Sclerosing stromal tumor of the ovary: A case report

Year 2017, Volume: 48 Issue: 3, 103 - 106, 10.09.2017

Gonca Oğurlu Pakay , Kaan Pakay , Canan Kabaca Kocakuşak Ateş Karateke , Özden Us Hatice Öztürkmen , Ecmel Kaygusuz

https://doi.org/10.16948/zktipb.272955

Abstract

Classified among ovarian sex cord tumors, sclerosing stromal tumor
(SST) is an extremely rare ovarian malignant tumor which occurs predominantly
between the ages of 20 to 40.  However small number of postmenopausal or childhood cases were reported.

Lower abdomen USG and pelvic MRI indicated unilateral heterogen
cyctic mass in the 13 year old patient who presented to hospital with
complaints of dysmenorrhoea and abnormal uterine hemorrage. This article covers
imaging, operation, histopathological properties and distinctive diagnosis of
the benign sclerosing stromal tumors (SST).

Keywords

adolescent, ovarian

OVERİN SKLEROZAN STROMAL TÜMÖRÜ: OLGU SUNUMU

Abstract

Overin sklerozan
stromal tümörü (SST),  over seks  kord tümörleri içinde sınıflandırılan ve
oldukça nadir görülen benign karakterli bir tümördür. Bu tümörler çoğunlukla  20-40 yaş 
aralığında görülürler,  ancak az
sayıda olguda postmenopozal dönemde ya da çocukluk döneminde görülebilirler.

     13 yaşında anormal uterin kanama  ve dismenore 
yakınması ile başvuran 
adolesan  kızda, alt batın
ultrasonografisi  (USG)  ve pelvik manyetik rezonans görüntülemede
(MRG)  unilateral heterojen kistik kitle
tespit edilmiştir. Bu makalede benign sklerozan stromal tümör olgusunun,
görüntüleme, operasyon, histopatolojik özellikleri ve ayırıcı tanısı
sunulmuştur.

Keywords

adolesan, over

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