Abstract

Arrhythmogenic right ventricular dysplasia (ARVD) is an abnormality in the right side of the heart that may lead to sudden death. The study aims to compare cardiac MRI (magnetic resonance imaging findings) with echocardiography in patients with ARVD. For the cross-sectional study, patients with ARVD that were diagnosed using Task Force criteria were included, and their cardiac MRI findings were evaluated. Additionally, the right ventricle was divided into three levels—basal, middle, and apical—and each of them was also subdivided into three secondary segments. Gadolinium enhancement was evaluated in each segment. Overall, 39 patients were studied. Thirty-one patients (81%) were men. The average age of female and male patients was 37.8 ± 4.6 and 32.48 ± 5.8, respectively. The average ejection fraction found was 43 ± 9.4 and 42.8 ± 8.5% by MRI and echocardiography, respectively. Additionally, 46 and 35.8% of the patients had hypokinesia in the right ventricle, found based on MRI and echocardiography, respectively. The right ventricular aneurysm was found in 20.5 and 5.1% of patients based on MRI and echocardiography, respectively. The cardiac MRI managed to diagnose some cases which echocardiography was not able to detect. Thus, MRI plays an important role in presenting diagnostic data for the management of patients with ARVD and also making the diagnosis in suspicious patients definitive.

Highlights

  • Arrhythmogenic right ventricular dysplasia (ARVD) is a type of cardiomyopathy that primarily affects the heart muscle function and is frequently familial and observed sporadically [1].Arrhythmogenic right ventricular dysplasia accounts for 5% of sudden death in adults

  • Arrhythmogenic right ventricular dysplasia is a disorder with diagnostic features and aspects

  • Arrhythmogenic right ventricular dysplasia is a disorder with diagnostic features and aspects which are not completely known yet

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Summary

Introduction

Arrhythmogenic right ventricular dysplasia (ARVD) is a type of cardiomyopathy that primarily affects the heart muscle function and is frequently familial and observed sporadically [1].Arrhythmogenic right ventricular dysplasia accounts for 5% of sudden death in adults. Arrhythmogenic right ventricular dysplasia (ARVD) is a type of cardiomyopathy that primarily affects the heart muscle function and is frequently familial and observed sporadically [1]. In ARVD, the cells of the heart muscle, mainly right ventricle, are replaced by fat and fibrous tissue. The first one is Fibrolipomatosis Type 1 in which more fat tissue along with a small amount of fibrous tissue enclosed by healthy myocytes is observed. In this type, wall thickness increases and right ventricular pseudohypertrophy occurs. In Fibrolipomatosis Type 2, myocytes are extensively replaced by fat and fibrous tissue, which leads to saccular aneurysm and ventricular septal aneurysm [4]

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