A case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation

Pulmonary arteriovenous malformation (PAVM) is a rare vascular anomaly characterized by abnormal communication between the pulmonary artery and vein. It is a rare cause of hemoptysis. Computed tomographic angiography (CTA) has become the preferred and dependable diagnostic approach for identifying P...

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Autores principales: Thapa, Paras, Bhattarai, Madhur, Sharma Paudel, Basanta, Kunwar, Pratiksha, Chataut, Dinesh, Bhandari, Shailaj, Bhandari, Sagar, Paudel, Pratiksha, Sharma, Prakash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10480646/
https://www.ncbi.nlm.nih.gov/pubmed/37680652
http://dx.doi.org/10.1016/j.radcr.2023.08.057
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author Thapa, Paras
Bhattarai, Madhur
Sharma Paudel, Basanta
Kunwar, Pratiksha
Chataut, Dinesh
Bhandari, Shailaj
Bhandari, Sagar
Paudel, Pratiksha
Sharma, Prakash
author_facet Thapa, Paras
Bhattarai, Madhur
Sharma Paudel, Basanta
Kunwar, Pratiksha
Chataut, Dinesh
Bhandari, Shailaj
Bhandari, Sagar
Paudel, Pratiksha
Sharma, Prakash
author_sort Thapa, Paras
collection PubMed
description Pulmonary arteriovenous malformation (PAVM) is a rare vascular anomaly characterized by abnormal communication between the pulmonary artery and vein. It is a rare cause of hemoptysis. Computed tomographic angiography (CTA) has become the preferred and dependable diagnostic approach for identifying PAVM. PAVM embolization is the primary recommended treatment for this condition. We present a case of a 43-year-old male with a complex PAVM in the left lower lobe presenting with hemoptysis treated with an endovascular approach. Following the procedure, the patient's symptoms resolved.
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spelling pubmed-104806462023-09-07 A case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation Thapa, Paras Bhattarai, Madhur Sharma Paudel, Basanta Kunwar, Pratiksha Chataut, Dinesh Bhandari, Shailaj Bhandari, Sagar Paudel, Pratiksha Sharma, Prakash Radiol Case Rep Case Report Pulmonary arteriovenous malformation (PAVM) is a rare vascular anomaly characterized by abnormal communication between the pulmonary artery and vein. It is a rare cause of hemoptysis. Computed tomographic angiography (CTA) has become the preferred and dependable diagnostic approach for identifying PAVM. PAVM embolization is the primary recommended treatment for this condition. We present a case of a 43-year-old male with a complex PAVM in the left lower lobe presenting with hemoptysis treated with an endovascular approach. Following the procedure, the patient's symptoms resolved. Elsevier 2023-09-02 /pmc/articles/PMC10480646/ /pubmed/37680652 http://dx.doi.org/10.1016/j.radcr.2023.08.057 Text en © 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington. 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
Thapa, Paras
Bhattarai, Madhur
Sharma Paudel, Basanta
Kunwar, Pratiksha
Chataut, Dinesh
Bhandari, Shailaj
Bhandari, Sagar
Paudel, Pratiksha
Sharma, Prakash
A case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation
title A case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation
title_full A case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation
title_fullStr A case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation
title_full_unstemmed A case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation
title_short A case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation
title_sort case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10480646/
https://www.ncbi.nlm.nih.gov/pubmed/37680652
http://dx.doi.org/10.1016/j.radcr.2023.08.057
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