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卵巢混合性中胚叶肿瘤:基于组织发生学考虑的免疫组织化学研究

Mixed mesodermal tumor of the ovary: immunohistochemical study with histogenetic consideration.

作者信息

Haba R, Kobayashi S, Miki H, Hirakawa E, Mori S, Ohmori M, Handou T, Shiota A, Ishii Y

机构信息

First Department of Pathology, Kagawa Medical School, Japan.

出版信息

Acta Pathol Jpn. 1993 Nov;43(11):696-701. doi: 10.1111/j.1440-1827.1993.tb02555.x.

Abstract

The clinical, histological and immunohistochemical features of three cases of ovarian mixed mesodermal tumor (MMT) were examined. The epithelial component was serous papillary cystadenocarcinoma in case 1 and 3, and endometrioid adenocarcinoma in case 2. In case 1, undifferentiated adenocarcinoma was also seen. The mesenchymal component was fibrosarcomatous and chondrosarcomatous in case 1 and 2. In case 3, only fibrosarcomatous area was seen. No endometriosis was observed. Immunohistochemically, the epithelial component showed positivity for epithelial membrane antigen in all three cases. S-100 protein was positive in two cases with chondrosarcomatous differentiation. The fibrosarcomatous area showed positivity for vimentin in all three cases. However desmin, myosin and myoglobin were negative. The antibodies thought to be epithelial or mesenchymal markers unexpectedly reacted positively in some cells; for example, EMA was positive in fibrosarcomatous and chondrosarcomatous cells. Therefore, it was speculated that because the undifferentiated tumor cells had a biphasic character, MMT might originate from immature multipotential cells of surface epithelium and subcapsular connective tissue of the ovary.

摘要

对三例卵巢混合性中胚叶肿瘤(MMT)的临床、组织学和免疫组化特征进行了检查。病例1和3的上皮成分是浆液性乳头状囊腺癌,病例2是子宫内膜样腺癌。病例1还可见未分化腺癌。病例1和2的间叶成分是纤维肉瘤样和软骨肉瘤样。病例3仅见纤维肉瘤样区域。未观察到子宫内膜异位症。免疫组化方面,所有三例的上皮成分上皮膜抗原均呈阳性。S-100蛋白在两例有软骨肉瘤样分化的病例中呈阳性。所有三例的纤维肉瘤样区域波形蛋白均呈阳性。然而,结蛋白、肌球蛋白和肌红蛋白均为阴性。一些被认为是上皮或间叶标志物的抗体在某些细胞中意外地呈阳性反应;例如,EMA在纤维肉瘤样和软骨肉瘤样细胞中呈阳性。因此,推测由于未分化肿瘤细胞具有双相特征,MMT可能起源于卵巢表面上皮和被膜下结缔组织的未成熟多潜能细胞。

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