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Revista chilena de cirugía

versión On-line ISSN 0718-4026

Resumen

BAROTTO, MARTÍN et al. Mesenteric fibromatosis: Report of one case. Rev Chil Cir [online]. 2008, vol.60, n.6, pp.557-560. ISSN 0718-4026.  http://dx.doi.org/10.4067/S0718-40262008000600014.

Desmoid tumor or mesenteric fibromatosis is an uncommon disease with to variants: a sporadic form and one associated to familial adenomatous polyposis. Surgery is the treatment of choice. We report a 45 years oíd male presenting with abdominal pain and fever. An abdominal ultrasound informed the presence of a mass in the periumblical área. An Abdominal CAT sean showed a 13 cm diameter solid mass located in the left upper quadrant. The patient was operated and that mass is excised, requiring also a hemicolectomy, excisión of the fourth portion of the duodenum and cholecystectomy. The pathology report of the excised tumor informs a mesenteric fibromatosis. The patient was discharged at the 18th postoperative day.

Palabras clave : Abdominal mass; desmoids tumor; mesenteric fibromatosis.

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