BackgroundPTLD is a rare heterogenous group of lymphoproliferative diseases arising from chronic immunosuppression after solid organ or allogeneic stem cell transplantation (allo-SCT).Treatment of PTLD involves a sequential approach with immunosuppression reduction and chemoimmunotherapy.
No takes yet. Share an insight, caveat, or question.
Togni et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: