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Unilateral pulmonary artery agenesis: An unusual cause of hemoptysis

INTRODUCTION: Unilateral pulmonary artery agenesis (UPAA) is a rare congenital malformation of the pulmonary artery due to agenesis of the sixth aortic arch during embryogenesis. Diagnosis can be challenging due to variable clinical presentations. CASE: A 29-year-old female at third trimester of twi...

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Autores principales: Wong, Yen Shen, Abidin, Zakhirati Zainol, Musa, Aisya Natasya, Kadir, Roqiah Fatmawati Abdul, Johari, Bushra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025273/
https://www.ncbi.nlm.nih.gov/pubmed/36950023
http://dx.doi.org/10.1016/j.rmcr.2023.101834
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author Wong, Yen Shen
Abidin, Zakhirati Zainol
Musa, Aisya Natasya
Kadir, Roqiah Fatmawati Abdul
Johari, Bushra
author_facet Wong, Yen Shen
Abidin, Zakhirati Zainol
Musa, Aisya Natasya
Kadir, Roqiah Fatmawati Abdul
Johari, Bushra
author_sort Wong, Yen Shen
collection PubMed
description INTRODUCTION: Unilateral pulmonary artery agenesis (UPAA) is a rare congenital malformation of the pulmonary artery due to agenesis of the sixth aortic arch during embryogenesis. Diagnosis can be challenging due to variable clinical presentations. CASE: A 29-year-old female at third trimester of twin pregnancy presented with massive hemoptysis. Computed tomography angiogram (CTA) showed unilateral absence of the right pulmonary artery with multiple dilated tortuous bronchial arteries supplying the right lung. Selective embolization of the bronchial artery was performed post-partum. CONCLUSION: Clinicians should have a high clinical suspicion of collateral artery bleeding in patients who present with unexplained hemoptysis and typical UPAA radiographic findings.
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spelling pubmed-100252732023-03-21 Unilateral pulmonary artery agenesis: An unusual cause of hemoptysis Wong, Yen Shen Abidin, Zakhirati Zainol Musa, Aisya Natasya Kadir, Roqiah Fatmawati Abdul Johari, Bushra Respir Med Case Rep Case Report INTRODUCTION: Unilateral pulmonary artery agenesis (UPAA) is a rare congenital malformation of the pulmonary artery due to agenesis of the sixth aortic arch during embryogenesis. Diagnosis can be challenging due to variable clinical presentations. CASE: A 29-year-old female at third trimester of twin pregnancy presented with massive hemoptysis. Computed tomography angiogram (CTA) showed unilateral absence of the right pulmonary artery with multiple dilated tortuous bronchial arteries supplying the right lung. Selective embolization of the bronchial artery was performed post-partum. CONCLUSION: Clinicians should have a high clinical suspicion of collateral artery bleeding in patients who present with unexplained hemoptysis and typical UPAA radiographic findings. Elsevier 2023-03-10 /pmc/articles/PMC10025273/ /pubmed/36950023 http://dx.doi.org/10.1016/j.rmcr.2023.101834 Text en © 2023 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Wong, Yen Shen
Abidin, Zakhirati Zainol
Musa, Aisya Natasya
Kadir, Roqiah Fatmawati Abdul
Johari, Bushra
Unilateral pulmonary artery agenesis: An unusual cause of hemoptysis
title Unilateral pulmonary artery agenesis: An unusual cause of hemoptysis
title_full Unilateral pulmonary artery agenesis: An unusual cause of hemoptysis
title_fullStr Unilateral pulmonary artery agenesis: An unusual cause of hemoptysis
title_full_unstemmed Unilateral pulmonary artery agenesis: An unusual cause of hemoptysis
title_short Unilateral pulmonary artery agenesis: An unusual cause of hemoptysis
title_sort unilateral pulmonary artery agenesis: an unusual cause of hemoptysis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025273/
https://www.ncbi.nlm.nih.gov/pubmed/36950023
http://dx.doi.org/10.1016/j.rmcr.2023.101834
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