PTLD - #addtoyournotes
PTLD complicates solid organ or bone marrow transplantation in 1% to 10% of cases. B-cell proliferations account for 95% of cases; the others are T-cell lymphomas. PTLD encompasses at least three clinicopathologic forms: Plasmacytic hyperplasia or infectious mononucleosis-like PTLD occurs in children and young adults early after transplantation, involving lymph nodes and tonsils. It resolves with reduction in immunosuppression.Polymorphic PTLD is more aggressive and consists of clonal growth of a mixed, pleomorphic population of lymphocytes, immunoblasts, and plasma cells that efface lymph node architecture.Monomorphic PTLD is a lymphoma, usually with the features of diffuse large B-cell lymphoma EBV is detected in 80% to 85% of all PTLD cases.PTLD is being increasingly recognised in these days with more transplant recipients - Get up to date changes in medicine. Added to Revision Series - Subscribe here today