Ito K
Department of Obstetrics and Gynecology, Kinki University School of Medicine, Osaka-Sayama, Japan.
Tohoku J Exp Med. 1994 Jan;172(1):51-7. doi: 10.1620/tjem.172.51.
Mixed mesodermal tumor (MMT) arising from the ovary is very rare, but we recently encountered two cases of this tumor. The tumors were examined histologically using hematoxylin-eosin, alcian blue, periodic acid-Schiff (PAS), and toluidine blue staining, as well as immunohistochemical staining for S-100 protein. The two patients were postmenopausal women aged 68 and 58 years, respectively. The carcinomatous region of the mixed tumor was endometrioid carcinoma in Patient 1 and serous cystadenocarcinoma in Patient 2, while the sarcomatous region was chondrosarcoma in both patients. The chondrosarcoma tissue was positive for PAS, alcian blue, toluidine blue, and S-100 protein.
起源于卵巢的混合性中胚层肿瘤(MMT)非常罕见,但我们最近遇到了两例这种肿瘤。使用苏木精-伊红、阿尔辛蓝、过碘酸希夫(PAS)和甲苯胺蓝染色以及S-100蛋白免疫组化染色对肿瘤进行了组织学检查。两名患者分别为68岁和58岁的绝经后女性。病例1混合肿瘤的癌性区域为子宫内膜样癌,病例2为浆液性囊腺癌,而两名患者的肉瘤区域均为软骨肉瘤。软骨肉瘤组织对PAS、阿尔辛蓝、甲苯胺蓝和S-100蛋白呈阳性。