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Haematological disorders following kidney transplantation.

Authors :
Malyszko J
Basak G
Batko K
Capasso G
Capasso A
Drozd-Sokolowska J
Krzanowska K
Kulicki P
Matuszkiewicz-Rowinska J
Soler MJ
Sprangers B
Malyszko J
Source :
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association [Nephrol Dial Transplant] 2022 Feb 25; Vol. 37 (3), pp. 409-420.
Publication Year :
2022

Abstract

Transplantation offers cure for some haematological cancers, end-stage organ failure, but at the cost of long-term complications. Renal transplantation is the best-known kidney replacement therapy and it can prolong end-stage renal disease patient lives for decades. However, patients after renal transplantation are at a higher risk of developing different complications connected not only with surgical procedure but also with immunosuppressive treatment, chronic kidney disease progression and rejection processes. Various blood disorders can develop in post-transplant patients ranging from relatively benign anaemia through cytopenias to therapy-related myelodysplasia and acute myeloid leukaemia (AML) and post-transplant lymphoproliferative disorders followed by a rare and fatal condition of thrombotic microangiopathy and haemophagocytic syndrome. So far literature mainly focused on the post-transplant lymphoproliferative disease. In this review, a variety of haematological problems after transplantation ranging from rare disorders such as myelodysplasia and AML to relatively common conditions such as anaemia and iron deficiency are presented with up-to-date diagnosis and management.<br /> (© The Author(s) 2020. Published by Oxford University Press on behalf of the ERA.)

Details

Language :
English
ISSN :
1460-2385
Volume :
37
Issue :
3
Database :
MEDLINE
Journal :
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Publication Type :
Academic Journal
Accession number :
33150431
Full Text :
https://doi.org/10.1093/ndt/gfaa219