Cw. Ross et al., GAMMA DELTA T-CELL POSTTRANSPLANTATION LYMPHOPROLIFERATIVE DISORDER PRIMARILY IN THE SPLEEN/, American journal of clinical pathology, 102(3), 1994, pp. 310-315
A 31-year-old renal transplant recipient developed an unusual T-cell l
ymphoproliferative disorder 3 years after transplantation. The neoplas
m involved the spleen, without concomitant hepatomegaly, lymphadenopat
hy, or obvious bone marrow involvement. Peripheral blood involvement d
eveloped after splenectomy. Immunophenotypically, the neoplastic cells
expressed CD2, CD3, CD7, CD16, CD45, CD56, and the gamma/delta T-cell
receptor on the surface membrane. The neoplastic cells were negative
for surface membrane CD4, CD5, and CD8. Serologic and/or DNA analyses
for viruses, including Epstein-Barr virus, human T-cell lymphotropic v
irus-1, human immunodeficiency virus, and human herpesvirus-6, were ne
gative. Cytogenetic findings included a translocation breakpoint at ch
romosome 7p15, consistent with involvement of the T-cell receptor gamm
a-chain locus. Although gamma/delta T-cell lymphomas have been reporte
d to have a predilection for hepatosplenic localization, this is the f
irst,fell-documented case to be described in the setting of posttransp
lantation immunosuppression.