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Ewha Med J. 2012 Mar;35(1):49-53. Korean. Case Report. https://doi.org/10.12771/emj.2012.35.1.49
Noh KT , Sung SH , Lee RA .
Department of Surgery, Ewha Womans University School of Medicine, Seoul, Korea. ralee@ewha.ac.kr
Department of Pathology, Ewha Womans University School of Medicine, Seoul, Korea.
Abstract

Desmoid tumor is rare neoplasm originated from fibrous sheath or musculoaponeurotic structure. It is classified as benign tumor histologically, but clinically, it has malignant characteristics due to its infiltrative growth to adjacent organ and frequent local recurrence. Especially, mesenteric desmoid tumor shows poor prognosis because of its symptoms of pain, intestinal obstruction, ureter obstruction and fistula formation and high frequency of recurrence. We experienced a case of mesenteric desmoid tumor in a 64-year-old woman with a painless abdominal mass. Laparoscopic exploration was performed and 10 cm sized mesenteric mass was identified, which resected widely and the diagnosis was confirmed with desmoid tumor by pathologic report. We reviewed the feature of the mesenteric desmoid tumor, that is, pathophysiology, clinical presentations, diagnosis, treatment and prognosis.

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