Abstract
Posttransplant lymphoproliferative disorders (PTLDs) are lymphoid or plasmacytic proliferations that develop in solid organ, bone marrow, or stem cell allograft recipients in a setting of immunosuppression. PTLDs’ spectrum ranges from usually EBV-driven reactive lymphoid/plasmacytic proliferations to EBV+ or EBV− monoclonal lymphomas or plasmacytic neoplasms, as well as classical Hodgkin lymphoma, indistinguishable from true B-cell/plasma cell or less often T/NK-cell lymphomas occurring in immunocompetent individuals. There are four major categories of PTLD: nondestructive, polymorphic (P-PTLD), monomorphic (M-PTLD), and classical Hodgkin lymphoma (HL-PTLD) PTLDs. Nondestructive PTLDs, including plasmacytic hyperplasia, infectious mononucleosis, and florid follicular hyperplasia, are characterized by some degree of architecture preservation of the involved tissue, with preservation of the nodal sinuses or tonsillar crypts, and residual or florid reactive follicles (FFH) in some cases but an absence of any diagnostic features of a malignant lymphoma of the latter three categories or other known explanations and nonspecific chronic inflammatory processes.
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Wang, J. (2020). Posttransplant Lymphoproliferative Disorders (PTLDs). In: Wang, E., Lagoo, A.S. (eds) Practical Lymph Node and Bone Marrow Pathology. Practical Anatomic Pathology. Springer, Cham. https://doi.org/10.1007/978-3-030-32189-5_10
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DOI: https://doi.org/10.1007/978-3-030-32189-5_10
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