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Updated: Sep 5, 2025

Cardiac Magnetic Resonance for the Evaluation of Suspected Cardiac Thrombus: Conventional and Emerging Techniques
Published on: June 11, 2019
Cardiac magnetic resonance imaging of arrhythmogenic cardiomyopathy: evolving diagnostic perspectives
Alberto Cipriani1,2, Giulia Mattesi2, Riccardo Bariani1
1Department of Cardio-Thoraco-Vascular Sciences and Public Health, University of Padua, Via Giustiniani, 2, 35128, Padua, Italy.
Insights
Arrhythmogenic cardiomyopathy (ACM) is a genetic heart disease. Cardiac magnetic resonance (CMR) is now the preferred imaging technique for diagnosing all ACM phenotypes, including left ventricular variants, using updated criteria.
Area of Science:
- Cardiology
- Medical Imaging
- Genetics
Background:
- Arrhythmogenic cardiomyopathy (ACM) is a genetic heart muscle disease featuring fibro-fatty replacement.
- It is linked to ventricular arrhythmias and sudden cardiac death.
- ACM presents with right ventricular, left dominant, or biventricular phenotypes.
Purpose of the Study:
- To review the role of cardiac magnetic resonance (CMR) in diagnosing the full spectrum of ACM phenotypes.
- To highlight updated diagnostic criteria (2020 Padua Criteria) and CMR's importance.
- To detail ACM-specific CMR protocols and discuss imaging technique strengths and weaknesses.
Main Methods:
- Review of current literature on cardiac magnetic resonance in arrhythmogenic cardiomyopathy.
- Focus on the 2020 Padua Criteria for ACM diagnosis.
- Inclusion of ACM-specific CMR protocols and comparative analysis of imaging modalities.
Main Results:
- Cardiac magnetic resonance (CMR) is the imaging technique of choice for diagnosing all ACM phenotypes, including left ventricular variants.
- CMR offers detailed morpho-functional and tissue characterization of both right and left ventricles.
- The review outlines the supplemental value of CMR in characterizing disease variants.
Conclusions:
- Cardiac magnetic resonance (CMR) plays a pivotal role in the updated diagnosis of arrhythmogenic cardiomyopathy (ACM).
- CMR enables comprehensive evaluation across all ACM phenotypes, aiding in diagnosis and characterization.
- Understanding CMR findings is crucial for assessing the prognostic significance in ACM patients.
Abstract:
Arrhythmogenic cardiomyopathy (ACM) is a genetically determined heart muscle disease characterized by fibro-fatty myocardial replacement, clinically associated with malignant ventricular arrhythmias and sudden cardiac death. Originally described a disease with a prevalent right ventricular (RV) involvement, subsequently two other phenotypes have been recognized, such as the left dominant and the biventricular phenotypes, for which a recent International Expert consensus document provided upgrade diagnostic criteria (the 2020 "Padua Criteria"). In this novel workup for the diagnosis of the entire spectrum of phenotypic variants of ACM, including left ventricular (LV) variants, cardiac magnetic resonance (CMR) has emerged as the cardiac imaging technique of choice, due to its capability of detailed morpho-functional and tissue characterization evaluation of both RV and LV. In this review, the key role of CMR in the diagnosis of ACM is outlined, including the supplemental value for the characterization of the disease variants. An ACM-specific CMR study protocol, as well as strengths and weaknesses of each imaging technique, is also provided. KEY POINTS: • Arrhythmogenic cardiomyopathy includes three different phenotypes: dominant right, biventricular, and dominant left. • In 2020, diagnostic criteria have been updated and cardiac magnetic resonance has emerged as the cardiac imaging technique of choice. • This aim of this review is to provide an update of the current state of art regarding the use of CMR in ACM, with a particular focus on novel diagnostic criteria, CMR protocols, and prognostic significance of CMR findings in ACM.
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