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

Autor: García-Cruz E; Congenital Heart Disease Unit, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico., Manzur-Sandoval D; Cardiovascular Critical Care Unit, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico., Toledo-Alemán EL; Cardiology Department, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico., Angulo-Cruzado ST; Congenital Heart Disease Unit, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico., Sánchez-López SV; Congenital Heart Disease Unit, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico., Benita-Bordes A; Congenital Heart Disease Surgery Department, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico., Calderón-Colmenero J; Congenital Heart Disease Unit, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico., Díaz-Gallardo LG; Congenital Heart Disease Unit, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico., Aranda-Fraustro A; Patology Department, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico., Mata-Salgado GD; Congenital Heart Disease Unit, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico., Baranda-Tovar FM; Surgical and Medical Specialties Direction, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Jazyk: angličtina
Zdroj: Echocardiography (Mount Kisco, N.Y.) [Echocardiography] 2023 Sep; Vol. 40 (9), pp. 1016-1020. Date of Electronic Publication: 2023 Jul 27.
DOI: 10.1111/echo.15660
Abstrakt: Congenitally 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.
(© 2023 Wiley Periodicals LLC.)
Databáze: MEDLINE
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