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Updated: Jan 31, 2026

Multimodality Diagnosis of Mesenteric Ischemia

Multimodality Diagnosis of Mesenteric Ischemia

Published on: July 21, 2023

Mesenteric Fibromatosis.

V Radhakrishna¹, R S Patil²

¹Department Paediatric Surgery, Indira Gandhi Institute of Child Health, Bengaluru, India.

Kathmandu University Medical Journal (KUMJ)

|December 24, 2018

Summary

This summary is machine-generated.

Mesenteric fibromatosis is a rare benign tumor that can invade organs. This case highlights primary mesenteric fibromatosis in a young female, successfully treated with surgical excision.

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Area of Science:

Gastroenterology
Surgical Oncology
Pathology

Background:

Mesenteric fibromatosis is a rare, locally invasive benign tumor originating from mesenteric fibroblasts.
While often associated with Gardner's Syndrome or estrogen intake, it can occur primarily.
Its infiltrative growth poses a risk of fatal visceral involvement.

Observation:

A 19-year-old female presented with abdominal mass and pain.
Initial diagnosis suggested a subserous fibroid.
Further evaluation revealed primary mesenteric fibromatosis.

Findings:

The patient underwent wide surgical excision of the mesenteric fibromatosis.
Adjacent bowel resection was performed concurrently.
Post-operative follow-up showed no evidence of tumor recurrence.

Implications:

This case underscores the importance of considering primary mesenteric fibromatosis in young females with abdominal masses.
Wide surgical excision is an effective treatment modality.
Complete resection can lead to favorable long-term outcomes without recurrence.