Cb. Huang et al., PRIMARY BURKITTS-LYMPHOMA OF THE LIVER - REPORT OF A CASE WITH LONG-TERM SURVIVAL AFTER SURGICAL RESECTION AND COMBINATION CHEMOTHERAPY, Journal of pediatric hematology/oncology, 19(2), 1997, pp. 135-138
Purpose: A case of primary Burkitt's cell lymphoma of the liver is rep
orted. Patient: A 14-year-old Chinese boy presented with a 10-day hist
ory of postprandial epigastric pain and weight loss. Results: Preopera
tive imaging studies revealed a large solid mass confined to the right
lobe of the liver; there was no evidence of involvement of other site
s. There was serological and immunohistochemical evidence of asymptoma
tic hepatitis B virus infection. Complete removal of the mass was achi
eved by right hepatic lobectomy. Histological examination revealed a s
mall noncleaved cell lymphoma of Burkitt's type that immunostained pos
itively for B-cell markers. The patient remains well, with no evidence
of disease >8 years after surgical resection and combination chemothe
rapy. Conclusions: Only five cases (two children and three adults) of
primary small noncleaved cell lymphoma of the liver have been reported
. We believe this is the second reported case of childhood hepatic lym
phoma with long-term disease-free survival. Further work is needed to
elucidate the relationship between hepatitis B virus infection and the
development of a primary small noncleaved lymphoma of the liver.