Author/Authors :
Bairwa, Shilpa Dept of Pathology - SHKM - GMC, Nalhar - Mewat - Haryana - India , Satarkar, Rahul Narayan Dept of Pathology - SHKM - GMC, Nalhar - Mewat - Haryana - India , Kalhan, Shivani Dept of Pathology - SHKM - GMC, Nalhar - Mewat - Haryana - India , Garg, Shilpa Dept of Pathology - SHKM - GMC, Nalhar - Mewat - Haryana - India , Sangwaiya, Ashok Dept of Pathology - SHKM - GMC, Nalhar - Mewat - Haryana - India , Singh, Pawan Dept of Pathology - SHKM - GMC, Nalhar - Mewat - Haryana - India
Abstract :
Ovarian sex cord-stromal tumors are relatively infrequent neoplasms that account
for approximately 8% of all primary ovarian neoplasm. Sex cord-stromal tumors of
the ovary include granulosa cell tumors, fibrothecomas, Sertoli-Leydigcell tumors,
steroid cell tumors, and sclerosing stromal tumors (SST). Sclerosing stromal tumors
account for 2% to 6% of ovarian stromal tumors. Despite the rarity of this particular
neoplasm, it is not always possible to predict the presence of this tumor
preoperatively on the basis of clinical and sonographic findings. Histopathological
and immunohistochemical (IHC) examinations confirm the diagnosis. Herein, the
clinical findings and histopathological features of SST are described in a 24-year-old
female
