Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia

This report describes a case of embolic myocardial infarction secondary to a pulmonary arteriovenous malformation. Pulmonary arteriovenous malformations are rare and mostly congenital and are inherited as an autosomal dominant disorder known as hereditary hemorrhagic telangiectasia. Myocardial infar...

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Autores principales: Sánchez-Fernández, Gabriel, García-López, Fernando, Martínez-Bendayán, Isaac, Bello-Peón, María José, Marzoa-Rivas, Raquel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Imaging Vignette
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298302/
https://www.ncbi.nlm.nih.gov/pubmed/34317232
http://dx.doi.org/10.1016/j.jaccas.2019.11.046
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author Sánchez-Fernández, Gabriel
García-López, Fernando
Martínez-Bendayán, Isaac
Bello-Peón, María José
Marzoa-Rivas, Raquel
author_facet Sánchez-Fernández, Gabriel
García-López, Fernando
Martínez-Bendayán, Isaac
Bello-Peón, María José
Marzoa-Rivas, Raquel
author_sort Sánchez-Fernández, Gabriel
collection PubMed
description This report describes a case of embolic myocardial infarction secondary to a pulmonary arteriovenous malformation. Pulmonary arteriovenous malformations are rare and mostly congenital and are inherited as an autosomal dominant disorder known as hereditary hemorrhagic telangiectasia. Myocardial infarction is an uncommon complication in patients with untreated pulmonary arteriovenous malformations. (Level of Difficulty: Advanced.)
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spelling pubmed-82983022021-07-26 Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia Sánchez-Fernández, Gabriel García-López, Fernando Martínez-Bendayán, Isaac Bello-Peón, María José Marzoa-Rivas, Raquel JACC Case Rep Imaging Vignette This report describes a case of embolic myocardial infarction secondary to a pulmonary arteriovenous malformation. Pulmonary arteriovenous malformations are rare and mostly congenital and are inherited as an autosomal dominant disorder known as hereditary hemorrhagic telangiectasia. Myocardial infarction is an uncommon complication in patients with untreated pulmonary arteriovenous malformations. (Level of Difficulty: Advanced.) Elsevier 2020-02-19 /pmc/articles/PMC8298302/ /pubmed/34317232 http://dx.doi.org/10.1016/j.jaccas.2019.11.046 Text en © 2020 The Authors 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 Imaging Vignette
Sánchez-Fernández, Gabriel
García-López, Fernando
Martínez-Bendayán, Isaac
Bello-Peón, María José
Marzoa-Rivas, Raquel
Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia
title Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia
title_full Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia
title_fullStr Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia
title_full_unstemmed Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia
title_short Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia
title_sort pulmonary arteriovenous malformation and embolic myocardial infarction in a patient with hereditary hemorrhagic telangiectasia
topic Imaging Vignette
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298302/
https://www.ncbi.nlm.nih.gov/pubmed/34317232
http://dx.doi.org/10.1016/j.jaccas.2019.11.046
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