Magnetic resonance imaging assessment of arrhythmogenic right ventricular cardiomyopathy/dysplasia in children

Shi Joon Yoo, Lars Grosse-Wortmann, Robert M. Hamilton

Research output: Contribution to journalReview articlepeer-review

12 Scopus citations

Abstract

Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a genetically determined disease that progresses continuously from conception and throughout life. ARVC/D manifests predominantly in young adulthood. Early identification of the concealed cases in childhood is of utmost importance for the prevention of sudden cardiac death later in life. Magnetic resonance imaging (MRI) is routinely requested in patients with a confirmed or suspected diagnosis of ARVC/D and in family members of the patients with ARVC/D. Although the utility of MRI in the assessment of ARVC/D is well recognized in adults, MRI is a low-yield test in children as the anatomical, histological, and functional changes are frequently subtle or not present in the early phase of the disease. MRI findings of ARVC/D include morphologic changes such as right ventricular dilatation, wall thinning, and aneurismal outpouchings, as well as abnormal tissue characteristics such as myocardial fibrosis and fatty infiltration, and functional abnormalities such as global ventricular dysfunction and regional wall motion abnormalities. Among these findings, regional wall motion abnormalities are the most reliable MRI findings both in children and adults, while myocardial fibrosis and fat infiltration are rarely seen in children. Therefore, an MRI protocol should be tailored according to the patients age and compliance, as well as the presence of other findings, instead of using the protocol that is used for adults. We propose that MRI in children with ARVC/D should focus on the detection of regional wall motion abnormalities and global ventricular function by using a cine imaging sequence and that the sequences for myocardial fat and late gadolinium enhancement of the myocardium are reserved for those who show abnormal findings at cine imaging. Importandy, MRI should be performed and interpreted by experienced examiners to reduce the number of false positive and false negative readings.

Original languageEnglish (US)
Pages (from-to)357-367
Number of pages11
JournalKorean Circulation Journal
Volume40
Issue number8
DOIs
StatePublished - Aug 2010
Externally publishedYes

Keywords

  • Arrhythmogenic right ventricular cardiomyopathy/dysplasia
  • Children
  • Magnetic resonance imaging

ASJC Scopus subject areas

  • Internal Medicine
  • Cardiology and Cardiovascular Medicine

Fingerprint Dive into the research topics of 'Magnetic resonance imaging assessment of arrhythmogenic right ventricular cardiomyopathy/dysplasia in children'. Together they form a unique fingerprint.

Cite this