A rare case report of Sertoli Leydig cell tumour of ovary

Sertoli-Leydig cell tumor (SLCTs) of the ovary, also known as androblastoma, is a rare neoplasm from group sex cord-stromal tumors ovary. They account for less than 0.5% all ovarian tumors. typically occur in young and reproductive women patients usually present with abdominal swelling or pain. A case 35-year-old multiparous female presented mass, ultrasonography revealed large abdomino-pelvic complex solid cystic mass lesion arising left She underwent staging laparotomy followed by total hysterectomy salpingo-ovariotomy right salpingo-oopherectomy partial omentectomy. Histopathological examination (HPE) features suggestive moderately differentiated SLCT ovary (with heterologous elements).