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
. 2013 Oct;47(5):472-6.
doi: 10.4132/KoreanJPathol.2013.47.5.472. Epub 2013 Oct 25.

Abdominal fibromatosis in a young child: a case study and review of the literature

Affiliations

Abdominal fibromatosis in a young child: a case study and review of the literature

Hyun Hee Chu et al. Korean J Pathol. 2013 Oct.

Abstract

Fibromatoses comprise many different entities of well-differentiated fibroblastic proliferation with variable collagen production and form a firm nodular mass. Abdominal fibromatosis is distinguishable from other forms of fibromatosis because of its location and its tendency to occur in women of childbearing age during or following pregnancy. Abdominal fibromatosis in children is an extremely rare condition. A 15-month-old boy presented with an abdominal wall mass that had recently increased in size. Mass excision was perfomed. The tumor was 4.3×4.1 cm and partly circumscribed. Histologically, the tumor was composed of parallel long fascicles of spindle-cells with a uniform appearance. The edges of the resected mass were infiltrative, and the surgical margins were positive. Mitotic figures were <1/10 high power fields. No cellular atypia or necrosis was present. The tumor cells were positive for vimentin and nuclear β-catenin staining.

Keywords: Abdominal wall; Child; Fibromatosis.

PubMed Disclaimer

Conflict of interest statement

No potential conflict of interest relevant to this article was reported.

Figures

Fig. 1
Fig. 1
The cut section of the abdominal tumor reveals a grayish-white solid mass with partially irregular edges (arrows).
Fig. 2
Fig. 2
Histologic findings. (A, B) The tumor reveals long fascicles of bland spindle-shaped fibroblasts with collagen deposition. (C) The tumor shows infiltrative growth and the surgical margins are positive. (D, E) The tumor cells show nuclear and cytoplasmic β-catenin immunostaining.

Similar articles

Cited by

References

    1. Weiss SW, Goldblum JR. Enzinger and Weiss's soft tissue tumors. Philadelphia: Mosby Elsevier; 2008. pp. 277–302.
    1. Ademuyiwa AO, Bode CO, Elebute OA. Anterior abdominal wall desmoids tumor in a five year old girl: a pre operative diagnostic challenge in resource-poor setting. Ann Pediatr Surg. 2010;6:41–43.
    1. Atahan IL, Akyol F, Zorlu F, Gürkaynak M. Radiotherapy in the management of aggressive fibromatosis. Br J Radiol. 1989;62:854–856. - PubMed
    1. Ayala AG, Ro JY, Goepfert H, Cangir A, Khorsand J, Flake G. Desmoid fibromatosis: a clinicopathologic study of 25 children. Semin Diagn Pathol. 1986;3:138–150. - PubMed
    1. Buitendijk S, van de Ven CP, Dumans TG, et al. Pediatric aggressive fibromatosis: a retrospective analysis of 13 patients and review of literature. Cancer. 2005;104:1090–1099. - PubMed

LinkOut - more resources