Literature DB >> 17987807

Mesenteric fibromatosis. Case report.

A Giuliani1, M Demoro, A Ciardi, M Scimó, F Galati, M T Lonardo, G Galati.   

Abstract

Deep fibromatosis is a rare locally aggressive but not metastasizing proliferation. Intra-abdominal fibromatosis (IAF) occurs either in association with Gardner's syndrome or as a sporadic event and presents in most cases differential diagnostic problems with myofibroblastic or fibroblastic tumors, characterized by a more aggressive biological behaviour such as gastrointestinal stromal tumors (GISTs). In absence of loco-regional and/or distant metastasis differential diagnosis may be difficult and represents a topical issue, since it influences treatment choice. We describe the case of a patient with sporadic IAF in which the tumor locally involved the mesentery and presented no loco-regional and distant spread. On histology, some morphological features of the neoplasm were in common with a GIST. Definitive diagnosis was made, postoperatively, on the basis of immunohistochemical findings.

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Year:  2007        PMID: 17987807

Source DB:  PubMed          Journal:  J Exp Clin Cancer Res        ISSN: 0392-9078


  2 in total

1.  Mesenteric fibromatosis (desmoid tumour) - a rare case report.

Authors:  Mukut D; Hemanth Sureshwara Ghalige; Santhosh R; M Birkumar Sharma; Th Sudhir Chandra Singh
Journal:  J Clin Diagn Res       Date:  2014-11-20

2.  Rare acute abdominal condition caused by mesenteric fibromatosis perforation: A case report.

Authors:  Jian Li; Run Xu; Deng-Min Hu
Journal:  Medicine (Baltimore)       Date:  2019-01       Impact factor: 1.889

  2 in total

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