Published online Mar 20, 2008.
https://doi.org/10.3802/kjgo.2008.19.1.81
A case of myxoid malignant fibrous histiocytoma in the pelvic cavity
Abstract
Malignant fibrous histiocytoma (MFH) is the most frequent malignant soft tissue tumor in adults. A primary MFH occurs most commonly in the extremities and the trunk, but rarely in the pelvic cavity. We report a case of malignant fibrous histiocytoma of the unknown origin in the pelvic cavity with a review of the literature. The neoplasm occurred in the pelvic cavity of 53-year-old female who complained of enlarging nontender mass in the lower abdomen. The final diagnosis was based on the pathological report of the surgical specimen.
Fig. 1
Abdominal CT scan shows about 10 cm sized heterogeneously enhancing solid mass in pelvic cavity, diffusely attached to anterior wall of uterus and small bowel loops.
Fig. 2
The gross finding of surgically removed retroperitomeal mass: This tumor measuring 12.5X10X6 cm, 400 mg, is gray-white, fresh mass with multifocal hemorrhagic necrosis.
Fig. 3
The tumor cells are arranged with short fascicles consisting of pleomorphic spindle cells (H&E, X200).
Fig. 4
There are pleomorphic spindle cells in myxoid background (H&E, X200).
Fig. 5
On immunohistochemically, tumor cells are positive for vimentin (vimentin, X400).
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