Abstract
Overin juvenil granüloza hücreli tümörleri nadir görülen tümörlerdir. Klinik olarak endokrin sendromlar, pelvik kitle ve asit ile ortaya çıkarlar. Makroskobik olarak solid, solid-kistik ya da tamamen kistik olabilirler. Olgumuz 20 yaşında kadın hasta olup karında şişlik nedeni ile hastanemize başvurmuştur. Abdominal ultrasonografide sağ overde 23 cm çapında kistik kitle saptanan hasta opere edilerek adneksiyel kitle eksize edilmiştir. Kitlenin histopatolojik incelemesi sonucu juvenil granüloza hücreli tümör tanısı konulmuştur.
Keywords
Abstract
Juvenile granulosa cell tumors of the ovary are rare. Clinically, endocrine syndromes are seen associated with a pelvic mass and ascites. On gross examination the juvenile granulosa cell tumor may be entirely solid, solid and cystic or entirely cystic. Our case is a 20-year-old female who was admitted to the hospital due to abdominal swelling. Abdominal ultrasonography showed a 23 cm cystic mass in the right ovary. With laparotomy the right adnexal cystic mass was excised. Histologic examination of the surgical specimen revealed juvenile granulosa cell tumor.
Keywords
Details
| Other ID | JA83VH74TN |
|---|---|
| Journal Section | Case Report |
| Authors | |
| Publication Date | January 1, 2004 |
| Submission Date | January 1, 2004 |
| Published in Issue | Year 2004 Volume: 7 Issue: 1 |