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Malignant mixed müllerian tumor of primary mesenteric origin associated with a synchronous ovarian cancer: case report and literature review
1Departments of Surgery, Kaohsiung Municipal Hsiao-Kang Hospital, Taiwan
2Departments of Pathology, Kaohsiung Municipal Hsiao-Kang Hospital, Taiwan
3Department of Pathology, Kaohsiung Chang Gung Memorial Hospital, Taiwan
4Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan
5Departments of Anesthesia, Kaohsiung Municipal Hsiao-Kang Hospital, Taiwan
6Departments of Obstetrics and Gynecology, Kaohsiung Municipal Hsiao-Kang Hospital, Taiwan
7Departments of Surgery, Kaohsiung Medical University Hospital, Taiwan
*Corresponding Author(s): J.Y. Wang E-mail: cy614112@ms14.hinet.net
Malignant mixed mullerian tumor (MMMT) is a rare tumor in females and extragenital MMMT is even more so. We report a patient with MMMT primarily in the mesentery with synchronous ovarian cancer. In the English literature, 42 cases of extragenital MMMT have been reported other than the presented case, and this is only the second MMMT arising from the mesentery. Furthermore, among the cases reviewed, MMMTs tend to be associated with synchronous or metachronous colonic cancer or gynecologic tumors originating from the mullerian duct, including ovarian tumors, fallopian tube cancer, endometrial cancer, cervical cancer, and serous carcinoma of the peritoneum (14 Out of 43 patients; 32.6%). The risk factors for MMMT include obesity, nulliparity, exogenous estrogen, and long-term tamoxifen use. The prognosis of MMMT is catastrophic and the treatment is based oil the experience of those of uterine sarcomas, which is composed of operation, radiotherapy and chemotherapy.
Malignant mixed müllerian tumor; Mesentery; Ovarian cancer
C.J. Ma,S.F. Yang,C.C. Huang,C.Y. Chai,K.I. Cheng,E.M. Tsai,J.Y. Wang. Malignant mixed müllerian tumor of primary mesenteric origin associated with a synchronous ovarian cancer: case report and literature review. European Journal of Gynaecological Oncology. 2008. 29(3);289-293.
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