Mast cell sarcoma is a rare disease. We report an unusual case of this neop
lasm arising in the ascending colon of a 32-year-old Japanese woman who pre
sented with abdominal pain. An ulcerating mass in the colon was resected, a
long with enlarged mesenteric lymph nodes. Two years after surgery, the neo
plasm recurred as left cervical lymphadenopathy and an intra-abdominal mass
, Despite predonine and radiation therapy, the disease progressed, and the
patient died. The tumor cells had abundant fine granular or clear cytoplasm
, and oval, lobulated, or indented nuclei, Numerous mature eosinophils were
intermingled with the tumor cells. Immunohistologic studies on paraffin se
ctions demonstrated that the majority of the tumor cells were strongly posi
tive for CD45RB, CD68, and mast cell tryptase. They were unreactive, howeve
r, with a broad spectrum of antibodies against myelomonocytic and lymphocyt
ic antigens. The mast cell nature of this rare type of tumor can be best id
entifiable by immunostains for mast cell tryptase.