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Mesenteric fibromatosis (also called intra-abdominal desmoid tumor) is a rare, benign but locally aggressive fibroblastic proliferation arising from the mesenteric connective tissue. Although non-metastasizing, it shows infiltrative growth and a high tendency for local recurrence.

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Etiopathogenesis


Clinical Features


Radiology


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CT/MRI show an infiltrative mesenteric mass encasing vessels/loops.

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Modality Imaging features
US Hypoechoic, ill-defined intra-abdominal/mesenteric mass.
CT • Well-defined but infiltrative soft-tissue mass in mesentery.
• Homogeneous attenuation (iso- to slightly hyperdense vs muscle).
• Variable enhancement: mild to moderate, progressive.
• May encase bowel loops and vessels without causing obstruction (distinguishes from lymphoma which encases but is homogeneous).
• Can cause kinking/narrowing of small bowel → obstruction.
MR • T1: Iso- to hypointense to muscle.
• T2: Variable – may be hypointense due to collagen (mature lesions), or hyperintense in cellular/edematous lesions.
• Post-contrast: moderate heterogeneous enhancement.
• Helps assess relation to vessels and bowel, and follow-up.
PET-CT Generally low to moderate FDG uptake (less than high-grade sarcomas or lymphoma).

Differentials