Hypertrophic cardiomyopathy in the systemic right ventricle in a patient with congenitally corrected transposition of the great arteries: A case report

Author:

García‐Cruz Edgar1,Manzur‐Sandoval Daniel2ORCID,Toledo‐Alemán Enma Leticia3,Angulo‐Cruzado Stephanie Teresa1,Sánchez‐López Sheila Vania1,Benita‐Bordes Antonio4,Calderón‐Colmenero Juan1,Díaz‐Gallardo Linda Guieniza1,Aranda‐Fraustro Alberto5,Mata‐Salgado Gabriela Denisse1,Baranda‐Tovar Francisco Martín6

Affiliation:

1. Congenital Heart Disease Unit Instituto Nacional de Cardiología Ignacio Chávez Mexico City Mexico

2. Cardiovascular Critical Care Unit Instituto Nacional de Cardiología Ignacio Chávez Mexico City Mexico

3. Cardiology Department Instituto Nacional de Cardiología Ignacio Chávez Mexico City Mexico

4. Congenital Heart Disease Surgery Department Instituto Nacional de Cardiología Ignacio Chávez Mexico City Mexico

5. Patology Department Instituto Nacional de Cardiología Ignacio Chávez Mexico City Mexico

6. Surgical and Medical Specialties Direction Instituto Nacional de Cardiología Ignacio Chávez Mexico City Mexico

Abstract

AbstractCongenitally corrected transposition of the great arteries is a rare clinical entity, which usually presents during adulthood with associated defects; atrioventricular block, heart failure, systemic valve failure, and arrhythmias usually complicate the clinical course. Even rarer is associated hypertrophic cardiomyopathy, which complicates the disease course and clinical decision‐making. Herein, we present a patient with this condition who underwent heart transplantation, with adequate clinical resolution.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging

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