Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2024 Sep 10;16(9):e69049.
doi: 10.7759/cureus.69049. eCollection 2024 Sep.

A Rare Case of Recurrent Intra-abdominal Desmoid-Type Fibromatosis

Affiliations
Case Reports

A Rare Case of Recurrent Intra-abdominal Desmoid-Type Fibromatosis

Shuhaini Musa et al. Cureus. .

Abstract

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.

Keywords: desmoid tumours; desmoid-type fibromatosis; fibroblasts; intra-abdominal mass; spindle-shaped cells.

PubMed Disclaimer

Conflict of interest statement

Human subjects: Consent was obtained or waived by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Figures

Figure 1
Figure 1. CT abdomen and pelvis (coronal section labelled A and sagittal section labelled B) demonstrating the mass in the right iliac fossa (red arrows).
Figure 2
Figure 2. Histopathology slide images of the resected mass. The top slide image (labelled A) is H&E-stained and shows sweeping fascicles of uniform spindle cells (magnification: 40×). The bottom slide (labelled B)image shows positive results with immunohistochemistry for beta-catenin (magnification: 20×).
H&E: hematoxylin and eosin
Figure 3
Figure 3. CT abdomen and pelvis (coronal section labelled A and sagittal section labelled B) demonstrating the mass in the left iliac fossa (red arrows).

References

    1. Current update on desmoid fibromatosis. Ganeshan D, Amini B, Nikolaidis P, Assing M, Vikram R. J Comput Assist Tomogr. 2019;43:29–38. - PMC - PubMed
    1. A to Z of desmoid tumors. Shinagare AB, Ramaiya NH, Jagannathan JP, Krajewski KM, Giardino AA, Butrynski JE, Raut CP. AJR Am J Roentgenol. 2011;197:0–14. - PubMed
    1. Desmoid tumor: analysis of prognostic factors and outcomes in a surgical series. Mullen JT, Delaney TF, Kobayashi WK, et al. Ann Surg Oncol. 2012;19:4028–4035. - PubMed
    1. Postoperative recurrence of desmoid tumors: clinical and pathological perspectives. Wang YF, Guo W, Sun KK, Yang RL, Tang XD, Ji T, Tang S. World J Surg Oncol. 2015;13:26. - PMC - PubMed
    1. Intra-abdominal fibromatosis: differentiation from gastrointestinal stromal tumour based on biphasic contrast-enhanced CT findings. Zhu H, Chen H, Zhang S, Peng W. Clin Radiol. 2013;68:1133–1139. - PubMed

Publication types

LinkOut - more resources