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Case report: Multiple biventricular aneurysms in arrhythmogenic cardiomyopathy
Arrhythmogenic cardiomyopathy (ACM) is a genetic disease characterized by fibro-fatty myocardial replacement and is clinically associated with malignant ventricular arrhythmias and sudden cardiac death. It presents a major diagnostic and therapeutic challenge due to its complex clinical presentation...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902953/ https://www.ncbi.nlm.nih.gov/pubmed/36762301 http://dx.doi.org/10.3389/fcvm.2022.1034703 |
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author | Lin, Jiadong Lu, Zhijuang Lin, Mingqin Wan, Ying Li, Jianfeng Huang, Xinsheng |
author_facet | Lin, Jiadong Lu, Zhijuang Lin, Mingqin Wan, Ying Li, Jianfeng Huang, Xinsheng |
author_sort | Lin, Jiadong |
collection | PubMed |
description | Arrhythmogenic cardiomyopathy (ACM) is a genetic disease characterized by fibro-fatty myocardial replacement and is clinically associated with malignant ventricular arrhythmias and sudden cardiac death. It presents a major diagnostic and therapeutic challenge due to its complex clinical presentation and multiparametric diagnostic scoring system that includes structural, histological, and electrocardiographic data. A 57-year-old man with a history of palpitation and premature ventricular contractions (PVC) experienced syncope and sustained ventricular tachycardia at a rate of 213 bpm, which was successfully rescued by synchronized cardioversion. Multiple ventricular aneurysms were found in the right ventricular free wall and the left ventricular apical regions, as well as mild biventricular systolic dysfunction, according to echocardiography and high-frequency ultrasound. The genetic analysis revealed the following desmoplakin genes, chr6-7585274-7585275, NM_004415, exon24, and c.7780delT (p.S2594Pfs(*)9), a heterozygous and likely pathogenic mutation, as the mutation sites in the patient and his 24-year-old daughter. During the 21-month follow-up, the patient did not experience syncope or pre-syncope symptoms while on β-blocker (bisoprolol) therapy. Among the multimodality imaging techniques of the ACM, late gadolinium enhancement on cardiac magnetic resonance (CMR) is accepted as a more objective indicator of myocardial fibrosis. Left ventricular systolic dysfunction, fibrosis on CMR, and frequent PVC are the primary and most sensitive clinical signs of desmoplakin cardiomyopathy. However, echocardiography continues to be the most commonly used imaging modality for assessing focal ventricular movement and structural abnormalities. The pathological characteristics of arrhythmogenic cardiomyopathy of the right ventricular anterior free wall and apical regions near the transducer can be better shown using high-frequency linear ultrasound with a higher resolution. |
format | Online Article Text |
id | pubmed-9902953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99029532023-02-08 Case report: Multiple biventricular aneurysms in arrhythmogenic cardiomyopathy Lin, Jiadong Lu, Zhijuang Lin, Mingqin Wan, Ying Li, Jianfeng Huang, Xinsheng Front Cardiovasc Med Cardiovascular Medicine Arrhythmogenic cardiomyopathy (ACM) is a genetic disease characterized by fibro-fatty myocardial replacement and is clinically associated with malignant ventricular arrhythmias and sudden cardiac death. It presents a major diagnostic and therapeutic challenge due to its complex clinical presentation and multiparametric diagnostic scoring system that includes structural, histological, and electrocardiographic data. A 57-year-old man with a history of palpitation and premature ventricular contractions (PVC) experienced syncope and sustained ventricular tachycardia at a rate of 213 bpm, which was successfully rescued by synchronized cardioversion. Multiple ventricular aneurysms were found in the right ventricular free wall and the left ventricular apical regions, as well as mild biventricular systolic dysfunction, according to echocardiography and high-frequency ultrasound. The genetic analysis revealed the following desmoplakin genes, chr6-7585274-7585275, NM_004415, exon24, and c.7780delT (p.S2594Pfs(*)9), a heterozygous and likely pathogenic mutation, as the mutation sites in the patient and his 24-year-old daughter. During the 21-month follow-up, the patient did not experience syncope or pre-syncope symptoms while on β-blocker (bisoprolol) therapy. Among the multimodality imaging techniques of the ACM, late gadolinium enhancement on cardiac magnetic resonance (CMR) is accepted as a more objective indicator of myocardial fibrosis. Left ventricular systolic dysfunction, fibrosis on CMR, and frequent PVC are the primary and most sensitive clinical signs of desmoplakin cardiomyopathy. However, echocardiography continues to be the most commonly used imaging modality for assessing focal ventricular movement and structural abnormalities. The pathological characteristics of arrhythmogenic cardiomyopathy of the right ventricular anterior free wall and apical regions near the transducer can be better shown using high-frequency linear ultrasound with a higher resolution. Frontiers Media S.A. 2023-01-24 /pmc/articles/PMC9902953/ /pubmed/36762301 http://dx.doi.org/10.3389/fcvm.2022.1034703 Text en Copyright © 2023 Lin, Lu, Lin, Wan, Li and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Lin, Jiadong Lu, Zhijuang Lin, Mingqin Wan, Ying Li, Jianfeng Huang, Xinsheng Case report: Multiple biventricular aneurysms in arrhythmogenic cardiomyopathy |
title | Case report: Multiple biventricular aneurysms in arrhythmogenic cardiomyopathy |
title_full | Case report: Multiple biventricular aneurysms in arrhythmogenic cardiomyopathy |
title_fullStr | Case report: Multiple biventricular aneurysms in arrhythmogenic cardiomyopathy |
title_full_unstemmed | Case report: Multiple biventricular aneurysms in arrhythmogenic cardiomyopathy |
title_short | Case report: Multiple biventricular aneurysms in arrhythmogenic cardiomyopathy |
title_sort | case report: multiple biventricular aneurysms in arrhythmogenic cardiomyopathy |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902953/ https://www.ncbi.nlm.nih.gov/pubmed/36762301 http://dx.doi.org/10.3389/fcvm.2022.1034703 |
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