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Tetralogy of fallot in addition to anomalous aortic origin of a coronary artery in a 1-year-old boy: a case report
BACKGROUND: Anomalous aortic origin of a coronary artery (AAOCA) is a rare congenital heart disease, characterized by the coronary artery inappropriately originates from the aorta. It is usually classified according to the sinus where the coronary artery arises from, while anomalous origin of the ri...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557548/ https://www.ncbi.nlm.nih.gov/pubmed/34717598 http://dx.doi.org/10.1186/s12893-021-01380-3 |
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author | Deng, Lihua Li, Tiange Ling, Yunfei Tang, Menglin |
author_facet | Deng, Lihua Li, Tiange Ling, Yunfei Tang, Menglin |
author_sort | Deng, Lihua |
collection | PubMed |
description | BACKGROUND: Anomalous aortic origin of a coronary artery (AAOCA) is a rare congenital heart disease, characterized by the coronary artery inappropriately originates from the aorta. It is usually classified according to the sinus where the coronary artery arises from, while anomalous origin of the right coronary being the most common type. CASE PRESENTATION: In this case report, we described a rare case of Tetralogy of Fallot (TOF) in a 1-year-old boy, who also had the anomalous right coronary artery that originated from the left coronary sinus without an intramural segment. Besides TOF repair, lateral pulmonary translocation was undertaken in order to avoid risks of myocardial ischemia. CONCLUSION: We successfully completed a one-stage operation consisting of TOF repair and pulmonary artery translocation in a 1-year-old boy. We advocated early operation of pulmonic translocation for AAOCA patients without an intramural segment instead of unroofing procedure. |
format | Online Article Text |
id | pubmed-8557548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85575482021-11-01 Tetralogy of fallot in addition to anomalous aortic origin of a coronary artery in a 1-year-old boy: a case report Deng, Lihua Li, Tiange Ling, Yunfei Tang, Menglin BMC Surg Case Report BACKGROUND: Anomalous aortic origin of a coronary artery (AAOCA) is a rare congenital heart disease, characterized by the coronary artery inappropriately originates from the aorta. It is usually classified according to the sinus where the coronary artery arises from, while anomalous origin of the right coronary being the most common type. CASE PRESENTATION: In this case report, we described a rare case of Tetralogy of Fallot (TOF) in a 1-year-old boy, who also had the anomalous right coronary artery that originated from the left coronary sinus without an intramural segment. Besides TOF repair, lateral pulmonary translocation was undertaken in order to avoid risks of myocardial ischemia. CONCLUSION: We successfully completed a one-stage operation consisting of TOF repair and pulmonary artery translocation in a 1-year-old boy. We advocated early operation of pulmonic translocation for AAOCA patients without an intramural segment instead of unroofing procedure. BioMed Central 2021-10-30 /pmc/articles/PMC8557548/ /pubmed/34717598 http://dx.doi.org/10.1186/s12893-021-01380-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Deng, Lihua Li, Tiange Ling, Yunfei Tang, Menglin Tetralogy of fallot in addition to anomalous aortic origin of a coronary artery in a 1-year-old boy: a case report |
title | Tetralogy of fallot in addition to anomalous aortic origin of a coronary artery in a 1-year-old boy: a case report |
title_full | Tetralogy of fallot in addition to anomalous aortic origin of a coronary artery in a 1-year-old boy: a case report |
title_fullStr | Tetralogy of fallot in addition to anomalous aortic origin of a coronary artery in a 1-year-old boy: a case report |
title_full_unstemmed | Tetralogy of fallot in addition to anomalous aortic origin of a coronary artery in a 1-year-old boy: a case report |
title_short | Tetralogy of fallot in addition to anomalous aortic origin of a coronary artery in a 1-year-old boy: a case report |
title_sort | tetralogy of fallot in addition to anomalous aortic origin of a coronary artery in a 1-year-old boy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557548/ https://www.ncbi.nlm.nih.gov/pubmed/34717598 http://dx.doi.org/10.1186/s12893-021-01380-3 |
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