Key result
Surgical resection successfully treated a rare case of multiple primary mesenteric liposarcomas arising from the transverse mesocolon in a 63-year-old female.
Case Report (n=1)
No
Primary mesenteric liposarcoma of the transverse mesocolon is a rare entity that can be successfully treated with surgical resection with clear margins.
Resection may benefit rare mesenteric liposarcomas; leaves open optimal margins, recurrence risk, and need for prospective data.
Liposarcomas are common tumors arising in the retroperitoneum. However, a primary mesenteric liposarcoma is a rare entity and less than 50 cases have been reported so far. Further, a liposarcoma arising in the transverse mesocolon is very unusual, and cases of multiple primary tumors arising from the transverse mesocolon are extremely rare. We want to report a case of a multiple primary mesenteric liposarcoma arising from the transverse mesocolon in a 63-year-old female who was successfully treated by surgery. Because a primary mesenteric liposarcoma is a rare entity, it should be considered with the differential diagnosis of an abdominal mesenchymal tumor. It can be diagnosed preoperatively by using contrast enhanced computed tomography and magnetic resonance imaging. The treatment for such a liposarcoma is surgical resection with sufficient surgical margin; the role of adjuvant therapy has yet to be defined.
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Sachidananda et al. (2013) conducted a case report in Primary Multiple Mesenteric Liposarcoma of the Transverse Mesocolon (n=1). Surgical resection was evaluated. Surgical resection successfully treated a rare case of multiple primary mesenteric liposarcomas arising from the transverse mesocolon in a 63-year-old female.
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