Abstract
Post-transplant lymphoproliferative disorders (PTLDs) comprise a wide spectrum of lymphoproliferative disorders that may be difficult to classify. They are potentially lethal, but clinical behavior is not always predictable from the histologic appearance. Factors that contribute to the development of PTLD include the type of transplant (solid organ versus bone marrow), degree of immunosuppression (which in turn generally relates to the type and duration of immunosuppressive therapy), HLA type, and viral status of the individual patient at the time of transplantation. Although the majority of cases of PTLDs are related to infection with the Epstein-Barr virus (EBV), there remains a subset of EBV-negative lymphomas that are less well-characterized. The spectrum of B-cell and N/K T-cell proliferations is illustrated from aggressive lymphomas to indolent localized EBV-related mucocutaneous ulcers.
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Said, J. (2016). Post-transplantation Lymphoproliferative Disorders. In: Wallace, W., Naini, B. (eds) Practical Atlas of Transplant Pathology. Springer, Cham. https://doi.org/10.1007/978-3-319-23054-2_9
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DOI: https://doi.org/10.1007/978-3-319-23054-2_9
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