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Giant pulmonary artery aneurysm in a child: Rare complication of congenital heart disease
KEY CLINICAL MESSAGE: This case report aims to increase awareness that pulmonary artery aneurysms may occur as a complication of neglected patent ductus arteriosus and should be sought in children with ill‐treated congenital heart diseases. ABSTRACT: Pulmonary artery aneurysm is a rare anomaly with...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293579/ https://www.ncbi.nlm.nih.gov/pubmed/37384228 http://dx.doi.org/10.1002/ccr3.7622 |
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author | Hailu, Samuel Sisay Derbew, Hermon Miliard Zeray, Abrehet Hailemariam, Tesfahunegn Otero, Hansel J. |
author_facet | Hailu, Samuel Sisay Derbew, Hermon Miliard Zeray, Abrehet Hailemariam, Tesfahunegn Otero, Hansel J. |
author_sort | Hailu, Samuel Sisay |
collection | PubMed |
description | KEY CLINICAL MESSAGE: This case report aims to increase awareness that pulmonary artery aneurysms may occur as a complication of neglected patent ductus arteriosus and should be sought in children with ill‐treated congenital heart diseases. ABSTRACT: Pulmonary artery aneurysm is a rare anomaly with an autopsy prevalence of 1:14,000. These aneurysms can arise secondary to various etiologies, with congenital causes identified in 25% of cases and congenital heart diseases (CHD) responsible for more than half of these cases. A 12‐year‐old boy with CHD in the form of patent ductus arteriosus (PDA) and irregular clinical follow‐up presented with new onset fatigue of 3 months duration. A physical examination revealed anterior chest wall bulging and a continuous murmur. A chest radiograph showed a smooth left hilar region opacity that has a close relation with the left cardiac border. Transthoracic echocardiogram shows no progression from the previous one; there was a large PDA and pulmonary hypertension, but no further information was available. Computed tomography angiography revealed a giant aneurysm of the main pulmonary artery (PA), with a maximum diameter of 8.6 cm, and dilatation of its branches of 3.4 and 2.9 cm for the right and left PA, respectively. |
format | Online Article Text |
id | pubmed-10293579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102935792023-06-28 Giant pulmonary artery aneurysm in a child: Rare complication of congenital heart disease Hailu, Samuel Sisay Derbew, Hermon Miliard Zeray, Abrehet Hailemariam, Tesfahunegn Otero, Hansel J. Clin Case Rep Case Report KEY CLINICAL MESSAGE: This case report aims to increase awareness that pulmonary artery aneurysms may occur as a complication of neglected patent ductus arteriosus and should be sought in children with ill‐treated congenital heart diseases. ABSTRACT: Pulmonary artery aneurysm is a rare anomaly with an autopsy prevalence of 1:14,000. These aneurysms can arise secondary to various etiologies, with congenital causes identified in 25% of cases and congenital heart diseases (CHD) responsible for more than half of these cases. A 12‐year‐old boy with CHD in the form of patent ductus arteriosus (PDA) and irregular clinical follow‐up presented with new onset fatigue of 3 months duration. A physical examination revealed anterior chest wall bulging and a continuous murmur. A chest radiograph showed a smooth left hilar region opacity that has a close relation with the left cardiac border. Transthoracic echocardiogram shows no progression from the previous one; there was a large PDA and pulmonary hypertension, but no further information was available. Computed tomography angiography revealed a giant aneurysm of the main pulmonary artery (PA), with a maximum diameter of 8.6 cm, and dilatation of its branches of 3.4 and 2.9 cm for the right and left PA, respectively. John Wiley and Sons Inc. 2023-06-26 /pmc/articles/PMC10293579/ /pubmed/37384228 http://dx.doi.org/10.1002/ccr3.7622 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Report Hailu, Samuel Sisay Derbew, Hermon Miliard Zeray, Abrehet Hailemariam, Tesfahunegn Otero, Hansel J. Giant pulmonary artery aneurysm in a child: Rare complication of congenital heart disease |
title | Giant pulmonary artery aneurysm in a child: Rare complication of congenital heart disease |
title_full | Giant pulmonary artery aneurysm in a child: Rare complication of congenital heart disease |
title_fullStr | Giant pulmonary artery aneurysm in a child: Rare complication of congenital heart disease |
title_full_unstemmed | Giant pulmonary artery aneurysm in a child: Rare complication of congenital heart disease |
title_short | Giant pulmonary artery aneurysm in a child: Rare complication of congenital heart disease |
title_sort | giant pulmonary artery aneurysm in a child: rare complication of congenital heart disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293579/ https://www.ncbi.nlm.nih.gov/pubmed/37384228 http://dx.doi.org/10.1002/ccr3.7622 |
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