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Pulmonary Arteriovenous Malformation in a Rare Case of Hereditary Hemorrhagic Telangiectasia

Hereditary hemorrhagic telangiectasia is a rare condition presenting with anemia requiring transfusion and nosebleeds often refractory to supportive therapy. We discuss a case of a male in his 60s with a history of epistaxis, anemia requiring transfusions, and acute on chronic worsening shortness of...

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Autores principales: Azad, Farhan, Miranda, Clive J, Sparacino, Gina M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826734/
https://www.ncbi.nlm.nih.gov/pubmed/36627987
http://dx.doi.org/10.7759/cureus.32365
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author Azad, Farhan
Miranda, Clive J
Sparacino, Gina M
author_facet Azad, Farhan
Miranda, Clive J
Sparacino, Gina M
author_sort Azad, Farhan
collection PubMed
description Hereditary hemorrhagic telangiectasia is a rare condition presenting with anemia requiring transfusion and nosebleeds often refractory to supportive therapy. We discuss a case of a male in his 60s with a history of epistaxis, anemia requiring transfusions, and acute on chronic worsening shortness of breath presenting for evaluation. He was diagnosed with hereditary hemorrhagic telangiectasia. In addition, he was found to have pulmonary arteriovenous malformations and nonbleeding gastric telangiectasias. The patient underwent coil embolization of pulmonary arteriovenous malformations with a resolution of his shortness of breath and his anemia improved with iron supplementation.
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spelling pubmed-98267342023-01-09 Pulmonary Arteriovenous Malformation in a Rare Case of Hereditary Hemorrhagic Telangiectasia Azad, Farhan Miranda, Clive J Sparacino, Gina M Cureus Internal Medicine Hereditary hemorrhagic telangiectasia is a rare condition presenting with anemia requiring transfusion and nosebleeds often refractory to supportive therapy. We discuss a case of a male in his 60s with a history of epistaxis, anemia requiring transfusions, and acute on chronic worsening shortness of breath presenting for evaluation. He was diagnosed with hereditary hemorrhagic telangiectasia. In addition, he was found to have pulmonary arteriovenous malformations and nonbleeding gastric telangiectasias. The patient underwent coil embolization of pulmonary arteriovenous malformations with a resolution of his shortness of breath and his anemia improved with iron supplementation. Cureus 2022-12-09 /pmc/articles/PMC9826734/ /pubmed/36627987 http://dx.doi.org/10.7759/cureus.32365 Text en Copyright © 2022, Azad et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Azad, Farhan
Miranda, Clive J
Sparacino, Gina M
Pulmonary Arteriovenous Malformation in a Rare Case of Hereditary Hemorrhagic Telangiectasia
title Pulmonary Arteriovenous Malformation in a Rare Case of Hereditary Hemorrhagic Telangiectasia
title_full Pulmonary Arteriovenous Malformation in a Rare Case of Hereditary Hemorrhagic Telangiectasia
title_fullStr Pulmonary Arteriovenous Malformation in a Rare Case of Hereditary Hemorrhagic Telangiectasia
title_full_unstemmed Pulmonary Arteriovenous Malformation in a Rare Case of Hereditary Hemorrhagic Telangiectasia
title_short Pulmonary Arteriovenous Malformation in a Rare Case of Hereditary Hemorrhagic Telangiectasia
title_sort pulmonary arteriovenous malformation in a rare case of hereditary hemorrhagic telangiectasia
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826734/
https://www.ncbi.nlm.nih.gov/pubmed/36627987
http://dx.doi.org/10.7759/cureus.32365
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