BACKGROUND. Epstein-Barr virus (EBV)-associated myogenic tumors in immunoco
mpromised patients were recently recognized, but their biologic behavior re
mains only partially understood. Although observations so far have permitte
d the recognition of similarities between posttransplant myogenic tumors an
d posttransplant lymphoproliferative disorders (PTLD), the number of report
s are still few, and new experiences continue to be informative.
METHODS. The authors describe what they believe is the first example of pos
ttransplant EBV-associated myogenic tumor involving bone, which is also rem
arkable for its multicentric symmetric limb distribution. Immunohistochemis
try of tumor cells for myogenic antigens (desmin and smooth muscle actin),
EBV antigens (latency proteins latent membrane protein-1 [LMP-1], Epstein-B
arr nuclear antigen-2 [EBNA-2], and ZEBRA), p53, and bcl-2 was examined by
standard avidin-biotin-peroxidase complex methods. Molecular techniques inv
estigated in situ hybridization for Epstein-Barr virus-encoded messenger RN
As (EBERs) and single-strand conformation polymorphism analysis for p53 mut
ation.
RESULTS. Although the biologic behavior of this tumor was uncertain, the re
duction of immunosuppression arrested tumor growth for 5 years, at the expe
nse some loss in renal function. The occurrence of episodes of acute cellul
ar rejection required pulse therapy, resulting in the appearance of new les
ions in both liver and lungs. Despite these complications, a balance betwee
n control of this multicentric tumor growth and allograft survival has been
maintained for 8 years.
CONCLUSIONS. To the authors' knowledge, this example of posttransplant myog
enic tumor is the first described in the bone. It shows partial response to
immunomodulation with persistent tumor, with prolonged survival of the ren
al allograft. (C) 2000 American Cancer Society.