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一名绝经后女性的息肉样子宫内膜腺肌瘤,酷似宫颈癌,与卵巢卵泡膜瘤相关。

Polypoid endometrial adenomyoma in a postmenopausal woman, mimicking cervical cancer, associated with ovarian thecoma.

作者信息

Horn L-C, Fischer U, Höckel M

机构信息

Institute of Pathology, University of Leipzig, Liebigstrasse 26, D-04103 Leipzig, Germany.

出版信息

Arch Gynecol Obstet. 2002 Dec;267(2):101-3. doi: 10.1007/s00404-001-0253-8.

Abstract

PURPOSE

Atypical polypoid adenomyoma (APA) usually occurs in premenopausal women and arises from the endometrium. APAs protruding into the external os may lead to diagnostic problems.

CASE

We present a case of APA in a 62-year-old postmenopausal woman, prolapsing through the external os, clinically mimicking cervical cancer FIGO IB2 (4.5 cmx3 cmx3 cm). Histologically the tumor was composed of endometrioid-like with slight cellular atypia and endocervical-type mucinous glands admixed with smooth muscle bundles, exhibiting low Ki-67 antigen immunostaining. The the left adnexa contained an ovarian thecoma.

CONCLUSIONS

To the best of our knowledge, this is the first case of APA in a postmenopausal woman, mimicking cervical cancer and associated with ovarian thecoma. Pathogenetically it is proposed, that hyperestrogenism and, in the present case accompanied by progestin production of questionable source, may play an important role in the development of APAs with the admixture of endometrial and endocervical glands.

摘要

目的

非典型息肉样腺肌瘤(APA)通常发生于绝经前女性,起源于子宫内膜。突出于外口的APA可能导致诊断困难。

病例

我们报告一例62岁绝经后女性的APA病例,该肿瘤经外口脱出,临床上酷似国际妇产科联盟(FIGO)IB2期宫颈癌(4.5 cm×3 cm×3 cm)。组织学上,肿瘤由具有轻微细胞异型性的子宫内膜样组织和宫颈内膜型黏液腺混合平滑肌束组成,Ki-67抗原免疫染色呈低表达。左侧附件区有一个卵巢卵泡膜瘤。

结论

据我们所知,这是首例绝经后女性的APA病例,酷似宫颈癌并伴有卵巢卵泡膜瘤。从发病机制来看,高雌激素状态,在本病例中伴有来源不明的孕激素产生,可能在伴有子宫内膜和宫颈内膜腺体混合的APA发生发展中起重要作用。

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