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ePublished: 30 Nov 2015
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J Renal Inj Prev. 2015;4(4): 135-138.
doi: 10.12861/jrip.2015.28
PMID: 26693501
PMCID: PMC4685984
  Abstract View: 3989
  PDF Download: 1869

Case Report

De novo post-transplant thrombotic microangiopathy localized only to the graft in autosomal dominant polycystic kidney disease with thrombophilia

Davide Rolla 1*, Iris Fontana 2, Jean Louis Ravetti 3, Luigina Marsano 4, Diego Bellino 4, Laura Panaro 4, Francesca Ansaldo 4, Lisa Mathiasen 5, Giulia Storace 1, Matteo Trezzi 1

1 Divisione di Nefrologia – Dialisi –Trapianto, Ospedale Sant’Andrea, La Spezia, Italy
2 Divisione di Chirurgia Vascolare e Trapianto di rene, Azienda Ospedaliera Universitaria San Martino, Genova, Italy
3 Servizio di Anatomia Patologica, Azienda Ospedaliera Universitaria San Martino, Genova, Italy
4 Clinica Nefrologica, Azienda Ospedaliera Universitaria San Martino, Genova, Italy
5 Estor Spa, Pero, Milan, Italy
*Corresponding Author: *Corresponding author: Davide Rolla, , Email: davide.rolla@asl5.liguria.it

Abstract

Introduction: Thrombotic microangiopathy (TMA) is a serious complication of renal transplantation and is mostly related to the prothrombotic effect of calcineurin inhibitors (CNIs). A subset of TMA (29%-38%) is localized only to the graft.

Case 1: A young woman suffering from autosomal dominant polycystic kidney disease (ADPKD) underwent kidney transplant. After 2 months, she showed slow renal deterioration (serum creatinine from 1.9 to 3.1 mg/dl), without hematological signs of hemolytic-uremic syndrome (HUS); only LDH enzyme transient increase was detected. Renal biopsy showed TMA: temporary withdraw of tacrolimus and plasmapheresis was performed. The renal function recovered (serum creatinine 1.9 mg/dl). From screening for thrombophilia, we found a mutation of the Leiden factor V gene.

Case 2: A man affected by ADPKD underwent kidney transplantation, with delay graft function; first biopsy showed acute tubular necrosis, but a second biopsy revealed TMA, while no altered hematological parameters of HUS was detected. We observed only a slight increase of lactate dehydrogenase (LDH) levels. The tacrolimus was halved and plasmapheresis was performed: LDH levels normalized within 10 days and renal function improved (serum creatinine from 9 to 2.9 mg/dl). We found a mutation of the prothrombin gene. Only a renal biopsy clarifies the diagnosis of TMA, but it is necessary to pay attention to light increasing level of LDH.

Conclusion: Prothrombotic effect of CNIs and mTOR inhibitor, mutation of genes encoding factor H or I, anticardiolipin antibodies, vascular rejection, cytomegalovirus infection are proposed to trigger TMA; we detected mutations of factor II and Leiden factor V, as facilitating conditions for TMA in patients affected by ADPKD.


Implication for health policy/practice/research/medical education:

Thrombotic microangiopathy (TMA) is a serious complication of renal transplantation and is mostly related to the prothrombotic effect of calcineurin inhibitors (CNIs). A subset of TMA (29%-38%) is localized only to the graft. Anomalies of coagulation can be permissive for the development of TMA.

Please cite this paper as: Rolla D, Fontana I, Ravetti JL, Marsano L, Bellino D, Panaro L, et al. De novo post-transplant thrombotic microangiopathy localized only to the graft in autosomal dominant polycystic kidney disease with thrombophilia. J Renal Inj Prev. 2015;4(4):135-138. DOI: 10.12861/jrip.2015.28

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