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[Isolated mesenteric fibromatosis. A clinical case].
G De Toma1, M Plocco, V Nicolanti
1I Cattedra di Clinica Chirurgica, Università degli Studi La Sapienza, Roma.
Il Giornale Di Chirurgia
|June 25, 1999
Summary
This case study discusses isolated mesenteric fibromatosis, a rare benign tumor. Complete surgical removal is the recommended treatment due to frequent local recurrences and lack of effective alternative therapies.
Area of Science:
- Gastroenterology
- Surgical Oncology
Background:
- Mesenteric fibromatosis (MF) is a rare benign neoplasm originating from connective tissue in the mesentery.
- It is often associated with familial adenomatous polyposis (FAP) or Gardner's syndrome, but can occur in isolation.
Observation:
- The case presented is an isolated mesenteric fibromatosis, unassociated with FAP, Gardner's syndrome, or prior abdominal surgery.
- The neoplasm was asymptomatic until it caused symptoms due to compression of the bowel or ureter.
Findings:
- Mesenteric fibromatosis, despite being benign, frequently recurs locally after surgical excision.
- Current therapeutic modalities beyond surgery have yielded unsatisfactory results.
Implications:
- This case highlights the importance of considering isolated mesenteric fibromatosis in the differential diagnosis of abdominal masses.
- Effective management strategies for mesenteric fibromatosis require further investigation to improve outcomes and reduce recurrence rates.