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Spontaneous bilateral kidney rupture during autologous stem cell transplantation in a patient affected by amyloidosis
Kidney spontaneous rupture is not a recognized complication neither for amyloidosis nor of autologous stem cell transplantation (ASCT). A 46-year-old white woman, affected by nephrotic syndrome, was diagnosed as AL amyloidosis by renal biopsy. We report the singular case of a bilateral spontaneous k...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421635/ https://www.ncbi.nlm.nih.gov/pubmed/25984105 http://dx.doi.org/10.1093/ndtplus/sfq168 |
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author | Ferrannini, Michele Vischini, Gisella De Angelis, Gottardo Giannakakis, Konstantinos Arcese, William |
author_facet | Ferrannini, Michele Vischini, Gisella De Angelis, Gottardo Giannakakis, Konstantinos Arcese, William |
author_sort | Ferrannini, Michele |
collection | PubMed |
description | Kidney spontaneous rupture is not a recognized complication neither for amyloidosis nor of autologous stem cell transplantation (ASCT). A 46-year-old white woman, affected by nephrotic syndrome, was diagnosed as AL amyloidosis by renal biopsy. We report the singular case of a bilateral spontaneous kidney rupture during ASCT for AL with renal rescue. |
format | Online Article Text |
id | pubmed-4421635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44216352015-05-15 Spontaneous bilateral kidney rupture during autologous stem cell transplantation in a patient affected by amyloidosis Ferrannini, Michele Vischini, Gisella De Angelis, Gottardo Giannakakis, Konstantinos Arcese, William NDT Plus Case Report Kidney spontaneous rupture is not a recognized complication neither for amyloidosis nor of autologous stem cell transplantation (ASCT). A 46-year-old white woman, affected by nephrotic syndrome, was diagnosed as AL amyloidosis by renal biopsy. We report the singular case of a bilateral spontaneous kidney rupture during ASCT for AL with renal rescue. Oxford University Press 2011-02 2010-10-05 /pmc/articles/PMC4421635/ /pubmed/25984105 http://dx.doi.org/10.1093/ndtplus/sfq168 Text en © The Author 2010. 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 Ferrannini, Michele Vischini, Gisella De Angelis, Gottardo Giannakakis, Konstantinos Arcese, William Spontaneous bilateral kidney rupture during autologous stem cell transplantation in a patient affected by amyloidosis |
title | Spontaneous bilateral kidney rupture during autologous stem cell transplantation in a patient affected by amyloidosis |
title_full | Spontaneous bilateral kidney rupture during autologous stem cell transplantation in a patient affected by amyloidosis |
title_fullStr | Spontaneous bilateral kidney rupture during autologous stem cell transplantation in a patient affected by amyloidosis |
title_full_unstemmed | Spontaneous bilateral kidney rupture during autologous stem cell transplantation in a patient affected by amyloidosis |
title_short | Spontaneous bilateral kidney rupture during autologous stem cell transplantation in a patient affected by amyloidosis |
title_sort | spontaneous bilateral kidney rupture during autologous stem cell transplantation in a patient affected by amyloidosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421635/ https://www.ncbi.nlm.nih.gov/pubmed/25984105 http://dx.doi.org/10.1093/ndtplus/sfq168 |
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