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Pulmonary Arteriovenous Malformation in a Patient with Suspected Hereditary Hemorrhagic Telangiectasia: A Case Report

Hemoptysis is a common presenting symptom of hereditary hemorrhagic telangiectasia (HHT), an often overlooked diagnosis in the emergency setting. Patient history often includes telangiectasias, epistaxis, visceral lesions, and a family history of similar findings. Here, we review a case of HHT in a...

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Autores principales: Zuabi, Nadia, Thompson, Sean Ryan, Lucas, Alexa, Wray, Alisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Department of Emergency Medicine, University of California, Irvine School of Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332757/
https://www.ncbi.nlm.nih.gov/pubmed/37465542
http://dx.doi.org/10.21980/J8M353
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author Zuabi, Nadia
Thompson, Sean Ryan
Lucas, Alexa
Wray, Alisa
author_facet Zuabi, Nadia
Thompson, Sean Ryan
Lucas, Alexa
Wray, Alisa
author_sort Zuabi, Nadia
collection PubMed
description Hemoptysis is a common presenting symptom of hereditary hemorrhagic telangiectasia (HHT), an often overlooked diagnosis in the emergency setting. Patient history often includes telangiectasias, epistaxis, visceral lesions, and a family history of similar findings. Here, we review a case of HHT in a young woman, presenting initially with hemoptysis. Imaging was significant for large left upper lobe arteriovenous malformation (AVM), requiring patient admission and interventional radiology embolization of the AVM. The purpose of this report is to highlight a diagnosis that is important not to miss in the emergency department. TOPICS: Pulmonary arteriovenous malformation, hereditary hemorrhagic telangiectasia, Osler-Weber-Rendu syndrome.
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spelling pubmed-103327572023-07-18 Pulmonary Arteriovenous Malformation in a Patient with Suspected Hereditary Hemorrhagic Telangiectasia: A Case Report Zuabi, Nadia Thompson, Sean Ryan Lucas, Alexa Wray, Alisa J Educ Teach Emerg Med Visual EM Hemoptysis is a common presenting symptom of hereditary hemorrhagic telangiectasia (HHT), an often overlooked diagnosis in the emergency setting. Patient history often includes telangiectasias, epistaxis, visceral lesions, and a family history of similar findings. Here, we review a case of HHT in a young woman, presenting initially with hemoptysis. Imaging was significant for large left upper lobe arteriovenous malformation (AVM), requiring patient admission and interventional radiology embolization of the AVM. The purpose of this report is to highlight a diagnosis that is important not to miss in the emergency department. TOPICS: Pulmonary arteriovenous malformation, hereditary hemorrhagic telangiectasia, Osler-Weber-Rendu syndrome. Department of Emergency Medicine, University of California, Irvine School of Medicine 2021-01-15 /pmc/articles/PMC10332757/ /pubmed/37465542 http://dx.doi.org/10.21980/J8M353 Text en © 2021 Zuabi, et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) License. See: http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Visual EM
Zuabi, Nadia
Thompson, Sean Ryan
Lucas, Alexa
Wray, Alisa
Pulmonary Arteriovenous Malformation in a Patient with Suspected Hereditary Hemorrhagic Telangiectasia: A Case Report
title Pulmonary Arteriovenous Malformation in a Patient with Suspected Hereditary Hemorrhagic Telangiectasia: A Case Report
title_full Pulmonary Arteriovenous Malformation in a Patient with Suspected Hereditary Hemorrhagic Telangiectasia: A Case Report
title_fullStr Pulmonary Arteriovenous Malformation in a Patient with Suspected Hereditary Hemorrhagic Telangiectasia: A Case Report
title_full_unstemmed Pulmonary Arteriovenous Malformation in a Patient with Suspected Hereditary Hemorrhagic Telangiectasia: A Case Report
title_short Pulmonary Arteriovenous Malformation in a Patient with Suspected Hereditary Hemorrhagic Telangiectasia: A Case Report
title_sort pulmonary arteriovenous malformation in a patient with suspected hereditary hemorrhagic telangiectasia: a case report
topic Visual EM
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332757/
https://www.ncbi.nlm.nih.gov/pubmed/37465542
http://dx.doi.org/10.21980/J8M353
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