Abstract
Steroid hücreli tümörler over tümörlerinin %0,1 ini oluflturan
nadir görülen tümörlerdir.Sınıflandırılamayan steroid hücreli tümörler
ise steroid hücreli tümörlerin en sık görülen alt tipidir. Bu
makalede, histerektomi ve bilateral salpingooferektomi sonras›nda
insidental olarak saptanan bir sınıflandırılamayan steroid hücreli
tümör olgusu sunulmaktadır. Bu olgu sunumunda amacımız nadir
görülen bir over tümörü olan sınıflandırılamayan steroid hücreli
tümörlere dikkat çekmektir
References
- 1. Scully RE, Young RH, Clement PB. Atlas of Tumor Pathology Tumors of the Ovary, Maldeveloped Gonads, Fallopian Tube, and Broad Ligament, Armed Forces Institute of Pathology, Washington DC 1998
- 2. Scully RE, Young RH Sex Cord-Stromal, Steroid Cell, and Germ Cell Tumors of the Ovary. Glob. libr. women’s med. 2008;1756-2228
- 3. Hayes MC, Scully RE. Ovarian Steroid Cell Tumors (Not Otherwise Specified): A Clinicopathological Analysis of 63 Cases Am J Surg Pathol 1987;11(11):835- 45
- 4. Ulukufl Ç, Koyuncuo¤lu M, Özen E, Erten O. Steroid Hücreli Tümör (Lipid Hücreli Tümör) Bir Olgu Sunumu Türkiye Klinikleri Jinekol Obst 2003;13:322-4
- 5. Roth LM. Recent Advances in the Pathology and Classification of Ovarian Sex CordYStromal Tumors International Journal of Gynecological Pathology 2006;25:199-215
- 6. Hayes MC, Scully RE. Stromal luteoma of the ovary: a clinicopathological analysis of 25 cases. Int J Gynecol Pathol 1987;6:313-21
- 7. Jones MW, Harri R, Dabbs DJ, Carter GJ. Immunoh›stochemical profile of steroid cell tumor of the ovary: a study of 14 cases and areview of the literature Int J Gynecol Pathol 2010;29(4):315-20
- 8. Ye L, Wu XL, Xu L, Huang Q, Sun L, He Y, Yang KX. Ovarian steroid cell tumor, not otherwise specifed:a clinicopathologic study Zhonghua Bing Li Xue Za Zhi. 2007;36(8):516-20
Abstract
Steroid cell tumors of the ovary are rare, accounting 0.1%of all
ovarian tumors. Steroid cell tumor-NOS is the most common subtype
of steriod cell tumors. In this study, we report a case which was diagnosed
as steroid cell tumor-nos incidentally after histerectomy and
bilateral salpingo-oophorectomy. The goal of this case report is to
reemphasise this rare ovarian tumor steroid cell tumor-NOS.
References
- 1. Scully RE, Young RH, Clement PB. Atlas of Tumor Pathology Tumors of the Ovary, Maldeveloped Gonads, Fallopian Tube, and Broad Ligament, Armed Forces Institute of Pathology, Washington DC 1998
- 2. Scully RE, Young RH Sex Cord-Stromal, Steroid Cell, and Germ Cell Tumors of the Ovary. Glob. libr. women’s med. 2008;1756-2228
- 3. Hayes MC, Scully RE. Ovarian Steroid Cell Tumors (Not Otherwise Specified): A Clinicopathological Analysis of 63 Cases Am J Surg Pathol 1987;11(11):835- 45
- 4. Ulukufl Ç, Koyuncuo¤lu M, Özen E, Erten O. Steroid Hücreli Tümör (Lipid Hücreli Tümör) Bir Olgu Sunumu Türkiye Klinikleri Jinekol Obst 2003;13:322-4
- 5. Roth LM. Recent Advances in the Pathology and Classification of Ovarian Sex CordYStromal Tumors International Journal of Gynecological Pathology 2006;25:199-215
- 6. Hayes MC, Scully RE. Stromal luteoma of the ovary: a clinicopathological analysis of 25 cases. Int J Gynecol Pathol 1987;6:313-21
- 7. Jones MW, Harri R, Dabbs DJ, Carter GJ. Immunoh›stochemical profile of steroid cell tumor of the ovary: a study of 14 cases and areview of the literature Int J Gynecol Pathol 2010;29(4):315-20
- 8. Ye L, Wu XL, Xu L, Huang Q, Sun L, He Y, Yang KX. Ovarian steroid cell tumor, not otherwise specifed:a clinicopathologic study Zhonghua Bing Li Xue Za Zhi. 2007;36(8):516-20
Details
| Other ID | JA93AE44HA |
|---|---|
| Journal Section | Research Article |
| Authors | |
| Publication Date | October 1, 2011 |
| Submission Date | October 1, 2011 |
| Published in Issue | Year 2011 Volume: 14 Issue: 4 |