{"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 , Obuhovich Anneta Romualdovna , 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}
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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.