• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一名患有多囊卵巢综合征的女性的分泌雄激素的成年颗粒细胞瘤:病例报告

Androgen-secreting adult granulosa cell tumor in a woman with polycystic ovary syndrome: a case report.

作者信息

Gu Chongjuan, Zeng Xiaoqin, Shi Quan, Xiao Qing, He Yaojuan

机构信息

Department of Obstetrics and Gynecology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

Pathology department, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

出版信息

Gynecol Endocrinol. 2022 Nov;38(11):1014-1016. doi: 10.1080/09513590.2022.2143491. Epub 2022 Nov 11.

DOI:10.1080/09513590.2022.2143491
PMID:36367302
Abstract

To present the clinicopathologic findings of the second case of androgen-secreting adult granulosa cell tumor (AGCT) in a woman with polycystic ovary syndrome (PCOS) and discuss in the light of the literature. Description of a case and discussion of the literature. A patient with oligomenorrhea, amenorrhea and hirsutism who was diagnosed as PCOS and treated by oral contraceptive for three years, then left ovarian solid and liquid mass was found and pathologically confirmed to be androgen-secreting AGCT after left oophorectomy. She got regular menstrual cycle and gave birth naturally, but clinical features of PCOS reappeared after breastfeeding. Androgen-secreting AGCT and PCOS have similar clinical features of hyperandrogenism, it is difficult to diagnose androgen-secreting AGCT when both diseases occur in the same patient. If the size of cystic mass in androgen-secreting AGCT is too small to differentiate from PCOM on imaging, pathological examination after surgery may be the only way to find the disease.

摘要

介绍一名患有多囊卵巢综合征(PCOS)的女性中第二例分泌雄激素的成人颗粒细胞瘤(AGCT)的临床病理结果,并结合文献进行讨论。病例描述与文献讨论。一名患有月经过少、闭经和多毛症的患者,被诊断为PCOS并接受口服避孕药治疗三年,随后发现左侧卵巢有实性和液性肿块,左侧卵巢切除术后病理证实为分泌雄激素的AGCT。她月经周期恢复正常并自然分娩,但母乳喂养后PCOS的临床特征再次出现。分泌雄激素的AGCT和PCOS具有相似的高雄激素血症临床特征,当两种疾病发生在同一患者身上时,很难诊断出分泌雄激素的AGCT。如果分泌雄激素的AGCT中囊性肿块的大小太小,在影像学上无法与多囊卵巢(PCOM)区分开来,手术后进行病理检查可能是发现该疾病的唯一方法。

相似文献

1
Androgen-secreting adult granulosa cell tumor in a woman with polycystic ovary syndrome: a case report.一名患有多囊卵巢综合征的女性的分泌雄激素的成年颗粒细胞瘤:病例报告
Gynecol Endocrinol. 2022 Nov;38(11):1014-1016. doi: 10.1080/09513590.2022.2143491. Epub 2022 Nov 11.
2
Increasing hirsutism due to a granulosa-cell tumor in a woman with polycystic ovary syndrome: case report and review of the literature.多囊卵巢综合征女性因颗粒细胞瘤导致多毛症:病例报告及文献复习。
Gynecol Endocrinol. 2013 Apr;29(4):273-7. doi: 10.3109/09513590.2012.743012. Epub 2013 Jan 18.
3
MORE THAN MEETS THE EYE IN A PATIENT WITH PCOS: ANDROGEN-SECRETING GRANULOSA CELL OVARIAN TUMOR IN A VIRILIZED WOMAN WITH POLYCYSTIC OVARIAN SYNDROME (PCOS).多囊卵巢综合征(PCOS)患者的情况比表面所见更为复杂:一名患有PCOS的男性化女性出现分泌雄激素的颗粒细胞瘤。
AACE Clin Case Rep. 2020 Apr 3;6(4):e170-e173. doi: 10.4158/ACCR-2019-0576. eCollection 2020 Jul-Aug.
4
Testosterone elevation in ovarian adult granulosa cell tumor: A case report and review of the literature.卵巢成人颗粒细胞瘤中睾酮升高:病例报告及文献复习。
Medicine (Baltimore). 2023 May 12;102(19):e33763. doi: 10.1097/MD.0000000000033763.
5
AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS, AMERICAN COLLEGE OF ENDOCRINOLOGY, AND ANDROGEN EXCESS AND PCOS SOCIETY DISEASE STATE CLINICAL REVIEW: GUIDE TO THE BEST PRACTICES IN THE EVALUATION AND TREATMENT OF POLYCYSTIC OVARY SYNDROME--PART 1.美国临床内分泌医师协会、美国内分泌学会以及雄激素过多与多囊卵巢综合征协会疾病状态临床综述:多囊卵巢综合征评估与治疗最佳实践指南——第1部分。
Endocr Pract. 2015 Nov;21(11):1291-300. doi: 10.4158/EP15748.DSC.
6
A case report of ovarian granulosa cell tumor in patient with polycystic ovarian syndrome.多囊卵巢综合征患者卵巢颗粒细胞瘤 1 例报告。
Medicine (Baltimore). 2021 Dec 17;100(50):e28261. doi: 10.1097/MD.0000000000028261.
7
Characteristics of in vitro steroidogenesis in a woman with hyperandrogenism, a granulosa cell tumor and polycystic ovary disease. A case report.一名患有高雄激素血症、颗粒细胞瘤和多囊卵巢疾病女性的体外类固醇生成特征。病例报告。
J Reprod Med. 1988 Apr;33(4):377-81.
8
AMH producing purely cystic virilizing adult granulosa cell tumor in 17 years old girl: a case report and review of literatures.17 岁女孩单纯性囊泡型分泌 AMH 的成人颗粒细胞瘤:病例报告及文献复习
J Ovarian Res. 2023 Mar 15;16(1):52. doi: 10.1186/s13048-023-01134-0.
9
[Sertoli-Leydig cell tumour (arrhenoblastoma) in a patient with polycystic ovary syndrome: clinical, ultrasonographic, hormonal and histopathological evaluation].[多囊卵巢综合征患者的支持-间质细胞瘤(男性细胞瘤):临床、超声、激素及组织病理学评估]
Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:51-5.
10
Androgenic adult granulosa cell tumor in a 13-year-old prepubertal patient: a case report and review of the literature.一名13岁青春期前患者的成人型雄激素化颗粒细胞瘤:病例报告及文献复习
Int J Gynecol Pathol. 2000 Jul;19(3):266-71. doi: 10.1097/00004347-200007000-00011.

引用本文的文献

1
Adult-type granulosa cell tumor associated with elevated luteinizing hormone: Two rare case reports.成人型颗粒细胞瘤伴促黄体生成素升高:两例罕见病例报告。
Medicine (Baltimore). 2024 Feb 16;103(7):e37069. doi: 10.1097/MD.0000000000037069.
2
AMH producing purely cystic virilizing adult granulosa cell tumor in 17 years old girl: a case report and review of literatures.17 岁女孩单纯性囊泡型分泌 AMH 的成人颗粒细胞瘤:病例报告及文献复习
J Ovarian Res. 2023 Mar 15;16(1):52. doi: 10.1186/s13048-023-01134-0.