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Unilateral pulmonary vein atresia presenting with recurrent haemoptysis in a child: a case report
BACKGROUND: Haemoptysis is an uncommon presenting symptom in children and is usually caused by acute lower respiratory tract infection or foreign body aspiration. We report a rare case of right unilateral pulmonary vein atresia (PVA) as the underlying aetiology of recurrent haemoptysis in a child. C...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513278/ https://www.ncbi.nlm.nih.gov/pubmed/32972390 http://dx.doi.org/10.1186/s12887-020-02348-7 |
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author | Wong, Martin Ngie Liong Tang, Ing Ping Chor, Yek Kee Lau, Kiew Siong John, Anne Rachel Hii, King Ching Lee, Olive Pei Yi Lim, Wooi Kok Tan, Hannah Pei Koon |
author_facet | Wong, Martin Ngie Liong Tang, Ing Ping Chor, Yek Kee Lau, Kiew Siong John, Anne Rachel Hii, King Ching Lee, Olive Pei Yi Lim, Wooi Kok Tan, Hannah Pei Koon |
author_sort | Wong, Martin Ngie Liong |
collection | PubMed |
description | BACKGROUND: Haemoptysis is an uncommon presenting symptom in children and is usually caused by acute lower respiratory tract infection or foreign body aspiration. We report a rare case of right unilateral pulmonary vein atresia (PVA) as the underlying aetiology of recurrent haemoptysis in a child. CASE PRESENTATION: A 4 years old girl presented with history of recurrent haemoptysis. Bronchoscopic evaluation excluded a foreign body aspiration but revealed right bronchial mucosal hyperaemia and varices. Diagnosis of right unilateral PVA was suspected on transthoracic echocardiography which demonstrated hypoplastic right pulmonary artery and non-visualization of right pulmonary veins. Final diagnosis was confirmed on cardiac CT angiography. A conservative treatment approach was opted with consideration for pneumonectomy in future when she is older. CONCLUSION: Rarer causes should be considered when investigating for recurrent haemoptysis in children. Bronchoscopy and cardiac imaging are useful tools to establish the diagnosis of unilateral PVA in our case. |
format | Online Article Text |
id | pubmed-7513278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75132782020-09-25 Unilateral pulmonary vein atresia presenting with recurrent haemoptysis in a child: a case report Wong, Martin Ngie Liong Tang, Ing Ping Chor, Yek Kee Lau, Kiew Siong John, Anne Rachel Hii, King Ching Lee, Olive Pei Yi Lim, Wooi Kok Tan, Hannah Pei Koon BMC Pediatr Case Report BACKGROUND: Haemoptysis is an uncommon presenting symptom in children and is usually caused by acute lower respiratory tract infection or foreign body aspiration. We report a rare case of right unilateral pulmonary vein atresia (PVA) as the underlying aetiology of recurrent haemoptysis in a child. CASE PRESENTATION: A 4 years old girl presented with history of recurrent haemoptysis. Bronchoscopic evaluation excluded a foreign body aspiration but revealed right bronchial mucosal hyperaemia and varices. Diagnosis of right unilateral PVA was suspected on transthoracic echocardiography which demonstrated hypoplastic right pulmonary artery and non-visualization of right pulmonary veins. Final diagnosis was confirmed on cardiac CT angiography. A conservative treatment approach was opted with consideration for pneumonectomy in future when she is older. CONCLUSION: Rarer causes should be considered when investigating for recurrent haemoptysis in children. Bronchoscopy and cardiac imaging are useful tools to establish the diagnosis of unilateral PVA in our case. BioMed Central 2020-09-24 /pmc/articles/PMC7513278/ /pubmed/32972390 http://dx.doi.org/10.1186/s12887-020-02348-7 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Wong, Martin Ngie Liong Tang, Ing Ping Chor, Yek Kee Lau, Kiew Siong John, Anne Rachel Hii, King Ching Lee, Olive Pei Yi Lim, Wooi Kok Tan, Hannah Pei Koon Unilateral pulmonary vein atresia presenting with recurrent haemoptysis in a child: a case report |
title | Unilateral pulmonary vein atresia presenting with recurrent haemoptysis in a child: a case report |
title_full | Unilateral pulmonary vein atresia presenting with recurrent haemoptysis in a child: a case report |
title_fullStr | Unilateral pulmonary vein atresia presenting with recurrent haemoptysis in a child: a case report |
title_full_unstemmed | Unilateral pulmonary vein atresia presenting with recurrent haemoptysis in a child: a case report |
title_short | Unilateral pulmonary vein atresia presenting with recurrent haemoptysis in a child: a case report |
title_sort | unilateral pulmonary vein atresia presenting with recurrent haemoptysis in a child: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513278/ https://www.ncbi.nlm.nih.gov/pubmed/32972390 http://dx.doi.org/10.1186/s12887-020-02348-7 |
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