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An unusual cause of acute renal failure in sickle cell disease
A young female with sickle cell disease was treated for biopsy-proven IgA nephropathy. Serum creatinine levels resolved to normal range, but a year later, she presented with oedema, hypertension and acute renal failure. A repeat renal biopsy showed acute-on-chronic thrombotic microangiopathy (TMA)....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421385/ https://www.ncbi.nlm.nih.gov/pubmed/25949348 http://dx.doi.org/10.1093/ndtplus/sfp081 |
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author | Rockx, Marie-Antoinette Gibson, Ian W. Reslerova, Martina |
author_facet | Rockx, Marie-Antoinette Gibson, Ian W. Reslerova, Martina |
author_sort | Rockx, Marie-Antoinette |
collection | PubMed |
description | A young female with sickle cell disease was treated for biopsy-proven IgA nephropathy. Serum creatinine levels resolved to normal range, but a year later, she presented with oedema, hypertension and acute renal failure. A repeat renal biopsy showed acute-on-chronic thrombotic microangiopathy (TMA). We suggest that circulating microparticles could be a pathophysiological link between sickle cell disease and the development of renal TMA. This case emphasizes the importance of a further biopsy for acutely declining renal function, even when a definite diagnosis has been made from a previous biopsy. |
format | Online Article Text |
id | pubmed-4421385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44213852015-05-06 An unusual cause of acute renal failure in sickle cell disease Rockx, Marie-Antoinette Gibson, Ian W. Reslerova, Martina NDT Plus Case Report A young female with sickle cell disease was treated for biopsy-proven IgA nephropathy. Serum creatinine levels resolved to normal range, but a year later, she presented with oedema, hypertension and acute renal failure. A repeat renal biopsy showed acute-on-chronic thrombotic microangiopathy (TMA). We suggest that circulating microparticles could be a pathophysiological link between sickle cell disease and the development of renal TMA. This case emphasizes the importance of a further biopsy for acutely declining renal function, even when a definite diagnosis has been made from a previous biopsy. Oxford University Press 2009-10 2009-07-22 /pmc/articles/PMC4421385/ /pubmed/25949348 http://dx.doi.org/10.1093/ndtplus/sfp081 Text en © The Author [2009]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Report Rockx, Marie-Antoinette Gibson, Ian W. Reslerova, Martina An unusual cause of acute renal failure in sickle cell disease |
title | An unusual cause of acute renal failure in sickle cell disease |
title_full | An unusual cause of acute renal failure in sickle cell disease |
title_fullStr | An unusual cause of acute renal failure in sickle cell disease |
title_full_unstemmed | An unusual cause of acute renal failure in sickle cell disease |
title_short | An unusual cause of acute renal failure in sickle cell disease |
title_sort | unusual cause of acute renal failure in sickle cell disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421385/ https://www.ncbi.nlm.nih.gov/pubmed/25949348 http://dx.doi.org/10.1093/ndtplus/sfp081 |
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