Literature DB >> 22030343

[Arrhythmogenic cardiomyopathy. Patterns of ventricular involvement using cardiac magnetic resonance].

Begoña Igual1, Esther Zorio, Alicia Maceira, Jordi Estornell, María P Lopez-Lereu, Jose V Monmeneu, Anastasio Quesada, Josep Navarro, Fernando Mas, Antonio Salvador.   

Abstract

INTRODUCTION AND
OBJECTIVES: Biventricular arrhythmogenic cardiomyopathy and left dominant arrhythmogenic cardiomyopathy forms had recently been included in the spectrum of arrhythmogenic cardiomyopathy. The aim of the study was to describe, using cardiovascular magnetic resonance, the patterns of ventricular involvement as well as late gadolinium enhancement in these conditions.
METHODS: Medical databases and records from the cardiology units of 3 hospitals were reviewed to obtain data from patients with arrhythmogenic cardiomyopathy.
RESULTS: Twenty-six consecutive patients were included (40 [16] years, 16 males). Right ventricle involvement was present in 19 patients (73%). Among them, 13 patients (50%) had volumes over the upper limit of normality, 11 (42%) patients had late gadolinium enhancement in right ventricle and 6 patients (23%) had just mild involvement with wall motion abnormalities or microaneurysms. Left ventricle involvement was present in 24 patients (92%), all of them with late gadolinium enhancement. In 15 patients (57%) left ventricular systolic dysfunction was observed, and dilatation in 3 patients (11%). Late gadolinium enhancement was more frequent in the inferior, lateral, and inferolateral walls (65%, 57%, and 61% of patients, respectively) while septum was seldom affected (26% of cases). The pattern of late gadolinium enhancement was mainly subepicardial (46% of patients) or transmural (19%), and was intramyocardial in only 12% of the cases.
CONCLUSIONS: In this sample, left ventricle involvement is very common. The most frequent finding was left ventricular late gadolinium enhancement, while the least frequent was dilatation. The pattern of late gadolinium enhancement was more frequently subepicardial and located in the inferior and inferolateral walls.
Copyright © 2010 Sociedad Española de Cardiología. Published by Elsevier Espana. All rights reserved.

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Year:  2011        PMID: 22030343     DOI: 10.1016/j.recesp.2011.07.014

Source DB:  PubMed          Journal:  Rev Esp Cardiol        ISSN: 0300-8932            Impact factor:   4.753


  5 in total

1.  Atypical clinical presentation of arrhythmogenic biventricular cardiomyopathy.

Authors:  Inês Rangel; Mariana Vasconcelos; Manuel Campelo; Cecília Frutuoso; António José Madureira; Maria Júlia Maciel
Journal:  Arq Bras Cardiol       Date:  2014-01       Impact factor: 2.000

Review 2.  Arrhythmogenic right ventricular cardiomyopathy (ARVC): cardiovascular magnetic resonance update.

Authors:  Anneline S J M te Riele; Harikrishna Tandri; David A Bluemke
Journal:  J Cardiovasc Magn Reson       Date:  2014-07-20       Impact factor: 5.364

3.  Arrhythmogenic cardiomyopathy with left ventricular involvement versus ischemic heart disease: lessons learned from the family study and the reviewed autopsy of a young male.

Authors:  Pilar Molina; Jorge Sanz-Sánchez; Manuel Fenollosa; Marina Martínez-Matilla; Juan Giner; Esther Zorio
Journal:  Forensic Sci Res       Date:  2019-08-19

Review 4.  How to interpret right ventricular remodeling in athletes.

Authors:  María Sanz-de la Garza; Amelia Carro; Stefano Caselli
Journal:  Clin Cardiol       Date:  2020-03-04       Impact factor: 2.882

Review 5.  Arrhythmogenic Left Ventricular Cardiomyopathy: Genotype-Phenotype Correlations and New Diagnostic Criteria.

Authors:  Giulia Mattesi; Alberto Cipriani; Barbara Bauce; Ilaria Rigato; Alessandro Zorzi; Domenico Corrado
Journal:  J Clin Med       Date:  2021-05-20       Impact factor: 4.241

  5 in total

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