Abstract
Amaç: Overin nadir tümörlerinden olan transizyonel hücreli tümörlerin klinik ve patolojik özelliklerini incelemek ve klinik deneyimlerimizi paylaşmak. Yöntem: Kliniğimizde 2005-2014 yılları arasında opere edilmiş ve transizyonel hücreli tümör tanısı koyulmuş olan 18 olgu, bilgisayar ve dosya kayıtlarındaki veriler incelenerek retrospektif olarak analiz edilmiştir. Bulgular: Toplam 18 hastadan, 14 hasta benign brenner tümörü (BT) (%71), 1 hasta malign BT, 3 hasta ise transizyonel hücreli karsinomu idi. Benign hastaların %64'ü (9/14), malign hastaların %75 (3/4)'i postmenopozaldi. Benign BT olan hastaların %78,5 (11/14)'i, farklı nedenlerle histerektomi yapılırken, ya da histopatolojik incelemede insidental olarak saptanmış, yalnızca 3 hasta (%21.5) preoperatif adneksiyel kitle tanısı ile prezente olmuştur. Sonuç: Oldukça nadir görülen bu tümörlerin benign formları sıklıkla insidental olarak saptanırken malign tümörlerin prezentasyonu klasik epitelyal over karsinomu şeklinde olmaktadır.
Abstract
Aim: To analyse transitional cell tumors which are the rare tumors of the ovary according to their clinical and pathological features. Method: Eighteen patients with the diagnosis of ovarian transitional cell tumors were identified between 2005 and 2014. Patients were analysed through patients file and computerized data system retrospectively. Results: Fourteen of the eighteen patients (71,5%) were benign brenner tumor (BT), one patient was malign brenner tumor and three patients were transitionel cell tumor of the ovary. 64% (9/14) of the patients with benign hystology and 75% (3/4) of the patients with malign hystology were postmenauposal. 78,5% (11/14) of the patients with benign brenner tumor, detected incidentally during an operation or hystologic examination. Only 3 of the 14 patients (21.5%) presented with an adnexial mass preoperatively. Conclusion: Frequently benign forms of these uncommon tumors were encountered incidentally and malign forms typically presents with symptoms of classical epithelial ovarian carcinoma.
Details
| Other ID | JA38MZ27GF |
|---|---|
| Journal Section | Case Report |
| Authors | |
| Publication Date | January 1, 2015 |
| Submission Date | January 1, 2013 |
| Published in Issue | Year 2015 Volume: 18 Issue: 1 |