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Abstract
Desmoid’s tumours (DTs) are rare neoplasm arising from fascial or deep musculo-aponeurotic structures.
They are localized in the abdominal wall, the bowel, and the mesenteryn (associated with familial adenomatous polyposis) or in extra-abdominal sites, such as the trunk and the extremities.
The incidence of DTs ranges from 2% to 4% per million; almost Optimal management has not been clearly defined.
Surgery is generally considered
the treatment mainstay.