Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle
disease, which is characterized by fibro-fatty replacement of predominantly the right ventricle …

Objective The purpose of this article is to review how cardiac MRI provides the clinician with
detailed information about the hypertrophic cardiomyopathy (HCM) phenotypes, assessing …

Cardiac magnetic resonance imaging (CMR) is a useful technique in the evaluation of
patients with suspected or diagnosed hypertrophic cardiomyopathy (HCM), and has an …

Background and Aims. Cardiac outpouchings encounter a series of distinct congenital or
acquired entities (ie aneurysms, pseudoaneurysms, diverticula, and herniations), whose …

A pouch protruding into the wall of the left ventricle (LV) may be either a recess, cleft,
diverticulum, or aneurysm. Being aware of these anomalies is essential to make accurate …

Hypertrophic cardiomyopathy (HCM) is characterized by left ventricular hypertrophy (LVH) in
the absence of another causal disease. Several morphologic and histologic changes have …

Cardiac ventricular outpouchings and invaginations are rare structural abnormalities and
usually incidental findings during cardiac imaging. A definitive diagnosis is possible through …

Background Myocardial infarction-related left ventricular pseudoaneurysm (LVP), covered
by the adjacent pericardial or scar tissue, is a fatal sequela of left ventricular rupture …

Numerous entities, both structural and pathologic, can manifest as a contrast material–or
blood-filled cardiac outpouching at imaging. These outpouchings often resemble one …

Objective Myocardial crypts are congenital abnormalities associated with hypertrophic
cardiomyopathy (HCM) and other conditions. This study assessed the prevalence of …