Posttransplant lymphoproliferative disease represents a heterogeneous group of diseases characterized by uncontrolled proliferation of lymphocytes, favored by immunosuppression. Several risk factors for its development have been described, with Epstein-Barr virus infection being a main cause of early-onset forms and chronic antigen stimulation of donors and/or accumulated immunosuppression as key factors of later forms of lymphocyte transformation. The present clinical case presents a patient diagnosed with post transplant lymphoproliferative disease 3 years after renal transplant who had a potentially lethal complication related to conversion to inhibitors of mammalian target of rapamycin. Because clinical studies that establish the most suitable treatment are lacking, it is recommended to identify the strategy, defining possible risks versus benefits of conversion to inhibitors of mammalian target of rapamycin in cases of posttransplant lymphoproliferative disease, and to maintain a high level of surveillance in case of possible secondary effects that can be verified after their introduction.
Key words: Epstein-Barr virus infection, Immunosuppression, Renal transplant
IntroductionPosttransplant lymphoproliferative disease (PTLD) represents a heterogeneous group of diseases characterized by uncontrolled proliferation of lymphocytes, favored by immunosuppression. [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16] Several risk factors for its development have been described, with infection by Epstein-Barr virus being a main cause of early-onset forms and chronic antigen stimulation of donors and/or accumulated immunosuppression as factors of later forms of lymphocyte transformation. 2 In the literature as a first-line treatment after PTLD diagnosis, in addition to specific treatments (chemoradiation, radiotherapy, and/or immunotherapy), it is recommended that either doses of calcineurin inhibitors be decreased or agent converted to inhibitors of mammalian target of rapamycin (imTOR), 10 since, with either, the reduction of immunosuppression would restore the ability of the receptor's immune system to control the uncontrolled proliferation of lymphomatous cells. 3 However, the reduction of immunosuppression is followed by complete remission only in localized and histologically less aggressive forms, with most cases requiring addition of a chemotherapy regimen (rituximab and/or cyclophosphamide, doxorubicin, vincristine, prednisone + rituximab). 4 On the other hand, although an imTOR has an antiproliferative effect, 5 its use is not free from possible secondary effects.Here, we present a patient diagnosed with PTLD 3 years after renal transplant who developed a potentially lethal complication related to conversion to imTOR. Because clinical studies that have established the most suitable treatment are lacking, it is recommended to identify a strategy, defining possible risks versus benefits of the conversion to imTOR in cases of PTLD, and to maintain a high level of surveillance in case of possible s...