Journals / Türk Jinekolojik Onkoloji Dergisi / 2026 / Cilt: 17 Sayı: 3

A RARE CASE REPORT: JUVENILE GRANULOSA CELL TUMOR

NADİR BİR VAKA: JUVENİL GRANÜLOZA HÜCRELİ TÜMÖR

Pages
0–0
Publication Date
2014-07-01
DOI
—
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AI Summary & Key Takeaways

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

Histopathology was compatible with the juvenile granulosa cell tumor

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Ovarian sex cord-stromal tumors are rare.
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Key Findings & Data:The juvenile type comprises 5 percent of all granulosa cell tumors.
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Conclusion & Impact:Histopathology was compatible with the juvenile granulosa cell tumor
🔬Design:Makale
📍Scope:Comprehensive Sample
⚙️Variables:Juvenil granüloza hücreli tümör · Over · Juvenile granulosa cell tumor

Abstract

Ovarian sex cord-stromal tumors are rare. There are two subtypes, adult and juvenile. The juvenile type comprises 5 percent of all granulosa cell tumors. They typically develop before puberty, and thus, are more common among young women. A 22-year-old girl is reported who presented with menstrual disturbances and abdominal tenderness. A pelvic ultrasonography showed a predominantly cystic mass lesion with papillary arising from the left ovary. All tumor markers were normal. The patient underwent mass resection with laparoscopic salpingoophorectomy. Histopathology was compatible with the juvenile granulosa cell tumor

Özet

Overin sex-cord kaynaklı tümörü nadirdir. Bu tümörün juvenil ve adult olmak üzere iki tipi vardır. Juvenil tipi tüm granüloza hücreli tümörlerin %5’ini oluşturur. Tipik olarak puberte öncesi geliştiği için genç kadınlar arasında daha sık görülür. 22 yaşında bir kadın menstrual düzensizlik ve karın ağrısı şikayetleri ile başvurdu. Pelvik ultrasonografide sol over kaynaklı papiller yapı içeren kistik kitle izlendi. Tüm tümör belirteçleri normaldi. Hastaya laparoskopik sol salpingooferektomi uygulandı. Histopatolojisi juvenil granüloza hücreli tümör olarak geldi.

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Cite This Article

Yılmaz, M., İsaoğlu, Ü., Delibaş, İ. B., Gündoğdu, C. (2014). A RARE CASE REPORT: JUVENILE GRANULOSA CELL TUMOR. Türk Jinekolojik Onkoloji Dergisi, Cilt: 17 Sayı: 3, 0–0. https://ajindex.com/articles/1603156

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References (7)

  1. Ovarian cancer incidence in the United States, 1992- 1999. Quirk JT, Natarajan N. Gynecol Oncol. 2005; 97: 519-523.
  2. Schumer ST, Cannistra SA. Granulosa cell tumor of the ovary. J Clin Oncol. 2003; 21: 1180-1189.
  3. Case records of the Massachusetts General Hospital Weekly clinicopathological exercises. Case 22–1982. A nine-year-old girl with virilization and a calcifi ed pelvic mass. N Engl J Med. 1982; 306: 1348–1355
  4. Odicino F, Pecorelli S, Zigliani L, Creasman WT. History of the FIGO cancer staging system. Int J Gynaecol Obstet. 2008; 101: 205-210.
  5. Malmström H, Högberg T, Risberg B, Simonsen E. Granulosa cell tumors of the ovary: prognostic factors and outcome. Gynecol Oncol. 1994; 52: 50-55.
  6. Young RH, Dickersin GR, Scully RE. Juvenile granulosa cell tumor of the ovary. A clinicopathological analysis of 125 cases. Am J Surg Pathol. 1984; 8: 575-596.
  7. Ashnagar A, Alavi S, Nilipour Y, Azma R, Falahati F. Massive ascites as the only sign of ovarian juvenile granulosa cell tumor in an adolescent: a case report and a review of the literature. Case Rep Oncol Med. 2013; 2013: 386725. doi: 10.1155/2013/386725. Epub 2013 Jan 29