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Cardiac amyloidosis—An underdiagnosed cause of heart failure: A case report and review of literature

Restrictive cardiomyopathy secondary to cardiac amyloidosis is an underdiagnosed, but treatable, cause of heart failure involving an extracellular deposition of misfolded protein. Hereby, we report a case of a female patient with history of nephrotic syndrome for 1 year who subsequently presented wi...

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Detalles Bibliográficos
Autores principales: Parmar, Kanak, Benjanuwattra, Juthipong, Sethi, Pooja, Tijani, Lukman, Hurst, Philip, Pertuz, Gaspar Del‐Rio, Argueta‐Sosa, Erwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718913/
https://www.ncbi.nlm.nih.gov/pubmed/36478969
http://dx.doi.org/10.1002/ccr3.6525
Descripción
Sumario:Restrictive cardiomyopathy secondary to cardiac amyloidosis is an underdiagnosed, but treatable, cause of heart failure involving an extracellular deposition of misfolded protein. Hereby, we report a case of a female patient with history of nephrotic syndrome for 1 year who subsequently presented with symptoms of heart failure. The findings on cardiac imaging supported the suspicion of cardiac amyloidosis. Further laboratory workup for amyloidosis was pursued along with endomyocardial biopsy which confirmed amyloidosis‐AL type. Patient was started on chemotherapy. The case underscores the importance of a timely diagnosis with the help of symptomatology and imaging along with a multidisciplinary approach for patient care.