Rp. Ghorbani et al., INTRAGRAFT ANGIOTROPIC LARGE-CELL LYMPHOMA OF T-CELL-TYPE IN A LONG-TERM RENAL-ALLOGRAFT RECIPIENT, Modern pathology, 9(6), 1996, pp. 671-676
Chronic immune suppression is a risk for the development of post-trans
plantation lymphoproliferative disorders, which are frequently caused
by a B-cell dyscrasia We report a unique primary presentation of the r
are angiotropic lymphoma in a kidney allograft, 18 years after transpl
antation. The diagnosis was made by a percutaneous allograft biopsy sp
ecimen when the recipient presented with renal dysfunction and intermi
ttent hematuria Immunostaining of the biopsy specimen revealed a T-cel
l lineage of the neoplastic cells rather than the more common B-cell s
ource. At the time of biopsy, there was no evidence of systemic dissem
ination of lymphoma The intragraft lymphoma resolved completely after
chemotherapy, but the patient died 6 months later as a result of an in
tracerebral hemorrhage. At autopsy, intravascular lymphoma was only fo
und in the cerebral vessels. To the authors' knowledge, this is the fi
rst report of angiotropic T-cell lymphoma in a kidney allograft. A des
cription of the clinical, pathologic, and immunohistochemical features
of this case is provided, as well as reviews of previous reports of r
enal angiotropic lymphoma and post-transplantation T-cell lymphomas.