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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)....

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Detalles Bibliográficos
Autores principales: Rockx, Marie-Antoinette, Gibson, Ian W., Reslerova, Martina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2009
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.
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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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