Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Gang, Sujin, Park, Sooyong, Min, Sang-il, Hong, Joonshik, Chang, Yoon Hwan, Ha, Jongwon, Yang, Jaeseok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Transplantation 2020
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
_version_ 1784725025093320704
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
work_keys_str_mv AT gangsujin recurrentparvovirusb19infectionassociatedpureredcellaplasiainakidneytransplantpatient
AT parksooyong recurrentparvovirusb19infectionassociatedpureredcellaplasiainakidneytransplantpatient
AT minsangil recurrentparvovirusb19infectionassociatedpureredcellaplasiainakidneytransplantpatient
AT hongjoonshik recurrentparvovirusb19infectionassociatedpureredcellaplasiainakidneytransplantpatient
AT changyoonhwan recurrentparvovirusb19infectionassociatedpureredcellaplasiainakidneytransplantpatient
AT hajongwon recurrentparvovirusb19infectionassociatedpureredcellaplasiainakidneytransplantpatient
AT yangjaeseok recurrentparvovirusb19infectionassociatedpureredcellaplasiainakidneytransplantpatient