Hereditary Apolipoprotein A-I–Associated Cardiac Amyloidosis: Importance of Endomyocardial Biopsy When Suspicion Remains High

Cardiac amyloidosis has recently garnered substantial attention. Although the advent of noninvasive diagnostic algorithms revolutionized diagnosis, endomyocardial biopsy may still be considered in select cases to determine the amyloidosis subtype definitively. We report a case of a patients with a k...

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Detalles Bibliográficos
Autores principales: Saleem, Maryam, Balla, Sudarshan, Amin, Md. Shahrier, Farid, Saira, Caccamo, Marco, Sokos, George, Bianco, Christopher M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311363/
https://www.ncbi.nlm.nih.gov/pubmed/34317679
http://dx.doi.org/10.1016/j.jaccas.2021.02.016
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author Saleem, Maryam
Balla, Sudarshan
Amin, Md. Shahrier
Farid, Saira
Caccamo, Marco
Sokos, George
Bianco, Christopher M.
author_facet Saleem, Maryam
Balla, Sudarshan
Amin, Md. Shahrier
Farid, Saira
Caccamo, Marco
Sokos, George
Bianco, Christopher M.
author_sort Saleem, Maryam
collection PubMed
description Cardiac amyloidosis has recently garnered substantial attention. Although the advent of noninvasive diagnostic algorithms revolutionized diagnosis, endomyocardial biopsy may still be considered in select cases to determine the amyloidosis subtype definitively. We report a case of a patients with a known mutation causing hereditary apolipoprotein A-I–associated cardiac amyloidosis. (Level of Difficulty: Advanced.)
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spelling pubmed-83113632021-07-26 Hereditary Apolipoprotein A-I–Associated Cardiac Amyloidosis: Importance of Endomyocardial Biopsy When Suspicion Remains High Saleem, Maryam Balla, Sudarshan Amin, Md. Shahrier Farid, Saira Caccamo, Marco Sokos, George Bianco, Christopher M. JACC Case Rep Case Report Cardiac amyloidosis has recently garnered substantial attention. Although the advent of noninvasive diagnostic algorithms revolutionized diagnosis, endomyocardial biopsy may still be considered in select cases to determine the amyloidosis subtype definitively. We report a case of a patients with a known mutation causing hereditary apolipoprotein A-I–associated cardiac amyloidosis. (Level of Difficulty: Advanced.) Elsevier 2021-07-07 /pmc/articles/PMC8311363/ /pubmed/34317679 http://dx.doi.org/10.1016/j.jaccas.2021.02.016 Text en © 2021 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 Case Report
Saleem, Maryam
Balla, Sudarshan
Amin, Md. Shahrier
Farid, Saira
Caccamo, Marco
Sokos, George
Bianco, Christopher M.
Hereditary Apolipoprotein A-I–Associated Cardiac Amyloidosis: Importance of Endomyocardial Biopsy When Suspicion Remains High
title Hereditary Apolipoprotein A-I–Associated Cardiac Amyloidosis: Importance of Endomyocardial Biopsy When Suspicion Remains High
title_full Hereditary Apolipoprotein A-I–Associated Cardiac Amyloidosis: Importance of Endomyocardial Biopsy When Suspicion Remains High
title_fullStr Hereditary Apolipoprotein A-I–Associated Cardiac Amyloidosis: Importance of Endomyocardial Biopsy When Suspicion Remains High
title_full_unstemmed Hereditary Apolipoprotein A-I–Associated Cardiac Amyloidosis: Importance of Endomyocardial Biopsy When Suspicion Remains High
title_short Hereditary Apolipoprotein A-I–Associated Cardiac Amyloidosis: Importance of Endomyocardial Biopsy When Suspicion Remains High
title_sort hereditary apolipoprotein a-i–associated cardiac amyloidosis: importance of endomyocardial biopsy when suspicion remains high
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311363/
https://www.ncbi.nlm.nih.gov/pubmed/34317679
http://dx.doi.org/10.1016/j.jaccas.2021.02.016
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