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Arrhythmogenic Right Ventricular Cardiomyopathy Accompanied by Chronic Myocarditis

Patients with arrhythmogenic right ventricular cardiomyopathy (ARVC) classically present with ventricular arrhythmias and less commonly heart failure. ARVC is an inherited cardiomyopathy and generally based on a variant of desmosomal genes. Recently, the association between myocardial inflammation a...

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Autores principales: Nakamura, Makiko, Imamura, Teruhiko, Fukui, Takuya, Kataoka, Naoya, Kinugawa, Koichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646355/
https://www.ncbi.nlm.nih.gov/pubmed/35342132
http://dx.doi.org/10.2169/internalmedicine.8911-21
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author Nakamura, Makiko
Imamura, Teruhiko
Fukui, Takuya
Kataoka, Naoya
Kinugawa, Koichiro
author_facet Nakamura, Makiko
Imamura, Teruhiko
Fukui, Takuya
Kataoka, Naoya
Kinugawa, Koichiro
author_sort Nakamura, Makiko
collection PubMed
description Patients with arrhythmogenic right ventricular cardiomyopathy (ARVC) classically present with ventricular arrhythmias and less commonly heart failure. ARVC is an inherited cardiomyopathy and generally based on a variant of desmosomal genes. Recently, the association between myocardial inflammation and ARVC has been a matter of great concern. We encountered a patient with ARVC who had a desmoglein-2 mutation with advanced right ventricular failure accompanying a preserved left ventricular function. Concomitant right ventricular myocarditis was detected four years after the diagnosis of ARVC. ARVC and myocarditis might have a deep pathophysiological association, at least in some cases.
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spelling pubmed-96463552022-11-18 Arrhythmogenic Right Ventricular Cardiomyopathy Accompanied by Chronic Myocarditis Nakamura, Makiko Imamura, Teruhiko Fukui, Takuya Kataoka, Naoya Kinugawa, Koichiro Intern Med Case Report Patients with arrhythmogenic right ventricular cardiomyopathy (ARVC) classically present with ventricular arrhythmias and less commonly heart failure. ARVC is an inherited cardiomyopathy and generally based on a variant of desmosomal genes. Recently, the association between myocardial inflammation and ARVC has been a matter of great concern. We encountered a patient with ARVC who had a desmoglein-2 mutation with advanced right ventricular failure accompanying a preserved left ventricular function. Concomitant right ventricular myocarditis was detected four years after the diagnosis of ARVC. ARVC and myocarditis might have a deep pathophysiological association, at least in some cases. The Japanese Society of Internal Medicine 2022-03-26 2022-10-15 /pmc/articles/PMC9646355/ /pubmed/35342132 http://dx.doi.org/10.2169/internalmedicine.8911-21 Text en Copyright © 2022 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Nakamura, Makiko
Imamura, Teruhiko
Fukui, Takuya
Kataoka, Naoya
Kinugawa, Koichiro
Arrhythmogenic Right Ventricular Cardiomyopathy Accompanied by Chronic Myocarditis
title Arrhythmogenic Right Ventricular Cardiomyopathy Accompanied by Chronic Myocarditis
title_full Arrhythmogenic Right Ventricular Cardiomyopathy Accompanied by Chronic Myocarditis
title_fullStr Arrhythmogenic Right Ventricular Cardiomyopathy Accompanied by Chronic Myocarditis
title_full_unstemmed Arrhythmogenic Right Ventricular Cardiomyopathy Accompanied by Chronic Myocarditis
title_short Arrhythmogenic Right Ventricular Cardiomyopathy Accompanied by Chronic Myocarditis
title_sort arrhythmogenic right ventricular cardiomyopathy accompanied by chronic myocarditis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646355/
https://www.ncbi.nlm.nih.gov/pubmed/35342132
http://dx.doi.org/10.2169/internalmedicine.8911-21
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