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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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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). |
format | Online Article Text |
id | pubmed-9278339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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