Primary systemic amyloidosis as a real diagnostic challenge – case study

Primary amyloidosis (AL) is a rare variety of plasma cell dyscrasia, the diagnosis of which is often difficult to establish. Pathogenesis of amyloidosis involves extracellular deposition of insoluble protein fibrils in tissues, leading to insufficiency of affected organs. According to various source...

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Detalles Bibliográficos
Autores principales: Jerzykowska, Sonia, Cymerys, Maciej, Gil, Lidia A., Balcerzak, Andrzej, Pupek-Musialik, Danuta, Komarnicki, Mieczysław A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2014
Materias:
Case Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439975/
https://www.ncbi.nlm.nih.gov/pubmed/26155101
http://dx.doi.org/10.5114/ceji.2014.42126

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439975/
https://www.ncbi.nlm.nih.gov/pubmed/26155101
http://dx.doi.org/10.5114/ceji.2014.42126

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