Sarcomatoid carcinoma of the small intestine: a rare and highly aggressive tumor
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ÀÌ»ó¾ï ( Lee Sang-Eok )
Konyang University Hospital Department of Surgery
¹Ú½Å¿µ ( Park Shin-Young )
Konyang University Hospital Department of Pathology
KMID : 0371320120830050321
Abstract
Sarcomatoid carcinoma of the small intestine is an extremely rare malignant neoplasm that usually has a poor prognosis. We report a case of sarcomatoid carcinoma arising in the small intestine in a 62-year-old man who was hospitalized for abdominal pain. Computed tomography revealed wall thickening of the small intestine. The resected specimen showed a gray-whitish solid mass with hemorrhage and necrosis. Microscopically, the tumor was composed of pleomorphic spindle and discohesive polygonal cells with frequent mitosis. No carcinomatous component was recognized. Immunohistochemistry revealed coexpression of cytokeratin and vimentin by the tumor cells, whereas expressions of C-kit, CD34, HMB-45, smooth muscle actin, and desmin were negative. The diagnosis was sarcomatoid carcinoma of the small intestine.
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Small intestine; Sarcomatoid carcinoma
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