Abstract
Immunosuppressed organ transplant recipients have an increased risk of developing cancer such as Kaposi’s sarcoma and posttransplant lymphoproliferative disorders (PTLDs) [1–3]. After organ transplantation, about 40% of patients with PTLDs survive, either because of spontaneous resolution after the cessation of immunosuppressive therapy, or possibly because of the efficacy of antiviral drugs, monoclonal antibodies and chemoradiotherapy [4]. Determination of the best treatment is difficult because of the limited number of published series, and because of the morphologic spectrum of the lymphoproliferative disorders which appears to range from a benign reactive lymphoid process to a malignant lymphoma. We reexamined our experience of 28 transplant recipients with a PTLD observed at our institution in an attempt to determine the response to therapy in 25 treated patients with reduction of immunosuppressants, monoclonal antibodies, surgery and/or chemotherapy after a median of follow-up of 60 months (range 4–84 months).
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Leblond, V. et al. (1996). Therapeutic issues in lymphoproliferative disorders: Treatment and outcome of 28 cases observed in a single center. In: Touraine, J.L., Traeger, J., Bétuel, H., Dubernard, J.M., Revillard, J.P., Dupuy, C. (eds) Cancer in Transplantation: Prevention and Treatment. Transplantation and Clinical Immunology, vol 27. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-0175-9_30
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DOI: https://doi.org/10.1007/978-94-009-0175-9_30
Publisher Name: Springer, Dordrecht
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