Background. Although 14% of the malignant lymphomas after organ transp
lantation are reported to be T-cell lymphomas, only a few cases are de
scribed in the literature. Methods. The authors presented three new ca
ses. They summarized the clinical data and analyzed histologic and imm
unochemical findings. The presence of Epstein-Barr virus (EBV) and hum
an T-cell lymphoma type 1 (HTLV-1) were investigated. T-cell receptor
(TCR) rearrangement was analyzed by Southern blot technique in two cas
es. Results. Two of the three lymphomas developed after renal transpla
ntation. One was a T-cell lymphoma of pleomorphic medium-sized cell ty
pe and the other was a T-cell lymphoblastic lymphoma; the third T-cell
lymphoma was an anaplastic large cell (Ki-1 positive) type that devel
oped after heart transplantation. No association was established with
EBV or HTLV-1. A monoclonal TCR rearrangement was found in the two cas
es that were analyzed. A literature search revealed 22 other cases. Ni
neteen of the 22 reported cases were peripheral T-cell lymphomas. Almo
st all lymphomas presented in extranodal sites. The time between diagn
osis and organ transplantation seemed to be influenced by the type of
immunosuppressive therapy. In five cases, EBV was detected in the tumo
r cells. A monoclonal T-cell receptor rearrangement was found in eight
cases and a polyclonal proliferation in one case. Response to therapy
was variable, but often poor.Conclusions. The etiology of posttranspl
ant T-cell lymphomas remains unclear, Similarities with posttransplant
B-cell proliferations are the predominant extranodal presentation and
the finding that the time of occurrence is influenced by the type of
immunosuppression. In contrast with posttransplant B-cell proliferatio
ns, only a minority of the cases are associated with EBV. Most tumors
appear to be monoclonal. Prognosis is generally poor, but tumor presen
tation with localized disease might have a somewhat better prognosis.