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A 46-Year-Old Thai Woman with Secondary Acquired Pure Red Cell Aplasia Due to Treatment with Recombinant Erythropoietin While on Dialysis for End-Stage Renal Disease Who Recovered Following ABO-Incompatible Kidney Transplantation

Patient: Female, 46-year-old Final Diagnosis: Pure red cell aplasia (PRCA) undergoing ABO-incompatible kidney transplantation Symptoms: End-stage kidney disease (ESKD) with anemia Medication:— Clinical Procedure: — Specialty: Nephrology OBJECTIVE: Rare disease BACKGROUND: Pure red cell aplasia (PRCA...

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Autores principales: Kitpermkiat, Rungthiwa, Thotsiri, Sansanee, Arpornsujaritkun, Nuttaporn, Sangkum, Premsant, Chantrathammachart, Pichika, Kitpoka, Pimpun, Thammanichanond, Duangtawan, Virankabutra, Tanist, Kantachuvesiri, Surasak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302208/
https://www.ncbi.nlm.nih.gov/pubmed/35842751
http://dx.doi.org/10.12659/AJCR.935451
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author Kitpermkiat, Rungthiwa
Thotsiri, Sansanee
Arpornsujaritkun, Nuttaporn
Sangkum, Premsant
Chantrathammachart, Pichika
Kitpoka, Pimpun
Thammanichanond, Duangtawan
Virankabutra, Tanist
Kantachuvesiri, Surasak
author_facet Kitpermkiat, Rungthiwa
Thotsiri, Sansanee
Arpornsujaritkun, Nuttaporn
Sangkum, Premsant
Chantrathammachart, Pichika
Kitpoka, Pimpun
Thammanichanond, Duangtawan
Virankabutra, Tanist
Kantachuvesiri, Surasak
author_sort Kitpermkiat, Rungthiwa
collection PubMed
description Patient: Female, 46-year-old Final Diagnosis: Pure red cell aplasia (PRCA) undergoing ABO-incompatible kidney transplantation Symptoms: End-stage kidney disease (ESKD) with anemia Medication:— Clinical Procedure: — Specialty: Nephrology OBJECTIVE: Rare disease BACKGROUND: Pure red cell aplasia (PRCA) is an uncommon cause of anemia in end-stage kidney disease (ESKD). It is attributed to recombinant human erythropoietin (rHuEPO) administration. Although immunosuppression is the mainstay therapy, its effectiveness varies from 30% to 70%. PRCA in ESKD has been reported to improve following kidney transplantation. CASE REPORT: A 46-year-old woman with ESKD secondary to lupus nephritis was treated for uremia at our center. She developed severe anemia. Bone marrow aspiration and biopsy revealed a reduction of erythroid precursors, consistent with PRCA. Because she had no sibling’s blood group matched with her, ABO-incompatible kidney transplantation was an option for treatment. She underwent a desensitization protocol consisting of rituximab 375 mg/m(2), tacrolimus, mycophenolate mofetil, and prednisolone 4 weeks before surgery, in addition to 3 sessions of double-filtration plasmapheresis (DFPP) every other day followed by intravenous immunoglobulin (IVIG) and 1 session of specific immunoadsorption (Glycosorb(®) B column) at pre-transplant day −1. She also received low-dose rabbit anti-thymocyte globulin (rATG) (Thymoglobulin(®)) (total 2.0 mg/kg). Maintenance therapy included tacrolimus, mycophenolate mofetil, and prednisolone. Allograft function normalized a few days after transplantation and her Hb gradually increased. CONCLUSIONS: We report a rare case of PRCA in a patient with ESKD undergoing ABO-incompatible kidney transplantation. The outcome was satisfactory, with complete correction of anemia and kidney function.
