A case of arrhythmogenic right ventricular cardiomyopathy with right ventricle thrombus: A case report.
Med J Malaysia
; 75(4): 452-454, 2020 07.
Article
en En
| MEDLINE
| ID: mdl-32724017
ABSTRACT
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare inherited cardiomyopathy characterised by right ventricular dysfunction, ventricular arrhythmias and increased risk of sudden cardiac death. Due to the replacement of myocardium with fibro-fatty and fibrous tissue, patients with ARVC are prone to develop ventricular tachycardia. Histologically, it is often reported as the 'triangle of dysplasia' involving the inflow tract, outflow tract and apex of the right ventricle.2 We describe a 20-years-old patient who collapsed during a futsal match and was subsequently diagnosed to have ARVC with a right ventricular thrombus from cardiac magnetic resonance imaging.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Trombosis
/
Disfunción Ventricular Derecha
/
Displasia Ventricular Derecha Arritmogénica
Límite:
Adult
/
Humans
/
Male
Idioma:
En
Revista:
Med J Malaysia
Año:
2020
Tipo del documento:
Article
País de afiliación:
Malasia