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Recurrent parvovirus B19 infection-associated pure red cell aplasia in a kidney transplant patient
Posttransplant anemia is a common complication after kidney transplantation. Parvovirus B19 (PVB19) infection can induce pure red cell aplasia (PRCA) in immunosuppressed transplant patients. We herein report a case of recurrent PVB19-associated PRCA in a kidney transplant patient. A 49-year-old woma...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Transplantation
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9186813/ https://www.ncbi.nlm.nih.gov/pubmed/35769066 http://dx.doi.org/10.4285/kjt.2020.34.3.199 |
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author | Gang, Sujin Park, Sooyong Min, Sang-il Hong, Joonshik Chang, Yoon Hwan Ha, Jongwon Yang, Jaeseok |
author_facet | Gang, Sujin Park, Sooyong Min, Sang-il Hong, Joonshik Chang, Yoon Hwan Ha, Jongwon Yang, Jaeseok |
author_sort | Gang, Sujin |
collection | PubMed |
description | Posttransplant anemia is a common complication after kidney transplantation. Parvovirus B19 (PVB19) infection can induce pure red cell aplasia (PRCA) in immunosuppressed transplant patients. We herein report a case of recurrent PVB19-associated PRCA in a kidney transplant patient. A 49-year-old woman presented with anemia and normal renal function 1 year after a deceased-donor kidney transplantation for immunoglobulin A nephropathy-related end-stage renal disease. She received desensitization therapy, and 2 years later, she underwent transplantation with thymoglobulin induction. Despite repeated red cell transfusion and erythropoietin therapy, her anemia aggravated progressively. Bone marrow biopsy revealed normocytic normochromic PRCA. Real-time polymerase chain reaction detected a high plasma load of PVB19. Administration of intravenous immunoglobulin (IVIG) at 2 g/kg with adjuvant reduction of tacrolimus and discontinuation of myfortic acid effectively treated the anemia. However, the PVB19 load remained high, and PRCA recurred 7 months after the initial IVIG treatment. Tacrolimus was switched to cyclosporine in the second IVIG treatment, which successfully improved PRCA and reduced the PVB19 load. Our case suggested that PVB19-associated PRCA should be suspected when persistent anemia is observed in kidney transplant patients with heavy immunosuppression and that PVB19-associated PRCA can recur in the presence of persistent PVB19 viremia. |
format | Online Article Text |
id | pubmed-9186813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Society for Transplantation |
record_format | MEDLINE/PubMed |
spelling | pubmed-91868132022-06-28 Recurrent parvovirus B19 infection-associated pure red cell aplasia in a kidney transplant patient Gang, Sujin Park, Sooyong Min, Sang-il Hong, Joonshik Chang, Yoon Hwan Ha, Jongwon Yang, Jaeseok Korean J Transplant Case Report Posttransplant anemia is a common complication after kidney transplantation. Parvovirus B19 (PVB19) infection can induce pure red cell aplasia (PRCA) in immunosuppressed transplant patients. We herein report a case of recurrent PVB19-associated PRCA in a kidney transplant patient. A 49-year-old woman presented with anemia and normal renal function 1 year after a deceased-donor kidney transplantation for immunoglobulin A nephropathy-related end-stage renal disease. She received desensitization therapy, and 2 years later, she underwent transplantation with thymoglobulin induction. Despite repeated red cell transfusion and erythropoietin therapy, her anemia aggravated progressively. Bone marrow biopsy revealed normocytic normochromic PRCA. Real-time polymerase chain reaction detected a high plasma load of PVB19. Administration of intravenous immunoglobulin (IVIG) at 2 g/kg with adjuvant reduction of tacrolimus and discontinuation of myfortic acid effectively treated the anemia. However, the PVB19 load remained high, and PRCA recurred 7 months after the initial IVIG treatment. Tacrolimus was switched to cyclosporine in the second IVIG treatment, which successfully improved PRCA and reduced the PVB19 load. Our case suggested that PVB19-associated PRCA should be suspected when persistent anemia is observed in kidney transplant patients with heavy immunosuppression and that PVB19-associated PRCA can recur in the presence of persistent PVB19 viremia. The Korean Society for Transplantation 2020-09-30 2020-09-30 /pmc/articles/PMC9186813/ /pubmed/35769066 http://dx.doi.org/10.4285/kjt.2020.34.3.199 Text en Copyright © 2020 The Korean Society for Transplantation https://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 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Gang, Sujin Park, Sooyong Min, Sang-il Hong, Joonshik Chang, Yoon Hwan Ha, Jongwon Yang, Jaeseok Recurrent parvovirus B19 infection-associated pure red cell aplasia in a kidney transplant patient |
title | Recurrent parvovirus B19 infection-associated pure red cell aplasia in a kidney transplant patient |
title_full | Recurrent parvovirus B19 infection-associated pure red cell aplasia in a kidney transplant patient |
title_fullStr | Recurrent parvovirus B19 infection-associated pure red cell aplasia in a kidney transplant patient |
title_full_unstemmed | Recurrent parvovirus B19 infection-associated pure red cell aplasia in a kidney transplant patient |
title_short | Recurrent parvovirus B19 infection-associated pure red cell aplasia in a kidney transplant patient |
title_sort | recurrent parvovirus b19 infection-associated pure red cell aplasia in a kidney transplant patient |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9186813/ https://www.ncbi.nlm.nih.gov/pubmed/35769066 http://dx.doi.org/10.4285/kjt.2020.34.3.199 |
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