Fallot type of absent pulmonary valve syndrome - A case report

Absent pulmonary valve syndrome (APVS) is a rare congenital cardiac malformation characterized by absent, dysplastic, or rudimentary pulmonary valve leaflets in association with other cardiac anomalies. It has an incidence of 3-6% in cases of tetralogy of Fallot (TOF) and 0.2-0.4% of live-born infan...

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Autores principales: Desai, Divya B, Mathur, Neeti P, Marik, Arnab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546300/
https://www.ncbi.nlm.nih.gov/pubmed/33100698
http://dx.doi.org/10.4103/ijri.IJRI_508_19
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author Desai, Divya B
Mathur, Neeti P
Marik, Arnab
author_facet Desai, Divya B
Mathur, Neeti P
Marik, Arnab
author_sort Desai, Divya B
collection PubMed
description Absent pulmonary valve syndrome (APVS) is a rare congenital cardiac malformation characterized by absent, dysplastic, or rudimentary pulmonary valve leaflets in association with other cardiac anomalies. It has an incidence of 3-6% in cases of tetralogy of Fallot (TOF) and 0.2-0.4% of live-born infants with congenital heart disease (CHD). Absent pulmonary valve leads to dilated main pulmonary artery; presenting as a pulsatile, paracardiac cystic lesion on antenatal ultrasound (USG). We report a case of this rare anomaly in association with ventricular septal defect (VSD), TOF, and left axis deviation of heart detected at 23 weeks of gestation.
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spelling pubmed-75463002020-10-22 Fallot type of absent pulmonary valve syndrome - A case report Desai, Divya B Mathur, Neeti P Marik, Arnab Indian J Radiol Imaging Case Report Absent pulmonary valve syndrome (APVS) is a rare congenital cardiac malformation characterized by absent, dysplastic, or rudimentary pulmonary valve leaflets in association with other cardiac anomalies. It has an incidence of 3-6% in cases of tetralogy of Fallot (TOF) and 0.2-0.4% of live-born infants with congenital heart disease (CHD). Absent pulmonary valve leads to dilated main pulmonary artery; presenting as a pulsatile, paracardiac cystic lesion on antenatal ultrasound (USG). We report a case of this rare anomaly in association with ventricular septal defect (VSD), TOF, and left axis deviation of heart detected at 23 weeks of gestation. Wolters Kluwer - Medknow 2020 2020-07-13 /pmc/articles/PMC7546300/ /pubmed/33100698 http://dx.doi.org/10.4103/ijri.IJRI_508_19 Text en Copyright: © 2020 Indian Journal of Radiology and Imaging http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Desai, Divya B
Mathur, Neeti P
Marik, Arnab
Fallot type of absent pulmonary valve syndrome - A case report
title Fallot type of absent pulmonary valve syndrome - A case report
title_full Fallot type of absent pulmonary valve syndrome - A case report
title_fullStr Fallot type of absent pulmonary valve syndrome - A case report
title_full_unstemmed Fallot type of absent pulmonary valve syndrome - A case report
title_short Fallot type of absent pulmonary valve syndrome - A case report
title_sort fallot type of absent pulmonary valve syndrome - a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546300/
https://www.ncbi.nlm.nih.gov/pubmed/33100698
http://dx.doi.org/10.4103/ijri.IJRI_508_19
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