CARDIAC HAMARTOMA MASQUERADING AS HYPERTROPHIC CARDIOMYOPATHY

Cardiac hamartomas are exceedingly rare. They can manifest with dyspnea, chest pain, sudden death, peripheral embolism or ventricular arrhythmia. A 36 year old male with a history of a cardiac mass resected from the RVOT (right ventricular outflow tract) at age 3 presents with exertional dyspnea