SMALL CELL CARCINOMA OF THE OVARY OF HYPERCALCEMIC TYPE: A RARE TUMOR

Authors

  • Varun Goel Rajiv Gandhi Cancer Institute and Research Centre, Rohini Delhi
  • Chandragouda Dgouda Rajiv Gandhi Cancer Institute and Research Centre, Rohini Delhi
  • Sajjan Singh Rajiv Gandhi Cancer Institute and Research Centre, Rohini Delhi
  • Shubhra Raina Rajiv Gandhi Cancer Institute and Research Centre, Rohini Delhi
  • Vineet Talwar Rajiv Gandhi Cancer Institute and Research Centre, Rohini Delhi
  • Nivedita Patnaik University College of Medical Sciences and Guru Teg Bahadur Hospital, Delhi
  • Sunil Pasricha University College of Medical Sciences and Guru Teg Bahadur Hospital, Delhi

Keywords:

Small Cell Carcinoma, Ovary, Hypercalcemic Type, Immunohistochemistry, chemotherapy

Abstract

Small Cell Carcinoma of the Ovary of Hypercalcemic Type (SCCOHT) is a rare entity. Very few cases have been reported to date. Most literature about SCCOHT is isolated clinico-pathological series and case reports. We report a case of SCCOHT in a 40 year old female with a pre-operative diagnosis of bilateral ovarian complex cysts. The pa- tient underwent left ovarian cystectomy with right ovarian biopsy and histopathological examination revealed fea- tures of a poorly differentiated carcinoma with intervening extensive areas of necrosis (upto 80%). Tumor cells were positive for EMA, CK, CK7 (focally) CD10, synaptophysin and vimentin hence confirming the diagnosis of SCCOHT. Post surgery patient was started on Etoposide and cisplatin based adjuvant chemotherapy. In view of highly aggressive nature of this tumor, prompt diagnosis and imparting effective chemotherapy regimen to the pa- tient is required.

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Published

2014-03-31

How to Cite

Goel, V. ., Dgouda, C. ., Singh, S. ., Raina, S. ., Talwar, V. ., Patnaik, N., & Pasricha, S. . (2014). SMALL CELL CARCINOMA OF THE OVARY OF HYPERCALCEMIC TYPE: A RARE TUMOR. National Journal of Medical Research, 4(01), 113–115. Retrieved from https://njmr.in/index.php/file/article/view/478

Issue

Section

Case Report