IMR Press / EJGO / Volume 31 / Issue 4 / pii/1630985270107-2059608638

European Journal of Gynaecological Oncology (EJGO) is published by IMR Press from Volume 40 Issue 1 (2019). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on as a courtesy and upon agreement with S.O.G.

Case Report
Malignant mixed mullerian tumor of the cervix including components of a rhabdomyosarcoma: case report and literature review
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1 Division of Gynecologic Oncology, Department of Obstetrics and Gynecology and Hospital Pathology, Seoul St. Mary’s Hospital The Catholic University of Korea Seoul (Republic of Korea)
Eur. J. Gynaecol. Oncol. 2010, 31(4), 462–466;
Published: 10 August 2010

Malignant mixed mesodermal tumors (MMMTs) are composed of carcinomatous and sarcomatous components and have an aggressive metastatic potential, resulting in a poor prognosis. MMMTs of gynecologic origin typically arise from either the ovary or the uterus, and MMMTs of the cervix are extremely rare. Due to the rarity of MMMTs arising from the cervix, there is no consensus regarding treatment, prognosis, and outcome; however, aggressive surgical cytoreduction, combined with adjuvant platinumbased chemotherapy and/or radiotherapy, is recommended as the treatment of choice for MMMTs of the cervix. Cervical MMMTs are more often confined to the uterus at the time of diagnosis and frequently have non-glandular epithelial components. For these reasons, MMMTs of the cervix may have a better prognosis compared to the uterine counterparts. A case of an immunohistochemically confirmed primary MMMT of the cervix, including components of a rhabdomyosarcoma, is reported.
Malignant mixed mesodermal tumor
Cervical cancer
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