Department of Pathology, Shizuoka City Shimizu Hospital, Miyakami 1231, Shimizu-ku, Shizuoka 424-8636, Japan.
Arch Gynecol Obstet. 2011 Jun;283(6):1403-6. doi: 10.1007/s00404-010-1591-1. Epub 2010 Jul 23.
Ovarian malignant Mullerian mixed tumor (MMMT) (carcinosarcoma) is a relatively rare, very aggressive tumor.
Herein is presented an unusual case of heterologous MMMT with an epithelial element composed predominantly of signet ring cell carcinoma.
A 60-year-old Japanese woman consulted our hospital because of a pelvic mass. Imaging modalities showed a huge tumor of the right ovary. Laparotomy was performed, and frozen section showed a malignant tumor. Therefore, hysterectomy, bilateral salpingo-oophorectomy, lymph node dissection, and omentectomy were performed. On gross examination, the right ovarian tumor was solid, measuring 12 × 13 × 12 cm. The surface was smooth but bosselated. Histologically, the tumor was composed of epithelial and sarcomatous elements. Curiously, the epithelial element was composed predominantly of signet ring cell carcinoma. A small area showed tubular adenocarcinoma and poorly differentiated carcinoma. The sarcomatous element was homologous with spindle cell sarcoma with many mitotic cells. The signet ring cells had mucins. Immunohistochemically, the epithelial element was positive for cytokeratins, EMA, p53, CEA, CA19-9, and Ki-67 (labeling = 75%). The sarcomatous element was positive for vimentin, α-smooth muscle actin, p53, and Ki-67 (labeling = 36%), indicating that it was a leiomyosarcoma. Metastases were found in many lymph nodes and intravascular spaces in the peritoneum; the metastases were composed of epithelial elements.
To the best of our knowledge, there have been no descriptions in the English literature of MMMT composed predominantly of signet ring cell carcinoma. An MMMT in this case, should be differentiated from Krukenberg tumor, metastatic signet ring cell carcinoma, and signet ring stromal tumor.
卵巢恶性苗勒混合瘤(MMMT)(癌肉瘤)是一种相对罕见的、极具侵袭性的肿瘤。
本文报道了一例上皮成分主要由印戒细胞癌组成的罕见异源性 MMMT 病例。
一位 60 岁的日本女性因盆腔肿块就诊于我院。影像学检查显示右侧卵巢有一个巨大的肿瘤。行剖腹探查术,冷冻切片显示为恶性肿瘤。因此,进行了子宫切除术、双侧输卵管卵巢切除术、淋巴结清扫术和网膜切除术。大体检查发现,右侧卵巢肿瘤实性,大小为 12×13×12cm,表面光滑但有结节。组织学上,肿瘤由上皮和肉瘤成分组成。奇怪的是,上皮成分主要由印戒细胞癌组成。小区域显示管状腺癌和低分化癌。肉瘤成分与具有许多有丝分裂细胞的梭形细胞肉瘤同源。印戒细胞含有黏液。免疫组化染色显示,上皮成分阳性表达细胞角蛋白、EMA、p53、CEA、CA19-9 和 Ki-67(标记率 =75%)。肉瘤成分阳性表达波形蛋白、α-平滑肌肌动蛋白、p53 和 Ki-67(标记率 =36%),提示为平滑肌肉瘤。腹膜内许多淋巴结和血管腔内均发现转移灶,转移灶由上皮成分组成。
据我们所知,英文文献中尚无主要由印戒细胞癌组成的 MMMT 报道。本例 MMMT 应与 Krukenberg 瘤、转移性印戒细胞癌和印戒细胞性间质瘤相鉴别。