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Journals / Journal of Surgery and Medicine / 2026 / Cilt: 3 Sayı: 10

Extraovarian granulosa cell tumor: A case report

Abdelouhab El Marouni(Visceral Surgey Service, Hassan II University Hospital,Faculty of Medicine and pharmacy of Fez, Morocco)0000-0003-2035-7982
Karam Aziz(Visceral Surgey Service, Hassan II University Hospital,Faculty of Medicine and pharmacy of Fez, Morocco)0000-0002-3330-7311
İmane Toghrai(Visceral Surgey Service, Hassan II University Hospital,Faculty of Medicine and pharmacy of Fez, Morocco)0000-0003-0401-3012
Khalid Mazaz(Visceral Surgey Service, Hassan II University Hospital,Faculty of Medicine and pharmacy of Fez, Morocco)0000-0001-7779-7802
Karim Ibn Majdoub(Visceral Surgey Service, Hassan II University Hospital,Faculty of Medicine and pharmacy of Fez, Morocco)0000-0002-0421-7296
Pages
772–773
Publication Date
2019-10-01
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We herein present a case of extraovarian granulosa tumor, the clinical and therapeutic aspects, and our approach.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Granulosa cell tumor (GCT) of the ovary is a rare tumor representing 2 to 5% of all ovarian neoplasms.
📊
Key Findings & Data:It can reproduce or metastasize several years after the initial treatment.
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Conclusion & Impact:We herein present a case of extraovarian granulosa tumor, the clinical and therapeutic aspects, and our approach.
🔬Design:Olgu Sunumu
📍Scope:Comprehensive Sample
⚙️Variables:Ekstraovaryan · Granulosa hücreli tümör · Histolojik tanı

Abstract

Granulosa cell tumor (GCT) of the ovary is a rare tumor representing 2 to 5% of all ovarian neoplasms. It can reproduce or metastasize several years after the initial treatment. In rare cases, CGT can develop on an extra-ovarian site, which is thought to originate from ectopic gonadal tissue along the embryonic genital ridge. We herein present a case of extraovarian granulosa tumor, the clinical and therapeutic aspects, and our approach.

Özet

Overin granuloza hücreli tümörü (GCT), tüm over neoplazmalarının %2-5'ini oluşturan nadir bir tümördür. Tedaviden birkaç yıl sonra yeniden ortaya çıkabilir veya metastaz yapabilir. Sık olmamakla birlikte, embriyonik genital katlantı üzerindeki ektopik gonadal dokudan köken alarak, ekstra-overyen bir bölgede de görülebilir. Burada bir ekstraovaryen granüloza tümörünü, klinik, terapötik yönleri ve kendi yaklaşımımızla birlikte sunuyoruz.

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Cite This Article

Aziz, K. (2019). Extraovarian granulosa cell tumor: A case report. Journal of Surgery and Medicine, Cilt: 3 Sayı: 10, 772–773. https://doi.org/10.28982/josam.560112

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