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Primary cardiac amyloidosis

Authors :
A. Yu. Kraposhina
I. A. Soloveva
Irina Demko
V. A. Mosina
N. V. Gordeeva
L. I. Pelinovskaya
Source :
Clinical Medicine (Russian Journal). 95:971-976
Publication Year :
2018
Publisher :
Medical Informational Agency Publishers, 2018.

Abstract

Cardiac amyloidosis - the disease which is characterized by deposition of insoluble protein amyloid in intercellular space is one of the most severe implications of systemic amyloidosis. Primary cardiac amyloidosis possesses a wide range of clinical implications that complicates well-timed diagnostics and, respectively, treatment. The long latent current and the adverse forecast do extremely important diagnostics of cardiac amyloidosis at early stages of a disease. The modern concept of pathogenesis and morphology of an amyloidosis is covered in article, the clinical options of a current, diagnostic methods of dysfunction of heart including bio- and immunochemical blood analysis and urine, a complex of tool methods of a research and «the gold standard» of verification of deposits of amyloid - a biopsy of various organs and tissues are described.

Details

ISSN :
24121339 and 00232149
Volume :
95
Database :
OpenAIRE
Journal :
Clinical Medicine (Russian Journal)
Accession number :
edsair.doi...........5d31e949eb528a70becd41ca027c5f9e
Full Text :
https://doi.org/10.18821/0023-2149-2017-95-11-971-976