Abstract
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.
Keywords
References
- 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
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
Keywords
References
- 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
Details
| Other ID | JA93TJ95YV |
|---|---|
| Journal Section | Research Article |
| Authors | |
| Publication Date | July 1, 2014 |
| Submission Date | July 1, 2014 |
| Published in Issue | Year 2014 Volume: 17 Issue: 3 |