Polyomavirus-associated nephropathy is an important cause of allo-graft dysfunction and graft loss after kidney transplantation. Even ifhistological evaluation is the gold standard for graft study and diagno-sis of polyomavirus-associated nephropathy, K-DIGO guidelines sug-gest performing an indication biopsyin selected patient’s clinical con-ditions or laboratory parameters. The practice of protocol biopsyis stillcontroversial. We report the management of a case of presumptivepolyomavirus-associated nephropathy in a 53-year-old kidney trans-plant recipient affected by type 1 hyperoxaluria with persistent highlevels of viruria and sustained levels of polyomavirus BK viremia. Thepresence of a presumptive polyomavirus-associated nephropathy, evenif never confirmed by biopsy, never compromised his clinical conditionand allograft function. As a result of an immunosuppression-sparingpolicy and use of mTOR inhibitor, the polyomavirus BK viremia wassuccessfully controlled with an observation time >5 years. The deci-sion to perform or not a graft biopsy was the main question in themanagement of this case. We opted for a non-invasive approachbecause of the high risk of biopsy with macrohematuria on earlierbiopsy in a dual kidney transplant and patient’s unwillingness for theprocedure. The replication level of polyomavirus BK was significantlyreduced by the decrease of immunosuppression on the basis of a closenucleic acid testing monitoring. The strategy we adopted could be con-sidered in cases when renal biopsy is contraindicated or considered tobe high risk

Persistently high-level polyomavirus BK replication in the absence of renal function abnormalities in a kidney transplant recipient

Antonio Curtoni
First
;
Cristina Costa
;
Maria Messina;Francesca Sidoti;Andrea Piceghello;Gabriele Bianco;Luigi Biancone;Giuseppe Paolo Segoloni;Rossana Cavallo
Last
2016-01-01

Abstract

Polyomavirus-associated nephropathy is an important cause of allo-graft dysfunction and graft loss after kidney transplantation. Even ifhistological evaluation is the gold standard for graft study and diagno-sis of polyomavirus-associated nephropathy, K-DIGO guidelines sug-gest performing an indication biopsyin selected patient’s clinical con-ditions or laboratory parameters. The practice of protocol biopsyis stillcontroversial. We report the management of a case of presumptivepolyomavirus-associated nephropathy in a 53-year-old kidney trans-plant recipient affected by type 1 hyperoxaluria with persistent highlevels of viruria and sustained levels of polyomavirus BK viremia. Thepresence of a presumptive polyomavirus-associated nephropathy, evenif never confirmed by biopsy, never compromised his clinical conditionand allograft function. As a result of an immunosuppression-sparingpolicy and use of mTOR inhibitor, the polyomavirus BK viremia wassuccessfully controlled with an observation time >5 years. The deci-sion to perform or not a graft biopsy was the main question in themanagement of this case. We opted for a non-invasive approachbecause of the high risk of biopsy with macrohematuria on earlierbiopsy in a dual kidney transplant and patient’s unwillingness for theprocedure. The replication level of polyomavirus BK was significantlyreduced by the decrease of immunosuppression on the basis of a closenucleic acid testing monitoring. The strategy we adopted could be con-sidered in cases when renal biopsy is contraindicated or considered tobe high risk
2016
31
4
120
122
polyomavirus BK; kidney transplantation; polyomavirus-associated nephropathy; viral replication; real-time PCR
Antonio Curtoni; Cristina Costa; Maria Messina; Francesca Sidoti; Andrea Piceghello; Gabriele Bianco; Luigi Biancone; Giuseppe Paolo Segoloni; Rossana Cavallo
File in questo prodotto:
File Dimensione Formato  
Curtoni et al Microbiologia Medica 2016.pdf

Accesso aperto

Tipo di file: PDF EDITORIALE
Dimensione 602.48 kB
Formato Adobe PDF
602.48 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1901447
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact