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Malignancy following organ transplantation is an increasingly important issue facing transplant clinicians, particularly as recipients survive longer (1,2). Among the more interesting of these malignancies are the post-transplant lymphoproliferative diseases (PTLD) because of the spectrum of diseases that occur, sometimes soon after transplantation and in other cases years post-transplant, and their unique relationship to the Epstein-Barr virus (EBV) (3). Studies have shown that there are four primary types of disease, the classification of which have important therapeutic and prognostic implications, and include: uncomplicated infectious mononucleosis; benign polyclonal B-cell hyperplasia without evidence of malignant transformation as shown by the absence of cytogenetic abnormalities or immunoglobulin gene rearrangements; the intermediate polymorphic B-cell lymphoma that is predominantly a polyclonal B-cell proliferation, but contains a subpopulation of malignantly transformed cells with clonal cytogenetic abnormalities and immunoglobulin gene rearrangements; and malignant monoclonal or oligoclonal B-cell lymphoma with clonal cytogenetic abnormalities and immunoglobulin gene rearrangements in a majority of cells (4).
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Douglas W. Hanto (2004) studied this question.
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