Overin nadir tümörü: sklerozan stromal tümör
Year 2020,
, 449 - 452, 14.05.2020
Soner Gök
,
Erkan Alataş
,
Ender Düzcan
Abstract
Overin sklerozan stromal tümörü oldukça nadir
görülen benign nonepitelyal bir tümördür. Hastalar genellikle pelvik ağrı, adet
düzensizliği ve ele gelen kitle nedeniyle başvururlar. Bazen de hormonal olarak
aktif olup androjen fazlalığı semptomlarına yol açabilmektedir. Tümörün radyolojik
görüntüsü ve makroskopisindeki solid yapılar malign izlenim verebilmektedir. Kesin
tanısı çoğunlukla postoperatif histolojik inceleme ile konulmaktadır. Biz bu
olgu sunumunda oldukça nadir görülen sklerozan stromal tümörün klinik ve
histopatolojik özelliklerini ve olgu yönetimini sunmayı amaçladık.
References
- 1- Scully RE, Young RH, and Clement PB. Tumors of the ovary Mal developed gonads, fallopian tube and broad ligament. Washington, DC: Pathology A FIo, 1998.
- 2- Tavassoli FA, Fujii S, Mooney E, et al. Sexcord-stromal tumors In: Tumours of the Breast and Female Genital organs. 5. ed. IARC Press: Lyon: 2003; p. 152-153.
- 3- Iravanloo G, Nozarian Z, Sarrafpour B, Motahhary P. Sclerosing stromal tumor of the ovary. Arch Iran Med 2008;11:561-562.
- 4- Qureshi A, Raza A, Kayani N. The morphologic and immunohistoochemical spectrum of 16 cases of sclerosing stromal tumor of theovary. Indian J Pathol Microbiol 2010;53:658-660.
- 5- Aktaş S, Diniz G, Ortaç R, Ergin M. Sclerosing stromal tumor of the ovary with precocious puberty in a seven month old girl: Case Report. Turkiye Klinikleri J Gynecol Obst 2009;19(2):98-101.
- 6- Young RH, Clement PB. Sexcord-stromal and steroid cell and germ cell tumors of the ovary. In: Mills S, editor. Sternberg’s Diagnostic Surgical Pathology, Volume II. 5th ed. Lippincott Williams and Wilkins 2010; p. 2315-2316.
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Rare tumor of the ovary: sclerosing stromal tumor.
Year 2020,
, 449 - 452, 14.05.2020
Soner Gök
,
Erkan Alataş
,
Ender Düzcan
Abstract
Sclerosing stromal tumor of the ovary is a very
rare benign nonepithelial tumor. Patients usually present with pelvic pain,
menstrual irregularity and palpable mass. Sometimes it is hormonal active and
can cause symptoms of excess androgen. Radiological appearance of the tumor and
solid structures in macroscopy can give a malignant impression. The definitive
diagnosis is usually made by postoperative histological examination. In this
case report, we aimed to present the clinical and histopathological features
and case management of a very rare sclerosing stromal tumor.
References
- 1- Scully RE, Young RH, and Clement PB. Tumors of the ovary Mal developed gonads, fallopian tube and broad ligament. Washington, DC: Pathology A FIo, 1998.
- 2- Tavassoli FA, Fujii S, Mooney E, et al. Sexcord-stromal tumors In: Tumours of the Breast and Female Genital organs. 5. ed. IARC Press: Lyon: 2003; p. 152-153.
- 3- Iravanloo G, Nozarian Z, Sarrafpour B, Motahhary P. Sclerosing stromal tumor of the ovary. Arch Iran Med 2008;11:561-562.
- 4- Qureshi A, Raza A, Kayani N. The morphologic and immunohistoochemical spectrum of 16 cases of sclerosing stromal tumor of theovary. Indian J Pathol Microbiol 2010;53:658-660.
- 5- Aktaş S, Diniz G, Ortaç R, Ergin M. Sclerosing stromal tumor of the ovary with precocious puberty in a seven month old girl: Case Report. Turkiye Klinikleri J Gynecol Obst 2009;19(2):98-101.
- 6- Young RH, Clement PB. Sexcord-stromal and steroid cell and germ cell tumors of the ovary. In: Mills S, editor. Sternberg’s Diagnostic Surgical Pathology, Volume II. 5th ed. Lippincott Williams and Wilkins 2010; p. 2315-2316.
- 7- Russell P, Robboy SJ, Prat J. Ovarian sexcord-stromal and steroid cell tumors. In: Robboy’s Pathology of the Female Reproductive Tract, 2nd ed. Churchill Living stone Elsevier 2009; p. 703-705.