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Rituximab: A viable treatment option for epoetin-induced pure red cell aplasia

Pure red cell aplasia (PRCA) due to neutralizing antibodies can rarely develop following treatment with epoetin. The treatment of this condition is generally unsatisfactory and immunosuppression is often recommended, which improves chances of hematological recovery. We describe a case of PRCA due to...

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Detalles Bibliográficos
Autores principales: Mahajan, S. A., Nandagopal, N., Soni, M., Annigeri, R. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4663775/
https://www.ncbi.nlm.nih.gov/pubmed/26664213
http://dx.doi.org/10.4103/0971-4065.156897
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author Mahajan, S. A.
Nandagopal, N.
Soni, M.
Annigeri, R. A.
author_facet Mahajan, S. A.
Nandagopal, N.
Soni, M.
Annigeri, R. A.
author_sort Mahajan, S. A.
collection PubMed
description Pure red cell aplasia (PRCA) due to neutralizing antibodies can rarely develop following treatment with epoetin. The treatment of this condition is generally unsatisfactory and immunosuppression is often recommended, which improves chances of hematological recovery. We describe a case of PRCA due to neutralizing anti-epoetin antibodies following therapy with epoetin-α in a 68-year-old man on hemodialysis. He presented with severe transfusion-dependent anemia and was initially treated with prednisolone and oral cyclophosphamide. However, within 2 weeks the immunosuppressive drugs had to be stopped due to complications, following which he remained transfusion dependent. Subsequently, he was given two doses 700 mg each of rituximab following which there were hematological recovery and resolution of anti-epoetin antibodies.
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spelling pubmed-46637752015-12-10 Rituximab: A viable treatment option for epoetin-induced pure red cell aplasia Mahajan, S. A. Nandagopal, N. Soni, M. Annigeri, R. A. Indian J Nephrol Case Report Pure red cell aplasia (PRCA) due to neutralizing antibodies can rarely develop following treatment with epoetin. The treatment of this condition is generally unsatisfactory and immunosuppression is often recommended, which improves chances of hematological recovery. We describe a case of PRCA due to neutralizing anti-epoetin antibodies following therapy with epoetin-α in a 68-year-old man on hemodialysis. He presented with severe transfusion-dependent anemia and was initially treated with prednisolone and oral cyclophosphamide. However, within 2 weeks the immunosuppressive drugs had to be stopped due to complications, following which he remained transfusion dependent. Subsequently, he was given two doses 700 mg each of rituximab following which there were hematological recovery and resolution of anti-epoetin antibodies. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4663775/ /pubmed/26664213 http://dx.doi.org/10.4103/0971-4065.156897 Text en Copyright: © Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Mahajan, S. A.
Nandagopal, N.
Soni, M.
Annigeri, R. A.
Rituximab: A viable treatment option for epoetin-induced pure red cell aplasia
title Rituximab: A viable treatment option for epoetin-induced pure red cell aplasia
title_full Rituximab: A viable treatment option for epoetin-induced pure red cell aplasia
title_fullStr Rituximab: A viable treatment option for epoetin-induced pure red cell aplasia
title_full_unstemmed Rituximab: A viable treatment option for epoetin-induced pure red cell aplasia
title_short Rituximab: A viable treatment option for epoetin-induced pure red cell aplasia
title_sort rituximab: a viable treatment option for epoetin-induced pure red cell aplasia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4663775/
https://www.ncbi.nlm.nih.gov/pubmed/26664213
http://dx.doi.org/10.4103/0971-4065.156897
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