Giant primary retroperitoneal granulosa cell tumor in a post-oophorectomy patient: A rare case report and a literature review

Surgery Case Reports Pub Date : 2026-03-01 Epub Date: 2026-02-26 DOI:10.1016/j.sycrs.2026.100174
K.A.Nethuki Akithma Kulasinghe , Obuhovich Anneta Romualdovna , Yauheni Aliaksandravich Stasiukevich
{"title":"Giant primary retroperitoneal granulosa cell tumor in a post-oophorectomy patient: A rare case report and a literature review","authors":"K.A.Nethuki Akithma Kulasinghe ,&nbsp;Obuhovich Anneta Romualdovna ,&nbsp;Yauheni Aliaksandravich Stasiukevich","doi":"10.1016/j.sycrs.2026.100174","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Primary retroperitoneal granulosa cell tumors (GCTs) are exceedingly rare, particularly in patients with prior bilateral oophorectomy, posing significant diagnostic challenges.</div></div><div><h3>Case Presentation</h3><div>A 69-year-old woman with multiple comorbidities and a history of hysterectomy with bilateral oophorectomy presented with a large retroperitoneal mass. Preoperative imaging demonstrated a well-defined fluid collection measuring 142 × 193 × 130 mm in the infra-pancreatic region, along with a tissue mass up to 59 × 50 × 33 mm in the left para-aortic area. These findings were consistent with a retroperitoneal mass. Tumor markers were non-contributory. Intraoperatively, the mass was identified as a giant retroperitoneal cyst and completely drained and excised via laparoscopic drainage and Pfannenstiel laparotomy. The definitive diagnosis was established post-operatively by pathohistological examination, which confirmed the lesion to be a Granulosa Cell Tumor.</div></div><div><h3>Conclusion</h3><div>This case underscores the importance of considering rare extra-gonadal GCTs in the differential diagnosis of retroperitoneal masses, even in post-oophorectomy patients. Complete surgical excision and long-term surveillance remain essential due to the risk of late recurrence.</div></div>","PeriodicalId":101189,"journal":{"name":"Surgery Case Reports","volume":"7 ","pages":"Article 100174"},"PeriodicalIF":0.0000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Surgery Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2950103226000186","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/26 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction

Primary retroperitoneal granulosa cell tumors (GCTs) are exceedingly rare, particularly in patients with prior bilateral oophorectomy, posing significant diagnostic challenges.

Case Presentation

A 69-year-old woman with multiple comorbidities and a history of hysterectomy with bilateral oophorectomy presented with a large retroperitoneal mass. Preoperative imaging demonstrated a well-defined fluid collection measuring 142 × 193 × 130 mm in the infra-pancreatic region, along with a tissue mass up to 59 × 50 × 33 mm in the left para-aortic area. These findings were consistent with a retroperitoneal mass. Tumor markers were non-contributory. Intraoperatively, the mass was identified as a giant retroperitoneal cyst and completely drained and excised via laparoscopic drainage and Pfannenstiel laparotomy. The definitive diagnosis was established post-operatively by pathohistological examination, which confirmed the lesion to be a Granulosa Cell Tumor.

Conclusion

This case underscores the importance of considering rare extra-gonadal GCTs in the differential diagnosis of retroperitoneal masses, even in post-oophorectomy patients. Complete surgical excision and long-term surveillance remain essential due to the risk of late recurrence.
卵巢切除术后巨大原发性腹膜后颗粒细胞瘤:一例罕见病例报告及文献复习
原发性腹膜后颗粒细胞瘤(gct)极为罕见,特别是在既往双侧卵巢切除术的患者中,这给诊断带来了重大挑战。病例介绍:一名69岁女性,患有多种合并症,有子宫切除术和双侧卵巢切除术的病史,在腹膜后发现一个大肿块。术前影像表现一个定义良好的流体测量142 ×  193×130  mm infra-pancreatic地区,连同一个组织质量59 ×50  ×  33毫米左para-aortic区域。这些发现与腹膜后肿块一致。肿瘤标志物无贡献。术中,肿块被确定为巨大的腹膜后囊肿,并通过腹腔镜引流和Pfannenstiel剖腹手术完全引流并切除。术后病理组织学检查明确诊断为颗粒细胞瘤。结论本病例强调了考虑罕见的性腺外gct在腹膜后肿块鉴别诊断中的重要性,即使在卵巢切除术后患者中也是如此。由于晚期复发的风险,完全手术切除和长期观察仍然是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书