A Rare Case of Poorly-Differentiated Sertoli Leydig Cell Tumour of Ovary with Mesenchymal Heterology
Published: August 1, 2018 | DOI: https://doi.org/10.7860/JCDR/2018/34407.11922
Rahul Pandey, Yasmeen Khatib, Vinita Pandey, Archana Khade, Manisha Khare
1. Ex-Registrar, Department of Pathology, TATA Memorial Hospital, Parel, Mumbai, Maharashtra, India.
2. Associate Professor, Department of Pathology, HBT Medical College and Dr. R.N. Cooper Hospital, Juhu, Mumbai, Maharashtra, India.
3. Ex Speciality Medical Officer, Department of Pathology, HBT Medical College and Dr. R.N. Cooper Hospital, Juhu, Mumbai, Maharashtra, India.
4. Assistant Professor, Department of Pathology, HBT Medical College and Dr. R.N. Cooper Hospital, Juhu, Mumbai, Maharashtra, India.
5. Professor, Department of Pathology, HBT Medical College and Dr. R.N. Cooper Hospital, Juhu, Mumbai, Maharashtra, India.
Correspondence
Dr. Archana Khade,
Department of Pathology, 1nd Floor, C Wing,
HBT Medical College and Dr. R.N. Cooper Hospital, Juhu, Mumbai-56, Maharashtra, India.
E-mail: arck115@gmail.com
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.
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