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Long-term survival after post-transplant lymphoproliferative disease in children
Sylvie Nathanson1, Dominigue Debray, Arnaud Delarue
1Service de Néphrologie Pédiatrique, Hôpital Armand-Trousseau, 26 Avenue Arnold-Netter, 75571 Paris cedex 12, France.
Abstract:
Post-transplant lymphoproliferative disease (PTLD) is a well-known complication of immunosuppressive therapy. We present a series of 19 children who developed PTLD, following renal transplantation in 11 and liver transplantation in 8. The mean time between transplantation and the onset of PTLD was 19.5 months. Two patients had T-cell PTLD and died despite intensive chemotherapy. B-cell PTLD was observed in 17 patients and was associated with proven Epstein-Barr virus infection in 9. Despite immediate reduction of immunosuppressive therapy, only 8 of these 17 patients were alive at a 5.6-year mean follow-up. None of these patients had recurrence of PTLD when immunosuppression was resumed.