Diagnostic Challenges in Rare Causes of Arrhythmogenic Cardiomyopathy-The Role of Cardiac MRI.
Simona ManoleRoxana PinticanGeorge PopaRaluca RanceaAlexandra Dădârlat-PopRomana VulturarEmanuel PaladePublished in: Journal of personalized medicine (2022)
Arrhythmogenic right ventricular dysplasia (ARVD) is a rare genetic condition of the myocardium, with a significantly high risk of sudden death. Recent genetic research and improved understanding of the pathophysiology tend to change the ARVD definition towards a larger spectrum of myocardial involvement, which includes, in various proportions, both the right (RV) and left ventricle (LV), currently referred to as ACM (arrhythmogenic cardiomyopathy). Its pathological substrate is defined by the replacement of the ventricular myocardium with fibrous adipose tissue that further leads to inadequate electrical impulses and translates into varies degrees of malignant ventricular arrythmias and dyskinetic myocardium movements. Particularly, the cardio-cutaneous syndromes of Carvajal/Naxos represent rare causes of ACM that might be suspected from early childhood. The diagnostic is sometimes challenging, even with well-established rTFC or Padua criteria, especially for pediatric patients or ACM with LV involvement. Cardiac MRI gain more and more importance in ACM diagnostic especially in non-classical forms. Furthermore, MRI is useful in highlighting myocardial fibrosis, fatty replacement or wall movement with high accuracy, thus guiding not only the depiction, but also the patient's stratification and management.
Keyphrases
- left ventricular
- heart failure
- contrast enhanced
- magnetic resonance imaging
- adipose tissue
- diffusion weighted imaging
- mitral valve
- genome wide
- computed tomography
- insulin resistance
- high fat diet
- cerebral palsy
- pulmonary artery
- type diabetes
- case report
- catheter ablation
- skeletal muscle
- pulmonary arterial hypertension
- coronary artery
- liver fibrosis