Cargando…
Diagnosis and Management of a Cardiac Amyloidosis Case Mimicking Hypertrophic Cardiomyopathy
Cardiac amyloidosis is an acquired heart disease secondary to the deposition of β-pleated amyloid proteins in heart tissue. Amyloid light chain (AL) amyloidosis is usually secondary to multiple myeloma and can rapidly deteriorate cardiac function, with high mortality. Up to 50% of AL patients have c...
Autores principales: | Sattar, Yasar, Ruiz Maya, Tania, Zafrullah, Fnu, Patel, Nirav B, Latchana, Sharaad |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388819/ https://www.ncbi.nlm.nih.gov/pubmed/30820370 http://dx.doi.org/10.7759/cureus.3749 |
Ejemplares similares
-
Ivabradine in Congestive Heart Failure: Patient Selection and Perspectives
por: Sattar, Yasar, et al.
Publicado: (2019) -
Cardiac amyloidosis and hypertrophic cardiomyopathy: A dangerous liaison
por: Ebrille, Elisa, et al.
Publicado: (2013) -
Amyloidosis with phenotype of hypertrophic cardiomyopathy
por: Kuryła, Martyna, et al.
Publicado: (2023) -
Pheochromocytoma and Hypertrophic Cardiomyopathy Leading to Cardiac Arrest
por: Niu, Kevyn, et al.
Publicado: (2023) -
Association of Hypertrophic Obstructive Cardiomyopathy with Rheumatoid Arthritis
por: Dawood, Mustafa, et al.
Publicado: (2018)