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A rare case of common arterial trunk with coarctation of the aorta: a case report

BACKGROUND: A common arterial trunk is a relatively uncommon type of congenital heart defect. The anomaly is caused by an incomplete conotruncal septation. Arch anomalies, such as interruption, are associated with 10–20% of cases. We present a rare case of common arterial trunk with coarctation of t...

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Autores principales: Abdelaal, Mohamed, Dedieu, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9278339/
https://www.ncbi.nlm.nih.gov/pubmed/35854881
http://dx.doi.org/10.1093/ehjcr/ytac257
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author Abdelaal, Mohamed
Dedieu, Nathalie
author_facet Abdelaal, Mohamed
Dedieu, Nathalie
author_sort Abdelaal, Mohamed
collection PubMed
description BACKGROUND: A common arterial trunk is a relatively uncommon type of congenital heart defect. The anomaly is caused by an incomplete conotruncal septation. Arch anomalies, such as interruption, are associated with 10–20% of cases. We present a rare case of common arterial trunk with coarctation of the aorta and patent ductus arteriosus (PDA). CASE SUMMARY: A term baby who was discovered to have a murmur on examination, for evaluation of the murmur an echocardiography was performed on Day 2 of life, which revealed the diagnosis of a common arterial trunk and coarctation of the aorta. The baby was given prostaglandin and intubated. Due to his poor general condition, he underwent an emergency pulmonary artery branch banding. He needed another 5 days in the intensive care unit to be stabilized before undergoing full repair. DISCUSSION: Our patient has a common arterial trunk with a tricuspid competent truncal valve. The trunk is subdivided further into ascending aorta and main pulmonary artery. The pulmonary artery provided two branches and a PDA that connected to the descending aorta. The aortic branching pattern was as usual, there was an area of tight coarctation and posterior shelf just after the origin of the left subclavian artery before the descending aorta–PDA junction. The presence of coarctation may be considered as the left side of the spectrum of morphological changes toward the formation of aortic arch interruption (Type 4 Van Praagh).
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spelling pubmed-92783392022-07-18 A rare case of common arterial trunk with coarctation of the aorta: a case report Abdelaal, Mohamed Dedieu, Nathalie Eur Heart J Case Rep Case Report BACKGROUND: A common arterial trunk is a relatively uncommon type of congenital heart defect. The anomaly is caused by an incomplete conotruncal septation. Arch anomalies, such as interruption, are associated with 10–20% of cases. We present a rare case of common arterial trunk with coarctation of the aorta and patent ductus arteriosus (PDA). CASE SUMMARY: A term baby who was discovered to have a murmur on examination, for evaluation of the murmur an echocardiography was performed on Day 2 of life, which revealed the diagnosis of a common arterial trunk and coarctation of the aorta. The baby was given prostaglandin and intubated. Due to his poor general condition, he underwent an emergency pulmonary artery branch banding. He needed another 5 days in the intensive care unit to be stabilized before undergoing full repair. DISCUSSION: Our patient has a common arterial trunk with a tricuspid competent truncal valve. The trunk is subdivided further into ascending aorta and main pulmonary artery. The pulmonary artery provided two branches and a PDA that connected to the descending aorta. The aortic branching pattern was as usual, there was an area of tight coarctation and posterior shelf just after the origin of the left subclavian artery before the descending aorta–PDA junction. The presence of coarctation may be considered as the left side of the spectrum of morphological changes toward the formation of aortic arch interruption (Type 4 Van Praagh). Oxford University Press 2022-06-28 /pmc/articles/PMC9278339/ /pubmed/35854881 http://dx.doi.org/10.1093/ehjcr/ytac257 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Abdelaal, Mohamed
Dedieu, Nathalie
A rare case of common arterial trunk with coarctation of the aorta: a case report
title A rare case of common arterial trunk with coarctation of the aorta: a case report
title_full A rare case of common arterial trunk with coarctation of the aorta: a case report
title_fullStr A rare case of common arterial trunk with coarctation of the aorta: a case report
title_full_unstemmed A rare case of common arterial trunk with coarctation of the aorta: a case report
title_short A rare case of common arterial trunk with coarctation of the aorta: a case report
title_sort rare case of common arterial trunk with coarctation of the aorta: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9278339/
https://www.ncbi.nlm.nih.gov/pubmed/35854881
http://dx.doi.org/10.1093/ehjcr/ytac257
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