BACKGROUND: Myxoid leiomyosarcoma is a rare variant of uterine sarcoma, exh
ibiting malignant biologic behavior despite the absence of cytologic atypia
and of significant mitotic activity.
CASE: A 20-year-old-female was referred with a cystic pelvic mass. At lapar
otomy, the tumor, weighed 2,200 g and originating in the left lateral uteri
ne wall, was removed. Microscopic examination revealed well-differentiated
smooth muscle cells without atypia and with a fe so mitotic figures in the
copious myxoid matrix, suggesting myxoid leiomyosarcoma. Three years follow
ing laparotomy, an irregular mass around the uterus teas noted on sonograph
ic examination, suggesting local recurrence. Two years and six months later
, the second operation was performed, and a locally recurrent, multicystic
tumor weighing 3,500 g was excised. The histopathology was similar to that
of the primary tumor. Cytologic findings on imprint material from the tumor
revealed a few isolated or sheet like small cells consisting of spindle an
d polygonal cells with round and oval nuclei. Cytologic atypia was also min
imal.
CONCLUSION: 12 Myxoid leiomyosarcoma should be included in the differential
diagnosis of smooth muscle neoplasia.