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Arrhythmogenic left ventricular cardiomyopathy
Arrhythmogenic ventricular cardiomyopathy (AVC) is a heritable heart muscle disorder characterized by fibrofatty infiltration of the myocardium. Intramyocardial fat deposition is considered arrhythmogenic and predisposes patients to life-threatening arrhythmias and sudden cardiac death. The classic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The British Institute of Radiology.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068103/ https://www.ncbi.nlm.nih.gov/pubmed/32201615 http://dx.doi.org/10.1259/bjrcr.20190079 |
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author | Mirmomen, Seyedeh Mojdeh Bradley, Andrew Jay Arai, Andrew Ernest Sirajuddin, Arlene |
author_facet | Mirmomen, Seyedeh Mojdeh Bradley, Andrew Jay Arai, Andrew Ernest Sirajuddin, Arlene |
author_sort | Mirmomen, Seyedeh Mojdeh |
collection | PubMed |
description | Arrhythmogenic ventricular cardiomyopathy (AVC) is a heritable heart muscle disorder characterized by fibrofatty infiltration of the myocardium. Intramyocardial fat deposition is considered arrhythmogenic and predisposes patients to life-threatening arrhythmias and sudden cardiac death. The classic subtype of AVC is characterized by fibrofatty replacement of the right ventricular myocardium (i.e. arrhythmogenic right ventricular cardiomyopathy). In advanced cases of arrhythmogenic right ventricular cardiomyopathy, the left ventricle may be involved as well. Predominantly left ventricular involvement by AVC is exceedingly rare and lack of specific diagnostic criteria as well as its potential cardiotoxic effect make its diagnosis challenging and of high importance. |
format | Online Article Text |
id | pubmed-7068103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The British Institute of Radiology. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70681032020-03-20 Arrhythmogenic left ventricular cardiomyopathy Mirmomen, Seyedeh Mojdeh Bradley, Andrew Jay Arai, Andrew Ernest Sirajuddin, Arlene BJR Case Rep Case Report Arrhythmogenic ventricular cardiomyopathy (AVC) is a heritable heart muscle disorder characterized by fibrofatty infiltration of the myocardium. Intramyocardial fat deposition is considered arrhythmogenic and predisposes patients to life-threatening arrhythmias and sudden cardiac death. The classic subtype of AVC is characterized by fibrofatty replacement of the right ventricular myocardium (i.e. arrhythmogenic right ventricular cardiomyopathy). In advanced cases of arrhythmogenic right ventricular cardiomyopathy, the left ventricle may be involved as well. Predominantly left ventricular involvement by AVC is exceedingly rare and lack of specific diagnostic criteria as well as its potential cardiotoxic effect make its diagnosis challenging and of high importance. The British Institute of Radiology. 2020-02-12 /pmc/articles/PMC7068103/ /pubmed/32201615 http://dx.doi.org/10.1259/bjrcr.20190079 Text en © 2020 The Authors. Published by the British Institute of Radiology This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Case Report Mirmomen, Seyedeh Mojdeh Bradley, Andrew Jay Arai, Andrew Ernest Sirajuddin, Arlene Arrhythmogenic left ventricular cardiomyopathy |
title | Arrhythmogenic left ventricular cardiomyopathy |
title_full | Arrhythmogenic left ventricular cardiomyopathy |
title_fullStr | Arrhythmogenic left ventricular cardiomyopathy |
title_full_unstemmed | Arrhythmogenic left ventricular cardiomyopathy |
title_short | Arrhythmogenic left ventricular cardiomyopathy |
title_sort | arrhythmogenic left ventricular cardiomyopathy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068103/ https://www.ncbi.nlm.nih.gov/pubmed/32201615 http://dx.doi.org/10.1259/bjrcr.20190079 |
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