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Amyloid A amyloidosis with subcutaneous drug abuse
Introduction: Amyloid A (AA) amyloidosis is a systemic form of amyloidosis secondary to chronic infections and inflammatory disorders. An acute-phase protein produced by the liver, serum amyloid A (SAA) is the precursor of AA amyloid fibrils. AA amyloid deposition occurs predominantly in the kidneys...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nickan Research Institute
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206034/ https://www.ncbi.nlm.nih.gov/pubmed/25340157 http://dx.doi.org/10.12861/jrip.2014.06 |
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author | Mendoza, Jair Munoz Peev, Vasil Ponce, Mario A Thomas, David B Nayer, Ali |
author_facet | Mendoza, Jair Munoz Peev, Vasil Ponce, Mario A Thomas, David B Nayer, Ali |
author_sort | Mendoza, Jair Munoz |
collection | PubMed |
description | Introduction: Amyloid A (AA) amyloidosis is a systemic form of amyloidosis secondary to chronic infections and inflammatory disorders. An acute-phase protein produced by the liver, serum amyloid A (SAA) is the precursor of AA amyloid fibrils. AA amyloid deposition occurs predominantly in the kidneys, spleen, adrenal glands, liver and gastrointestinal tract. The manifestations of AA amyloidosis involving the kidneys include proteinuria, tubular dysfunction and progressive loss of renal function. Case: We report a 47-year-old drug addict who developed AA amyloidosis as a result of recurrent suppurative skin infections secondary to subcutaneous drug injection. Elevated C-reactive protein concentrations attested to the presence of a chronic systemic inflammatory state. He suffered from the nephrotic syndrome and insidious loss of renal function. Isosthenuria and glycosuria were indicative of renal tubular dysfunction. Renal biopsy demonstrated AA amyloidosis involving the glomeruli, tubular basement membranes and blood vessel walls. Conclusion: Superimposed acute tubular necrosis due to concomitant endocarditis and cocaine use accelerated his renal disease. Case presentation is followed by a brief discussion of clinical features, natural history and outcome of AA amyloidosis with a particular emphasis on AA amyloidosis as a complication of subcutaneous drug abuse. |
format | Online Article Text |
id | pubmed-4206034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nickan Research Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-42060342014-10-22 Amyloid A amyloidosis with subcutaneous drug abuse Mendoza, Jair Munoz Peev, Vasil Ponce, Mario A Thomas, David B Nayer, Ali J Renal Inj Prev Case Report Introduction: Amyloid A (AA) amyloidosis is a systemic form of amyloidosis secondary to chronic infections and inflammatory disorders. An acute-phase protein produced by the liver, serum amyloid A (SAA) is the precursor of AA amyloid fibrils. AA amyloid deposition occurs predominantly in the kidneys, spleen, adrenal glands, liver and gastrointestinal tract. The manifestations of AA amyloidosis involving the kidneys include proteinuria, tubular dysfunction and progressive loss of renal function. Case: We report a 47-year-old drug addict who developed AA amyloidosis as a result of recurrent suppurative skin infections secondary to subcutaneous drug injection. Elevated C-reactive protein concentrations attested to the presence of a chronic systemic inflammatory state. He suffered from the nephrotic syndrome and insidious loss of renal function. Isosthenuria and glycosuria were indicative of renal tubular dysfunction. Renal biopsy demonstrated AA amyloidosis involving the glomeruli, tubular basement membranes and blood vessel walls. Conclusion: Superimposed acute tubular necrosis due to concomitant endocarditis and cocaine use accelerated his renal disease. Case presentation is followed by a brief discussion of clinical features, natural history and outcome of AA amyloidosis with a particular emphasis on AA amyloidosis as a complication of subcutaneous drug abuse. Nickan Research Institute 2013-11-02 /pmc/articles/PMC4206034/ /pubmed/25340157 http://dx.doi.org/10.12861/jrip.2014.06 Text en Copyright © 2014 The Author(s); Published by Nickan Research Institute http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Mendoza, Jair Munoz Peev, Vasil Ponce, Mario A Thomas, David B Nayer, Ali Amyloid A amyloidosis with subcutaneous drug abuse |
title | Amyloid A amyloidosis with subcutaneous drug abuse |
title_full | Amyloid A amyloidosis with subcutaneous drug abuse |
title_fullStr | Amyloid A amyloidosis with subcutaneous drug abuse |
title_full_unstemmed | Amyloid A amyloidosis with subcutaneous drug abuse |
title_short | Amyloid A amyloidosis with subcutaneous drug abuse |
title_sort | amyloid a amyloidosis with subcutaneous drug abuse |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206034/ https://www.ncbi.nlm.nih.gov/pubmed/25340157 http://dx.doi.org/10.12861/jrip.2014.06 |
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