Literature DB >> 15937804

Mesenteric fibromatosis in a young girl without familial adenomatous polyposis.

Sergio Huerta1, David R Heubner, Daniel R Marcus.   

Abstract

Mesenteric fibromatosis (MF) is a rare, benign tumor commonly associated with Gardner's syndrome. The signs and symptoms in patients with MF are insidious. Patients may present with abdominal pain or discomfort when the tumors reach large sizes, which is typical at the time of diagnosis. Differentiating MF from other neoplasms such as gastrointestinal stromal tumors may present a diagnostic dilemma, especially in patients without any history of familial adenomatous polyposis. In the present report, we discuss a young girl who presented with MF. A pertinent review of the literature is also presented. This case is peculiar in that MF presented at a young age in a patient without history of familial adenomatous polyposis and occurred in the omentum with local invasion to the stomach.

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Year:  2005        PMID: 15937804     DOI: 10.1016/j.jpedsurg.2005.02.017

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  2 in total

1.  Mesenteric fibromatosis causing ureteral stenosis.

Authors:  Jae Young Choi; Kyung Mo Kang; Bum Soo Kim; Tae-Hwan Kim
Journal:  Korean J Urol       Date:  2010-07-20

2.  Gradually shrinking intra-abdominal desmoid tumor derived from the stomach in a young boy: a case report.

Authors:  Kazushi Miyata; Masahide Fukaya; Masato Nagino
Journal:  Surg Case Rep       Date:  2017-04-20
  2 in total

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