JUVENILE GRANÜLOSA CELL TUMOUR OF OVARY: CASE REPORT

Volume: 40 Number: 2 June 1, 2001
  • Hurşit Apa
  • Safiye Aktaş
  • Berrin Ergüven
  • Ragıp Ortaç
  • İrfan Karaca
  • Müge Özalp
  • Canan Vergin
EN TR

JUVENILE GRANÜLOSA CELL TUMOUR OF OVARY: CASE REPORT

Abstract

The sex-cord stromal tumors of the ovary comprise 5% of ali ovarian cancers. Some endocrine changes lıke puberty precocs, amenorrhea, vırilisation may associate. A 22 month old female with juvenile granulosa celi tumor of ovary is presented. She had puberty precocs and abdominal mass. A suprapubic painless mass (12x11x9 cm) was detected during clinical examination and abdominal ultrasonography. The mass was mobile and encapsulated with well defined round borders. Right salphingooopherectomy was performed. Macroscopically the mass was solid. lobular, white-qray in color and encapsulated. On microscopic examination, the neoplastic granulosa cells were arranged in nodules, clusters or cords. Foci of edema and microcystic changes were observed. The Kİ-67 activity was found to be low and P53 negative. The case was stage la according to FİGO staging system. The endocrine changes regressed during follow-up. The patient is alive and healty during 8 months follow-up.

Keywords

Details

Primary Language

Turkish

Subjects

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Journal Section

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Authors

Hurşit Apa

Safiye Aktaş

Berrin Ergüven

Ragıp Ortaç

İrfan Karaca

Müge Özalp

Canan Vergin

Publication Date

June 1, 2001

Submission Date

June 1, 2001

Acceptance Date

-

Published in Issue

Year 1970 Volume: 40 Number: 2

Vancouver
1.Hurşit Apa, Safiye Aktaş, Berrin Ergüven, Ragıp Ortaç, İrfan Karaca, Müge Özalp, Canan Vergin. OVER KÖKENLİ JUVENİL GRANÜLOSA HÜCRELİ TÜMÖR : OLGU SUNUMU. EJM [Internet]. 2001 Jun. 1;40(2):141-3. Available from: https://izlik.org/JA37JU39JE

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