PTLD Classification of 1988 (Nalesnik et al.) | |||||||
---|---|---|---|---|---|---|---|
Category | Lymphocyte Heterogeneity (Polymorphism) | Plasmacytic Cells | Necrosis | Underlying Architecture | Clonality# | Comments | |
Reactive Diffuse Plasma Cell Hyperplasia | Minimal | Marked | No | Intact | Not determined | Described, but relationship to PTLD undefined | |
Polymorphic PTLD | Prominent | Variable | Variable may be prominent | Disrupted* | 17/31 (55%) with Monoclonal component | Includes Polymorphic Hyperplasia and Lymphoma of Frizzera et al. | |
Minimally Polymorphic PTLD | Minimal | Prominent | Variable | Disrupted | 18/22 (82%) with Monoclonal component | Term not widely applied; synonymous with plasmacytoma | |
Monomorphic PTLD | None | Rare to None | Variable | Disrupted | 5/5 (100%) Monoclonal | Synonymous with non-Hodgkin's lymphomas | |
Notes: *Early infiltrative lesions may not have recognizable architectural destruction; #Clonal composition was based on molecular or immunoperoxidase studies in individual cases. |
Reference
|