Arrhythmogenic left ventricular cardiomyopathy mimicking acute myocardial infarction
Cen-Cen WU1
Le-Qun ZHOU2
Xin-Yu WANG2
Ling-Yun ZU2
Wei-Xian XU2
1.Department of Cardiology and Institute of Vascular Medicine,Peking University Third Hospital,Beijing,China;State Key Laboratory of Vascular Homeostasis and Remodeling,Peking University,Beijing,China2.Department of Cardiology and Institute of Vascular Medicine,Peking University Third Hospital,Beijing,China;State Key Laboratory of Vascular Homeostasis and Remodeling,Peking University,Beijing,China;NHC Key Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides,Peking University,Beijing,China;Beijing Key Laborat-ory of Cardiovascular Receptors Research,Beijing,China
摘要：Arrhythmogenic cardiomyopathy(ACM),also known as hereditary cardiomyopathy,is characterized by a gradual loss of cardio-myocytes,which are replaced by fibrous or fibrofatty tis-sues.The disease was initially designated as arrhythmo-genic right ventricular cardiomyopathy,which predis-posed to fatal ventricular arrhythmias and sudden car-diac death.[1,2]However,recent insights in autopsy in-vestigations,genotype-phenotype correlation studies,and myocardial tissue characterization by cardiac mag-netic resonance(CMR)have broadened our underst-anding of the disease,revealing that it frequently invo-lves the left ventricle(LV).
机标关键词：acutearrhythmogeniccardiomyopathyinfarctionleftmimickingmyocardialventricular
论文发表日期：2024-12-28
在线出版日期：2025-08-15（本平台首次上网日期，不代表文献的发表时间）
页数：6( 1141-1146 )