咨询与建议

看过本文的还看了

相关文献

该作者的其他文献

文献详情 >Congenitally Corrected Transpo... 收藏

Congenitally Corrected Transposition of the Great Arteries: Conduction Anomalies: A Case Report

Congenitally Corrected Transposition of the Great Arteries: Conduction Anomalies: A Case Report

作     者:Jose Antonio Luna-Alvarez-Amezquita Javier Ivan Armenta-Moreno Joaquin Berarducci Jorge Luis Bermudez-Gonzalez Jose Luis Siller-Nava Edson Alberto Escandón-Villalobos Nilda Espinola-Zavaleta Roberto Cano-Zarate Juan Ignacio Straface Jose Antonio Luna-Alvarez-Amezquita;Javier Ivan Armenta-Moreno;Joaquin Berarducci;Jorge Luis Bermudez-Gonzalez;Jose Luis Siller-Nava;Edson Alberto Escandón-Villalobos;Nilda Espinola-Zavaleta;Roberto Cano-Zarate;Juan Ignacio Straface

作者机构:Department of Nuclear Cardiology National Institute of Cardiology Ignacio Chavez Mexico City Mexico Department of Echocardiography ABC Medical Center I.A.P. Mexico City Mexico Department of Magnetic Resonance National Institute of Cardiology Ignacio Chavez Mexico City Mexico 

出 版 物:《World Journal of Cardiovascular Diseases》 (心血管病(英文))

年 卷 期:2021年第11卷第9期

页      面:439-444页

学科分类:1002[医学-临床医学] 100201[医学-内科学(含:心血管病、血液病、呼吸系病、消化系病、内分泌与代谢病、肾病、风湿病、传染病)] 10[医学] 

主  题:Congenital Heart Disease Congenitally Corrected Transposition of the Great Arteries Cardiac Magnetic Resonance Echocardiography Arrhythmia 

摘      要:Introduction: Congenitally corrected transposition of the great arteries (CCTGA) is a rare heart disease that encompasses an atrioventricular and ventriculoarterial discordance and accounts for less than 1 percent of congenital heart diseases. Objective: To present an atypical case of a man with complex congenital heart disease and conduction anomalies. Case Presentation: This is a case of a 34-year-old patient who came to the hospital with 1 week of dyspnea on exertion and episodes of lipothymia. The patient was referred to our hospital after an electrocardiogram from his primary care with evidence of blocked atrial fibrillation. During the initial evaluation blocked atrial fibrillation was confirmed with a rescue ventricular rate of 38 bpm. A magnetic resonance confirmed the presence of the atrioventricular and ventriculoarterial discordance, the aorta had a left anterior position, perimembranous ventricular septal defect with a right to left shunt, biventricular systolic dysfunction, moderate tricuspid, and mitral regurgitation, interventricular septal intramyocardial and biatrial fibrosis, left atrial dilation, and dilation of the pulmonary artery. After pacemaker placement, the patient has an improvement in his clinical symptoms and quality of life. Conclusions: Cardiac arrhythmias are CCTGA’s leading cause of death, mostly ventricular tachycardia, and atrial fibrillation. Right bundle branch block is a previously unreported and potentially very rare presentati

读者评论 与其他读者分享你的观点

用户名:未登录
我的评分