CASE REPORT
Inflammatory Myofibroblastic Tumor of the Appendix
Takahisa Hirokawa1)3), Minoru Yamamoto1)4), Masaki Sakamoto1), Hirozumi Sawai1), Hiromitsu Takeyama1), Tadao Manabe1)4) and Satoru Takahashi2)
Department of Gastroenterological Surgery1) and Department of Experimental Pathology and Tumor Biology2), Nagoya City University Graduate School of Medical Sciences
National Cancer Center Hospital3)
Department of Surgery, Kariya Toyota General Hospital4)
Colorectal inflammatory myofibroblastic tumors (IMT) are rare, and most commonly occur in the lung. We report a case of IMT of the appendix, involving a malignant tumor in the differential diagnosis based on the speed of tumor growth. A 58-year-old man admitted for alcoholic cirrhosis had a growing tumor palpable in the lower right quadrant. Enhanced abdominal CT showed a slightly contrasted mass around the cecum. No tumor was found by colonoscopy without external compression. Barium enema findings indicated diverticuli of the ascending colon and deformation of the cecum, suggesting an inflammatory tumor whose malignancy could not be excluded, necessitating so laparoscopy-assisted ileocecal resection. The postoperative pathological diagnosis was IMT.
Key words
inflammatory myofibroblastic tumor (IMT), inflammatory pseudotumor (IPT), appendix
Jpn J Gastroenterol Surg 41: 446-451, 2008
Reprint requests
Takahisa Hirokawa National Cancer Center Hospital
5-1-1 Tsukiji, Chuo-ku, 104-0045 JAPAN
Accepted
October 19, 2007
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