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Biventricular arrhythmogenic cardiomyopathy diagnosed in a young patient: A case report with literature review

Arrhythmogenic cardiomyopathy is a genetic heart muscle disease that typically affects the right ventricle. However, 2 other phenotypes affecting the left ventricle were recently discovered. Here, we report the case of an 18-year-old patient with biventricular arrhythmogenic cardiomyopathy, highligh...

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Detalles Bibliográficos
Autores principales: El Ouartassi, Hajar, Faraj, Raid, Laraichi, Zakariae, Ezzahraoui, Rhita, Bourouhou, Zaineb, Doghmi, Nawal, Cherti, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375373/
https://www.ncbi.nlm.nih.gov/pubmed/37520387
http://dx.doi.org/10.1016/j.radcr.2023.06.034
Descripción
Sumario:Arrhythmogenic cardiomyopathy is a genetic heart muscle disease that typically affects the right ventricle. However, 2 other phenotypes affecting the left ventricle were recently discovered. Here, we report the case of an 18-year-old patient with biventricular arrhythmogenic cardiomyopathy, highlighting the challenges encountered in establishing this diagnosis. Diagnostic criteria for the left-sided phenotypic variants of arrhythmogenic cardiomyopathy were only introduced in 2020 by an international expert consensus document, known as the “Padua criteria,” they are divided in 6 categories with an emphasis on morpho-functional ventricular abnormalities and structural myocardial tissue alterations to diagnose biventricular arrhythmogenic cardiomyopathy.