Cardiac sarcoidosis with multiple left ventricular aneurysms (LVAs) in a young male

Abstract

Multiple left ventricular aneurysms (LVAs) are distinctly rare and have varied etiology. Manifestations of these entities are similar to the commonest LVA of ischemic origin. Our case is a young male with multiple LVAs with histological evidence of chronic granulomatous disease, and cardiac imaging suggestive of sarcoidosis, responded well to immunosuppressive therapy.