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伴有甲胎蛋白异位产生的卵巢子宫内膜样腺癌。

Ovarian endometrioid adenocarcinoma with ectopic production of alpha-fetoprotein.

作者信息

Maida Y, Kyo S, Takakura M, Kanaya T, Inoue M

机构信息

Department of Obstetrics and Gynecology, School of Medicine, Kanazawa University, 13-1, Takaramachi, Ishikawa, Kanazawa, 920-0934, Japan.

出版信息

Gynecol Oncol. 1998 Oct;71(1):133-6. doi: 10.1006/gyno.1998.5119.

Abstract

alpha-Fetoprotein (AFP) is well known as a tumor marker of ovarian endodermal sinus tumor or embryonal carcinoma in gynecological malignancies. However, AFP production is extremely rare in ovarian epithelial cancers. Here we report a case of a 53-year-old woman with an AFP-producing ovarian endometrioid adenocarcinoma. The serum AFP level was elevated up to 2759 ng/ml preoperatively, with a subsequent decrease to the normal range after treatment. Histological examination of the tumor revealed a well-differentiated endometrioid adenocarcinoma with small foci of clear cell components. None of endodermal sinus tumor, hepatoid carcinoma, or embryonal carcinoma components were observed. Immunohistochemical analysis revealed that AFP was expressed in the cytoplasm of the endometrioid glandular lesions, but not in the clear cell components. This is probably the first case of a pure type of ovarian endometrioid adenocarcinoma with significant levels of AFP expression.

摘要

甲胎蛋白(AFP)作为妇科恶性肿瘤中卵巢内胚窦瘤或胚胎癌的肿瘤标志物广为人知。然而,AFP在卵巢上皮癌中的产生极为罕见。在此,我们报告一例53岁产生AFP的卵巢子宫内膜样腺癌女性病例。术前血清AFP水平升高至2759 ng/ml,治疗后随后降至正常范围。肿瘤的组织学检查显示为高分化子宫内膜样腺癌,伴有小灶性透明细胞成分。未观察到内胚窦瘤、肝样癌或胚胎癌成分。免疫组织化学分析显示,AFP在内膜样腺性病变的细胞质中表达,但在透明细胞成分中不表达。这可能是首例具有显著AFP表达水平的纯型卵巢子宫内膜样腺癌病例。

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