Post-transplantation lymphoproliferative diseases (PTLDs) are a heterogenou
s group of lymphoid proliferative disorders occurring in transplant patient
s. Most PTLDs are B-cell in origin; T-cell PTLDs are seldom reported, and E
BV-associated T-cell PTLDs are rare. The first case of a T-cell, non-EBV-as
sociated PTLD was first described in a renal allograft recipient in 1987. A
total of 40 cases of T-cell PTLDs in solid organ transplant recipients hav
e been reported. However, so far only 16 cases of EBV-associated T-cell PTL
Ds have been reported in the literature. The sites of occurrence of EBV-ass
ociated T-cell PTLDs were in the gastrointestinal tract, lungs, bone marrow
, skin, liver and spleen. The pathogenesis of EBV-associated T-cell PTLD is
uncertain; it is speculated that the EBV may infect a subset of T-cells th
at express the CD21 receptor. The present treatment of EBV-associated T-cel
l PTLD consists of surgical removal, reduction or withdrawal of immunosuppr
ession and/or radiotherapy and chemotherapy. The prognosis is uncertain, an
d the 1-year survival for patients who were followed up for 1 year was 50%.
(C) 2001 Editions scientifiques et medicales Elsevier SAS.