Resumo

PARRA-MEDINA, Rafael et al. A Case of Duodenal Leiomyosarcoma. Rev Col Gastroenterol [online]. 2015, vol.30, n.3, pp.351-355. ISSN 0120-9957.

Duodenal leiomyosarcoma is a rare disease with poor prognoses for patients. The disease does not have a clear set of signs and symptoms that allows easy diagnosis. Diagnosis is made on the basis of histopathological identification of a mesenchymal lesion composed of malignant tumor cells and immunohistochemistry positive for smooth muscle actin, desmin, muscle specific actin, calponin and caldesmon. We report a case of a 56 year old woman with primary duodenal leiomyosarcoma which had metastasized to the pancreas and the celiac artery

Palavras-chave : Leiomyosarcoma; duodenum; small intestine; mesenchymal tumors.

        · resumo em Espanhol     · texto em Espanhol | Inglês     · Inglês ( pdf ) | Espanhol ( pdf )