Arrhythmogenic Right Ventricular Cardiomyopathy Underlies Syndrome of Right Bundle Branch Block, ST-Segment Elevation, and Sudden Death

Right ventricular morphologic and/or histologic abnormalities were present in 5 of 6 Japanese men with the Brugada syndrome. Results indicate that arrhythmogenic right ventricular cardiomyopathy may underlie the cardiac manifestations in the Brugada syndrome.

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Veröffentlicht in:The American journal of cardiology 1998-02, Vol.81 (4), p.519-522
Hauptverfasser: Tada, Hiroshi, Aihara, Naohiko, Ohe, Tohru, Yutani, Chikao, Hamada, Seiki, Miyanuma, Hiroaki, Takamiya, Makoto, Kamakura, Shiro
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container_end_page 522
container_issue 4
container_start_page 519
container_title The American journal of cardiology
container_volume 81
creator Tada, Hiroshi
Aihara, Naohiko
Ohe, Tohru
Yutani, Chikao
Hamada, Seiki
Miyanuma, Hiroaki
Takamiya, Makoto
Kamakura, Shiro
description Right ventricular morphologic and/or histologic abnormalities were present in 5 of 6 Japanese men with the Brugada syndrome. Results indicate that arrhythmogenic right ventricular cardiomyopathy may underlie the cardiac manifestations in the Brugada syndrome.
doi_str_mv 10.1016/S0002-9149(97)00942-9
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Adult
Biological and medical sciences
Bundle-Branch Block - etiology
Cardiac dysrhythmias
Cardiology
Cardiology. Vascular system
Cardiomyopathies - complications
Cardiomyopathies - diagnostic imaging
Cardiomyopathies - pathology
Cardiovascular disease
Death, Sudden, Cardiac - etiology
Electrocardiography
Heart
Heart Ventricles - diagnostic imaging
Heart Ventricles - pathology
Humans
Male
Medical sciences
Middle Aged
Retrospective Studies
Syndrome
Tomography, X-Ray Computed
Ventricular Fibrillation - etiology
title Arrhythmogenic Right Ventricular Cardiomyopathy Underlies Syndrome of Right Bundle Branch Block, ST-Segment Elevation, and Sudden Death
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