Background: Mesoblastic nephroma is an uncommon renal tumor of infancy and
rarely occurs in adults. We report an adult case of mesoblastic nephroma.
Methods: A 50-year-old woman was found incidentally to have a right renal m
ass by abdominal ultrasonography. Computed tomography and magnetic resonanc
e imaging revealed a heterogeneous tumor and angiography showed a mixture o
f hypervascularity and hypovascularity. Right radical nephrectomy was perfo
rmed.
Results:. The tumor was an encapsulated yellowish solid mass. Microscopical
ly, the tumor was composed of spindle cell proliferation. Atypia and mitose
s were not identified. Among the tumor cells, there were tubular arranged e
pithelial elements.
Conclusion: The patient was free of recurrence 14 months postoperatively. M
esoblastic nephroma is classified as a benign tumor but recurrence and mali
gnant formation of this tumor have been reported so regular postoperative f
ollow up is required.