A Rare Case of Poorly-Differentiated Sertoli Leydig Cell Tumour of Ovary with Mesenchymal Heterology ED07-ED09
Dr. Archana Khade,
Department of Pathology, 1nd Floor, 'C' Wing,
HBT Medical College and Dr.R.N. Cooper Hospital, Juhu, Mumbai-56, Maharashtra, India.
Sertoli–Leydig Cell Tumours (SLCT) accounts for less than 0.5% of all ovarian neoplasms. Presence of mesenchymal heterologous elements in a poorly differentiated SLCT is extremely uncommon. It not only causes diagnostic difficulty but also renders an aggressive behaviour to the tumour. We report a rare case of poorly differentiated SLCT with cartilage and rhabdomyoblastic differentiation along with review of literature.