ArticleJournal of clinical and diagnostic research : JCDR2014
Mesenteric fibromatosis (desmoid tumour) - a rare case report.
Article in Journal of clinical and diagnostic research : JCDR, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 17 citations in OpenAlex.
- Twist of fate: Acute small-bowel volvulus caused by a giant mesenteric desmoid-type fibromatosis: A case report and literature review.Radiology case reports · 2026Article
- A rare case of perforated giant mesenteric fibromatosis causing acute peritonitis.Journal of surgical case reports · 2025Article
- A clinician's perspective on the new organ mesentery and non-vascular mesenteropathies.Frontiers in physiology · 2024Review
- Solitary mesenteric fibromatosis in a male patient: clinical case report.Journal of surgical case reports · 2023Article
- Large desmoid tumour of the small bowel mesentery.BMJ case reports · 2022Article
- Ball in the Wall: Mesenteric Fibromatosis-a Rare Case Report.Indian journal of surgical oncology · 2020Article
- Isolated flat desmoid-type terminal ileal mesenteric fibromatosis masquerading as lower ureteric stricture-an intraoperative surprise.Turkish journal of urology · 2019Article
- Desmoid Tumor as an Initial Presentation of Familial Adenomatous Polyposis: A Review of the Literature.Cureus · 2018Review
- Primary Desmoid-Type Fibromatosis of the Mesentery: Report of an Unusual Tumor Localization.Journal of gastrointestinal cancer · 2018Article
- Aggressive Fibromatosis of the Left Mesocolon Mimicking a Gastrointestinal Stromal Tumor: A Case Report.Case reports in oncologyArticle
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mesenteric Fibromatosis (MF) is a proliferative fibroblastic lesion of small intestinal mesentery. It constitutes 8% of all desmoid tumours, which represent 0.03% of all neoplasm. It is histologically benign but may invade locally and recur after excision. It occurs sporadically or in association with Familial adenomatous polyposis (FAP) mutation as a component of Gardner's syndrome. The presenting features of MF are asymptomatic abdominal mass, abdominal discomfort or pain, bowel or ureteral obstruction, intestinal perforation, fistula, functional impairment of ileoanal anastomosis following colectomy in FAP cases. A 29-year-old male presented with a swelling on the right side of the umbilicus for six months and dull aching pain for two months. Fine needle aspiration cytology, ultrasonography, contrast enhanced computerized tomography findings were inconclusive. After Exploratory laparotomy, a mass approx 6x5x4 cm in ileal mesentery was identified and excised along with 20cm of ileum. End to end anastomosis was done and specimen was sent for histopathology which confirmed the diagnosis of MF. Considering the rarity of this tumour and difficulties in diagnostic and therapeutic ambit, we believe it is justified to describe this case which came to our observation.
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