scholarly journals COVID-19–Associated Graft Loss From Renal Infarction in a Kidney Transplant Recipient

2021 ◽  
Vol 6 (4) ◽  
pp. 1166-1169
Author(s):  
Christine Webb ◽  
Bianca Davidson ◽  
Erika S.W. Jones ◽  
Nicola Wearne ◽  
Dharshnee Rama Chetty ◽  
...  
2020 ◽  
Vol 31 (4) ◽  
pp. 387-391 ◽  
Author(s):  
Gaetano Alfano ◽  
Francesco Fontana ◽  
Giovanni Guaraldi ◽  
Gianni Cappelli ◽  
Cristina Mussini

BK virus (BKV) is an opportunistic pathogen in those with impaired immunity. Viral replication is generally asymptomatic but is able to induce cytopathic alterations in renal cells. If BKV infection is left untreated, it leads to BKV-associated nephropathy (BKVAN) and graft loss. There is scarce experience in the management of BKV infection in kidney transplant recipients living with HIV. We report the successful treatment of BKVAN in an HIV-positive kidney transplant recipient who experienced BKV replication in the immediate post-transplantation period. A change in therapy from calcineurin inhibitor to sirolimus, steroid withdrawal and a short course of an immunomodulatory agent (leflunomide) controlled BKV viremia in the absence of drug side-effects or impairment of graft function.


2016 ◽  
Vol 31 (4) ◽  
Author(s):  
Antonio Curtoni ◽  
Cristina Costa ◽  
Maria Messina ◽  
Francesca Sidoti ◽  
Andrea Piceghello ◽  
...  

Polyomavirus-associated nephropathy is an important cause of allograft dysfunction and graft loss after kidney transplantation. Even if histological evaluation is the gold standard for graft study and diagnosis of polyomavirus-associated nephropathy, K-DIGO guidelines suggest performing an <em>indication biopsy</em> in selected patient’s clinical conditions or laboratory parameters. The practice of <em>protocol biopsy</em> is still controversial. We report the management of a case of presumptive polyomavirus-associated nephropathy in a 53-year-old kidney transplant recipient affected by type 1 hyperoxaluria with persistent high levels of viruria and sustained levels of polyomavirus BK viremia. The presence of a presumptive polyomavirus-associated nephropathy, even if never confirmed by biopsy, never compromised his clinical condition and allograft function. As a result of an immunosuppression-sparing policy and use of mTOR inhibitor, the polyomavirus BK viremia was successfully controlled with an observation time &gt;5 years. The decision to perform or not a graft biopsy was the main question in the management of this case. We opted for a non-invasive approach because of the high risk of biopsy with macrohematuria on earlier biopsy in a dual kidney transplant and patient’s unwillingness for the procedure. The replication level of polyomavirus BK was significantly reduced by the decrease of immunosuppression on the basis of a close nucleic acid testing monitoring. The strategy we adopted could be considered in cases when renal biopsy is contraindicated or considered to be high risk.


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