Myocardial inflammation detected by cardiac MRI in Arrhythmogenic right ventricular cardiomyopathy: A paediatric case series

Int J Cardiol. 2018 Nov 15:271:81-86. doi: 10.1016/j.ijcard.2018.05.116. Epub 2018 May 31.

Abstract

Introduction: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited myocardial disease with an elusive association with myocardial inflammation. A myocarditis phenotype has been well established without systematic evidence of a viral trigger. We intend to study the relationship between myocardial inflammation detected by Cardiac magnetic resonance (CMR) and ARVC in a paediatric population.

Methods: Retrospective case series of all patients <18 years admitted to two CMR units for clinical suspicion of myocarditis from March 2012 to June 2017 who had genetic testing for inherited cardiomyopathies including analysis for known ARVC genes.

Results: Six patients were identified experiencing myocarditis-like episodes with chest pain and troponin elevation. All had CMR evidence of active myocardial inflammation often affecting the left ventricle without identification of an infectious trigger. These episodes were likely exercise-induced in 50% of our patients and were multiple in all but one.

Conclusion: We provide evidence that ARVC can present as recurrent myocarditis-like episodes with CMR evidence of myocardial inflammation despite absent infectious trigger in children. We believe they represent an active hot phase of the disease and may lead to disease progression.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Arrhythmogenic Right Ventricular Dysplasia / complications*
  • Arrhythmogenic Right Ventricular Dysplasia / diagnostic imaging*
  • Arrhythmogenic Right Ventricular Dysplasia / physiopathology
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Magnetic Resonance Imaging, Cine / methods*
  • Male
  • Myocarditis / complications*
  • Myocarditis / diagnostic imaging*
  • Myocarditis / physiopathology
  • Retrospective Studies