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Collapsing focal segmental glomerulosclerosis following long-term treatment with oral ibandronate: case report and review of literature

BACKGROUND: Renal toxicity has been reported with bisphosphonates such as pamidronate and zolidronate but not with ibandronate, in the treatment of breast cancer patients with bone metastasis. One of the patterns of bisphosphonate-induced nephrotoxicity is focal segmental glomerulosclerosis (FSGS) o...

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Autores principales: Jia, Ning, Cormack, Fionnuala C., Xie, Bin, Shiue, Zita, Najafian, Behzad, Gralow, Julie R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510889/
https://www.ncbi.nlm.nih.gov/pubmed/26197890
http://dx.doi.org/10.1186/s12885-015-1536-y
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author Jia, Ning
Cormack, Fionnuala C.
Xie, Bin
Shiue, Zita
Najafian, Behzad
Gralow, Julie R.
author_facet Jia, Ning
Cormack, Fionnuala C.
Xie, Bin
Shiue, Zita
Najafian, Behzad
Gralow, Julie R.
author_sort Jia, Ning
collection PubMed
description BACKGROUND: Renal toxicity has been reported with bisphosphonates such as pamidronate and zolidronate but not with ibandronate, in the treatment of breast cancer patients with bone metastasis. One of the patterns of bisphosphonate-induced nephrotoxicity is focal segmental glomerulosclerosis (FSGS) or its morphological variant, collapsing focal segmental glomerulosclerosis (CFSGS). CASE PRESENTATION: We describe a breast cancer patient who developed heavy proteinuria (protein/creatinine ratio 9.1) and nephrotic syndrome following treatment with oral ibandronate for 29 months. CFSGS was proven by biopsy. There was no improvement 1 month after ibandronate was discontinued. Prednisone and tacrolimus were started and she experienced a decreased in proteinuria. CONCLUSION: In patient who develops ibandronate-associated CFSGS, proteinuria appears to be at least partially reversible with the treatment of prednisone and/or tacrolimus if the syndrome is recognized early and ibandronate is stopped.
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spelling pubmed-45108892015-07-23 Collapsing focal segmental glomerulosclerosis following long-term treatment with oral ibandronate: case report and review of literature Jia, Ning Cormack, Fionnuala C. Xie, Bin Shiue, Zita Najafian, Behzad Gralow, Julie R. BMC Cancer Case Report BACKGROUND: Renal toxicity has been reported with bisphosphonates such as pamidronate and zolidronate but not with ibandronate, in the treatment of breast cancer patients with bone metastasis. One of the patterns of bisphosphonate-induced nephrotoxicity is focal segmental glomerulosclerosis (FSGS) or its morphological variant, collapsing focal segmental glomerulosclerosis (CFSGS). CASE PRESENTATION: We describe a breast cancer patient who developed heavy proteinuria (protein/creatinine ratio 9.1) and nephrotic syndrome following treatment with oral ibandronate for 29 months. CFSGS was proven by biopsy. There was no improvement 1 month after ibandronate was discontinued. Prednisone and tacrolimus were started and she experienced a decreased in proteinuria. CONCLUSION: In patient who develops ibandronate-associated CFSGS, proteinuria appears to be at least partially reversible with the treatment of prednisone and/or tacrolimus if the syndrome is recognized early and ibandronate is stopped. BioMed Central 2015-07-22 /pmc/articles/PMC4510889/ /pubmed/26197890 http://dx.doi.org/10.1186/s12885-015-1536-y Text en © Jia et al. 2015 This article is published under license to BioMed Central Ltd. 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Jia, Ning
Cormack, Fionnuala C.
Xie, Bin
Shiue, Zita
Najafian, Behzad
Gralow, Julie R.
Collapsing focal segmental glomerulosclerosis following long-term treatment with oral ibandronate: case report and review of literature
title Collapsing focal segmental glomerulosclerosis following long-term treatment with oral ibandronate: case report and review of literature
title_full Collapsing focal segmental glomerulosclerosis following long-term treatment with oral ibandronate: case report and review of literature
title_fullStr Collapsing focal segmental glomerulosclerosis following long-term treatment with oral ibandronate: case report and review of literature
title_full_unstemmed Collapsing focal segmental glomerulosclerosis following long-term treatment with oral ibandronate: case report and review of literature
title_short Collapsing focal segmental glomerulosclerosis following long-term treatment with oral ibandronate: case report and review of literature
title_sort collapsing focal segmental glomerulosclerosis following long-term treatment with oral ibandronate: case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510889/
https://www.ncbi.nlm.nih.gov/pubmed/26197890
http://dx.doi.org/10.1186/s12885-015-1536-y
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