A Rare Case of Recurrent Intra-abdominal Desmoid-Type Fibromatosis
Desmoid-type fibromatosis is an uncommon fibroblastic or myofibroblastic tumour arising in deep soft tissues with no metastatic potential. This case report presents a 78-year-old male patient with an incidental finding of desmoid-type fibromatosis of the abdomen with recurrence within two years and required surgical interventions. Primarily, a computed tomography (CT) of the abdomen and pelvis showed an incidental finding of a large soft tissue mass in the right iliac fossa mesentery measuring 11 by 8.5 cm. The patient underwent a successful elective exploratory laparotomy and resection of the mass along with a small bowel. A final pathology revealed the mass to be a primary desmoid of the small bowel. Despite clear resection margins, the patient developed recurrence after 17 months, which was treated with surgical resection. His post-operative course was uneventful. The patient's clinical presentation, management, and diagnosis are discussed in this case report.
Authors
- Sangara Narayanasamy
- Ali Yasen Mohamedahmed (ORCID: https://orcid.org/0000-0002-1219-7571)
- Stelios Vakis
- Jyotsna Kakarla
- Shuhaini Musa
Institutions
- Burton Hospitals NHS Foundation Trust (GB)
Publication Details
- Journal
- Cureus
- Published
- 2024-09-10
- DOI
- https://doi.org/10.7759/cureus.69049
- Citations
- 1
- Primary Topic
- Soft tissue tumor case studies
- Type
- article
- Field-Weighted Citation Impact
- 0.47