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Well-differentiated mesenteric liposarcoma: report of two cases
Gaetano Poillucci1, Mauro Podda2, Adolfo Pisanu3
1Department of General Surgery, San Giovanni Addolorata Hospital, Rome, Italy.. gaetano.poillucci@gmail.com.
Acta Bio-Medica : Atenei Parmensis
|March 9, 2022
Summary
We present two rare cases of primary mesenteric liposarcoma, a challenging cancer. Both patients with liposarcoma underwent successful surgical tumor resection, highlighting surgery as a viable treatment option.
Area of Science:
- Oncology
- Surgical Oncology
- Gastrointestinal Oncology
Background:
- Liposarcoma is a rare malignancy with challenging diagnosis and treatment due to nonspecific symptoms and lack of established therapies.
- Surgical resection is the primary treatment for localized liposarcoma, but management can be complex.
- Primary mesenteric liposarcoma is exceptionally rare, posing unique clinical and surgical challenges.
Observation:
- This report details two distinct cases of primary mesenteric liposarcoma.
- The first case presented with significant symptoms of small bowel obstruction, including abdominal distention and severe pain.
- The second case was an incidental finding during surgery for an incisional hernia.
Findings:
- Histopathological examination confirmed well-differentiated liposarcoma in both patients.
- Both patients successfully underwent complete surgical resection of the mesenteric tumors.
- The diverse clinical presentations underscore the varied manifestations of mesenteric liposarcoma.
Implications:
- These cases demonstrate that surgical resection is a feasible and effective treatment for primary mesenteric liposarcoma.
- Early diagnosis and prompt surgical intervention are crucial for favorable outcomes in liposarcoma management.
- Further research into the optimal diagnostic and therapeutic strategies for rare liposarcomas is warranted.

