Shintaku M, Matsumoto T
Department of Pathology, Osaka Red Cross Hospital, 5-53 Fudegasaki, Tennoji, Osaka 543-8555, Japan.
Int J Gynecol Pathol. 2001 Apr;20(2):191-5. doi: 10.1097/00004347-200104000-00013.
A müllerian carcinosarcoma or malignant mesodermal mixed tumor (MMMT) originated from the retroperitoneum of a 51-year-old woman; only two previous similar cases have been reported. The 1,040 gm tumor was found in the left retroperitoneal space; the center of the tumor was extensively liquified. The uterus, fallopian tubes, and ovaries were unremarkable. The histopathological features of the tumor were typical of MMMT, homologous type. The adenocarcinomatous component of the tumor was immunohistochemically positive for cytokeratin 7 and negative for cytokeratin 20. MMMTs arising in extragenital sites are rare, and most of them arise from the peritoneum. The histogenesis of extragenital MMMTs remains speculative, but the origin from the "secondary mullerian system" is most likely.
一名51岁女性的腹膜后发生了1例苗勒管癌肉瘤或恶性中胚叶混合瘤(MMMT);此前仅报道过2例类似病例。在左腹膜后间隙发现一个重达1040克的肿瘤;肿瘤中心广泛液化。子宫、输卵管和卵巢未见异常。肿瘤的组织病理学特征为典型的同源性MMMT。肿瘤的腺癌成分免疫组化显示细胞角蛋白7阳性,细胞角蛋白20阴性。发生于生殖器外部位的MMMT很罕见,其中大多数起源于腹膜。生殖器外MMMT的组织发生仍存在推测,但最有可能起源于“继发苗勒系统”。