart disease
echocardiography—case report
infracardiac
total anomalous pulmonary venous connection
title Unobstructed infracardiac total anomalous pulmonary venous connection in a 7‐month‐old infant: A rare case report
title_full Unobstructed infracardiac total anomalous pulmonary venous connection in a 7‐month‐old infant: A rare case report
title_fullStr Unobstructed infracardiac total anomalous pulmonary venous connection in a 7‐month‐old infant: A rare case report
title_full_unstemmed Unobstructed infracardiac total anomalous pulmonary venous connection in a 7‐month‐old infant: A rare case report
title_short Unobstructed infracardiac total anomalous pulmonary venous connection in a 7‐month‐old infant: A rare case report
title_sort unobstructed infracardiac total anomalous pulmonary venous connection in a 7 month old infant a rare case report
topic congenital heart disease
echocardiography—case report
infracardiac
total anomalous pulmonary venous connection
url https://doi.org/10.1002/ccr3.8079
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