MRI Findings in Desmoplakin-related Arrhythmogenic Left Ventricular Cardiomyopathy in a Pediatric Patient: A Case Report.
George MorcosSudhir VashistRecai AktayPublished in: Radiology. Cardiothoracic imaging (2023)
Arrhythmogenic cardiomyopathy (ACM) is a heart muscle disorder that cannot be explained by ischemic, hypertensive, or valvular heart disease and often results in sudden cardiac death. Arrhythmogenic right ventricular cardiomyopathy (ARVC) is the best-characterized ACM and can be diagnosed using the revised task force criteria. In contrast, there are no accepted clinical diagnostic criteria for arrhythmogenic left ventricular cardiomyopathy (ALVC), another subtype of ACM. Cardiac MRI aids in ARVC diagnosis by delineating biventricular structural and functional abnormalities and can be instrumental in diagnosing ALVC. This report presents a pediatric case of desmoplakin cardiomyopathy, a distinct subtype of ALVC, with findings overlapping myocarditis and LV noncompaction. Keywords: Pediatrics, Heart, Cardiomyopathies Supplemental material is available for this article. © RSNA, 2023.
Keyphrases
- heart failure
- left ventricular
- cardiac resynchronization therapy
- contrast enhanced
- atrial fibrillation
- magnetic resonance imaging
- blood pressure
- acute myocardial infarction
- left atrial
- skeletal muscle
- magnetic resonance
- pulmonary hypertension
- subarachnoid hemorrhage
- mitral valve
- coronary artery disease
- antiretroviral therapy
- brain injury
- acute coronary syndrome