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

被引：0

作者：

Garcia-Cruz, Edgar ^{[1
]}

Manzur-Sandoval, Daniel ^{[2
,7
]}

Toledo-Aleman, Enma Leticia ^{[3
]}

Angulo-Cruzado, Stephanie Teresa ^{[1
]}

Sanchez-Lopez, Sheila Vania ^{[1
]}

Benita-Bordes, Antonio ^{[4
]}

Calderon-Colmenero, Juan ^{[1
]}

Diaz-Gallardo, Linda Guieniza ^{[1
]}

Aranda-Fraustro, Alberto ^{[5
]}

Mata-Salgado, Gabriela Denisse ^{[1
]}

Baranda-Tovar, Francisco Martin ^{[6
]}

机构：

[1] Inst Nacl Cardiol Ignacio Chavez, Congenital Heart Dis Unit, Mexico City, Mexico

[2] Inst Nacl Cardiol Ignacio Chavez, Cardiovasc Crit Care Unit, Mexico City, Mexico

[3] Inst Nacl Cardiol Ignacio Chavez, Cardiol Dept, Mexico City, Mexico

[4] Inst Nacl Cardiol Ignacio Chavez, Congenital Heart Dis Surg Dept, Mexico City, Mexico

[5] Inst Nacl Cardiol Ignacio Chavez, Patol Dept, Mexico City, Mexico

[6] Inst Nacl Cardiol Ignacio Chavez, Surg & Med Specialties Direct, Mexico City, Mexico

[7] Inst Nacl Cardiol Ignacio Chavez, Cardiovasc Crit Care Unit, Juan Badiano 1,Belisario Dominguez Secc 16,PO 1408, Mexico City, Mexico

来源：

ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES | 2023年 / 40卷 / 09期

关键词：

cardiac transplantation; congenital heart disease; congenitally corrected transposition of the great arteries; OBSTRUCTION; OUTFLOW;

D O I：

10.1111/echo.15660

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

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.

引用

页码：1016 / 1020

页数：5

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