Sclerosing stromal tumor: a rare ovarian neoplasm
Yükleniyor...
Tarih
2022
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Sclerosing stromal tumor (SST) is an extremely rare and distinctive sex cord stromal tumor, which occurs predominantly in the second and third decades of life. SSTs make up 2-6% of ovarian sex-cord stromal tumors. Due to the solid and distinct vascular structure of the tumor, it can be mistaken as a number of malignant ovarian tumors. As this specific neoplasm is very rare, it is not always possible to diagnose the tumor preoperatively with clinical and ultrasonographic findings. Furthermore, histopathological and immunohistochemical analysis does not always confirm the diagnosis. In this case report, clinical findings, histopathological features, and macroscopic appearance during laparoscopy of an SST are presented in a 20-year-old woman with pelvic pain. SST should be considered among the differential diagnosis of women with adnexal masses.
Açıklama
Anahtar Kelimeler
Benign Ovarian Neoplasm, Laparoscopy, Sclerosing Stromal Tumor
Kaynak
J Turk Ger Gynecol Assoc .
WoS Q Değeri
N/A
Scopus Q Değeri
N/A
Cilt
23
Sayı
1
Künye
Kadiroğulları P, Seçkin KD. Sclerosing stromal tumor: a rare ovarian neoplasm. J Turk Ger Gynecol Assoc. 2022 Mar 8;23(1):68-70.