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spelling pubmed-93022082022-08-01 A 46-Year-Old Thai Woman with Secondary Acquired Pure Red Cell Aplasia Due to Treatment with Recombinant Erythropoietin While on Dialysis for End-Stage Renal Disease Who Recovered Following ABO-Incompatible Kidney Transplantation Kitpermkiat, Rungthiwa Thotsiri, Sansanee Arpornsujaritkun, Nuttaporn Sangkum, Premsant Chantrathammachart, Pichika Kitpoka, Pimpun Thammanichanond, Duangtawan Virankabutra, Tanist Kantachuvesiri, Surasak Am J Case Rep Articles Patient: Female, 46-year-old Final Diagnosis: Pure red cell aplasia (PRCA) undergoing ABO-incompatible kidney transplantation Symptoms: End-stage kidney disease (ESKD) with anemia Medication:— Clinical Procedure: — Specialty: Nephrology OBJECTIVE: Rare disease BACKGROUND: Pure red cell aplasia (PRCA) is an uncommon cause of anemia in end-stage kidney disease (ESKD). It is attributed to recombinant human erythropoietin (rHuEPO) administration. Although immunosuppression is the mainstay therapy, its effectiveness varies from 30% to 70%. PRCA in ESKD has been reported to improve following kidney transplantation. CASE REPORT: A 46-year-old woman with ESKD secondary to lupus nephritis was treated for uremia at our center. She developed severe anemia. Bone marrow aspiration and biopsy revealed a reduction of erythroid precursors, consistent with PRCA. Because she had no sibling’s blood group matched with her, ABO-incompatible kidney transplantation was an option for treatment. She underwent a desensitization protocol consisting of rituximab 375 mg/m(2), tacrolimus, mycophenolate mofetil, and prednisolone 4 weeks before surgery, in addition to 3 sessions of double-filtration plasmapheresis (DFPP) every other day followed by intravenous immunoglobulin (IVIG) and 1 session of specific immunoadsorption (Glycosorb(®) B column) at pre-transplant day −1. She also received low-dose rabbit anti-thymocyte globulin (rATG) (Thymoglobulin(®)) (total 2.0 mg/kg). Maintenance therapy included tacrolimus, mycophenolate mofetil, and prednisolone. Allograft function normalized a few days after transplantation and her Hb gradually increased. CONCLUSIONS: We report a rare case of PRCA in a patient with ESKD undergoing ABO-incompatible kidney transplantation. The outcome was satisfactory, with complete correction of anemia and kidney function. International Scientific Literature, Inc. 2022-07-17 /pmc/articles/PMC9302208/ /pubmed/35842751 http://dx.doi.org/10.12659/AJCR.935451 Text en © Am J Case Rep, 2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Kitpermkiat, Rungthiwa
Thotsiri, Sansanee
Arpornsujaritkun, Nuttaporn
Sangkum, Premsant
Chantrathammachart, Pichika
Kitpoka, Pimpun
Thammanichanond, Duangtawan
Virankabutra, Tanist
Kantachuvesiri, Surasak
A 46-Year-Old Thai Woman with Secondary Acquired Pure Red Cell Aplasia Due to Treatment with Recombinant Erythropoietin While on Dialysis for End-Stage Renal Disease Who Recovered Following ABO-Incompatible Kidney Transplantation
title A 46-Year-Old Thai Woman with Secondary Acquired Pure Red Cell Aplasia Due to Treatment with Recombinant Erythropoietin While on Dialysis for End-Stage Renal Disease Who Recovered Following ABO-Incompatible Kidney Transplantation
title_full A 46-Year-Old Thai Woman with Secondary Acquired Pure Red Cell Aplasia Due to Treatment with Recombinant Erythropoietin While on Dialysis for End-Stage Renal Disease Who Recovered Following ABO-Incompatible Kidney Transplantation
title_fullStr A 46-Year-Old Thai Woman with Secondary Acquired Pure Red Cell Aplasia Due to Treatment with Recombinant Erythropoietin While on Dialysis for End-Stage Renal Disease Who Recovered Following ABO-Incompatible Kidney Transplantation
title_full_unstemmed A 46-Year-Old Thai Woman with Secondary Acquired Pure Red Cell Aplasia Due to Treatment with Recombinant Erythropoietin While on Dialysis for End-Stage Renal Disease Who Recovered Following ABO-Incompatible Kidney Transplantation
title_short A 46-Year-Old Thai Woman with Secondary Acquired Pure Red Cell Aplasia Due to Treatment with Recombinant Erythropoietin While on Dialysis for End-Stage Renal Disease Who Recovered Following ABO-Incompatible Kidney Transplantation
title_sort 46-year-old thai woman with secondary acquired pure red cell aplasia due to treatment with recombinant erythropoietin while on dialysis for end-stage renal disease who recovered following abo-incompatible kidney transplantation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302208/
https://www.ncbi.nlm.nih.gov/pubmed/35842751
http://dx.doi.org/10.12659/AJCR.935451
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