Rapidly Progressive Apical Hypertrophic Cardiomyopathy: Not Everything is What It Seems
Abstract
Apical hypertrophic cardiomyopathy (HCM) is a rare variant of HCM. A 43-year-old female with a past medical history significant for hypertension and kidney transplantation presented with recurrent syncopal episodes and dyspnea on exertion. Electrocardiogram showed characteristic diffuse giant T-waves inversion, and cardiac magnetic resonance showed HCM with circumferential apical thickening. This case highlights the rapid development of apical HCM and its challenging diagnostic characteristics.
© 2024 Ahmed K. Mahmoud, Juan M. Farina, Kamal Awad, Milagros Pereyra, Isabel G. Scalia, Mohammed Tiseer Abbas, Timothy Barry, Said Alsidawi, Chadi Ayoub, Reza Arsanjani, published by Houston Methodist DeBakey Heart & Vascular Center
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