Isolated right ventricular hypertrophic cardiomyopathy presented in a 13-year-old male, mimicking an intramural mass and necessitating advanced imaging for diagnosis.
Isolated right ventricular outflow tract hypertrophic cardiomyopathy can mimic an intramural mass on imaging and should be considered in the differential diagnosis for adolescents with exertional dyspnea.
Absolute Event Rate: 0% vs 0%
ABSTRACT Hypertrophic cardiomyopathy (HCM) primarily involves the left ventricle, with severe right ventricular hypertrophy or right ventricular outflow tract (RVOT) obstruction being rare. Hypertrophic myocardium may mimic intramural masses, requiring imaging, intraoperative observation and pathological examination for diagnosis. Here, we present a case of RVOT‐type HCM.
Tingting et al. (Thu,) reported a other. Isolated right ventricular hypertrophic cardiomyopathy presented in a 13-year-old male, mimicking an intramural mass and necessitating advanced imaging for diagnosis.