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
. 2006 Jun 1:4:27.
doi: 10.1186/1477-7819-4-27.

Mesenteric desmoid tumor of the interposed jejunal pouch after total gastrectomy

Affiliations

Mesenteric desmoid tumor of the interposed jejunal pouch after total gastrectomy

Koichi Tamura et al. World J Surg Oncol. .

Abstract

Background: Desmoid tumor is a rare entity, and most desmoid tumors are located in abdominal wall or extra-abdominal tissues. Occurrence of desmoid tumor in mesentry is extremely rare.

Case presentation: we report a mesenteric desmoid tumor in a 73-years-old woman who had undergone total gastrectomy reconstructed with jejunal pouch interposition for gastric carcinoma. After 1 year, a tumor was originating from mesentery of the interposed jejunal pouch was identified, and the patient underwent resection of the large mass which was found to invade pancreas. Histological examination revealed desmoid tumor.

Conclusion: Desmoid tumor is rare, and it was difficult for the differential diagnosis of desmoid tumor or recurrent tumor.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Computed tomography (CT) shows round-shaped solid mass at the right side of the reconstructed jejunal pouch, and invaded into pancreas (arrow).
Figure 2
Figure 2
Magnetic resonance imaging (MRI) showed a low signal intensity of the mass in both T1-weighted (left) and T2-weighted images (right).
Figure 3
Figure 3
The tumor was an elastic hard and white mass, and the size was 50 × 50 × 63 mm. It originated from the interposed mesenterium.
Figure 4
Figure 4
The tumor was composed of spindle-shaped fibroblasts and copious collagen fibers by hematoxylin and eosin stain (H&E). (A: × 100 B: × 400).

References

    1. Naylor EW, Gardner EJ, Richards RC. Desmoid tumors and mesenteric fibromatosis in Gardner's syndrome:report of kidred 109. Arch Surg. 1979;114:1181–1185. - PubMed
    1. Anika H, Claudia A, Tilmann V, Andreas U, Gabriela M. High-dose tamoxifen and sulindac as fiest-line treatment for desmoid tumors. Cancer. 2004;100:612–620. doi: 10.1002/cncr.11937. - DOI - PubMed
    1. Reitamo JJ, Hayry P, Nykyri E, Saxen E. The desmoid tumor. Incidence, sex, age and anatomical distribution in the Finnish population. Am J Clin Pathol. 1982;77:665–673. - PubMed
    1. Rodriguez-Bigas MA, Mahoney MC, Karakousis CP, Petrelli NJ. Desmoid tumors in patients with familial adenomatous polyposis. Cancer. 1994;74:1270–1274. doi: 10.1002/1097-0142(19940815)74:4<1270::AID-CNCR2820740415>3.0.CO;2-7. - DOI - PubMed
    1. Japanese Gastric Cancer Association . Japanese Classification of Gastric Carcinoma. 2. Tokyo: Kanehara & Co., Ltd.; 1998. - PubMed

LinkOut - more resources