Cardiac Amyloidosis Masked as Hypertrophic Cardiomyopathy: A Case Report

It is well known that cardiac amyloidosis and hypertrophic cardiomyopathy (HCM) have different physiologies and pathologies. However, it might be difficult to differentiate cardiac amyloidosis from HCM in certain clinical situations.

Detalles Bibliográficos
Autores principales: Wang, Jing, Marzolf, Amy, Zhang, Janet C. L., Owens, Anjali, Han, Yuchi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295565/
https://www.ncbi.nlm.nih.gov/pubmed/28197289
http://dx.doi.org/10.14740/cr496w
Descripción
Sumario:It is well known that cardiac amyloidosis and hypertrophic cardiomyopathy (HCM) have different physiologies and pathologies. However, it might be difficult to differentiate cardiac amyloidosis from HCM in certain clinical situations.

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