Amyloidosis – short review

Bibliographic Details
Title: Amyloidosis – short review
Authors: Agnieszka Danuta Gaczkowska, Paweł Jagodziński, Adrianna Mostowska
Source: Journal of Medical Science, Vol 85, Iss 2 (2016)
Publisher Information: Poznan University of Medical Sciences, 2016.
Publication Year: 2016
Collection: LCC:Medicine
Subject Terms: amyloidosis, amyloid, diagnostic, treatment, Medicine
More Details: Amyloidosis is a heterogeneous group of disorders associated with pathological deposition of amyloid. We can recognize two major categories of amyloidosis: primary (AL) and secondary (AA) type. Systemic monoclonal immunoglobulin light-chain (AL) is the most common form of systemic amyloidosis. Systemic AA amyloidosis is associated with chronic inflammation or infective diseases and is the second common form of systemic amyloidosis. The golden standard in diagnosis of amyloidosis is biopsy. The model of treatment depends of type of amyloidosis. In some cases there is considerate cell transplantation. In AA the purpose is to decrease inflammation.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2353-9798
2353-9801
Relation: https://jms.ump.edu.pl/index.php/JMS/article/view/101; https://doaj.org/toc/2353-9798; https://doaj.org/toc/2353-9801
DOI: 10.20883/jms.2016.101
Access URL: https://doaj.org/article/92122245901d4b969ada30f0d9c72f6c
Accession Number: edsdoj.92122245901d4b969ada30f0d9c72f6c
Database: Directory of Open Access Journals
More Details
ISSN:23539798
23539801
DOI:10.20883/jms.2016.101
Published in:Journal of Medical Science
Language:English