| Literature DB >> 27790445 |
Ranjeev Bhagat1, Vijay Kumar Bodal2, Nishit Gupta3, Pooja Garg3.
Abstract
Steroid cell tumours of the ovary are uncommon sex- hormone secreting tumours characterized by a steroid cell proliferation. The incidence of steroid cell tumour of the ovary is only 0.1% of all ovarian tumours. As far as steroid cell tumours, not otherwise specified (NOS) is concerned; it constitutes about 56% of all steroid cell tumours. Here we present a case of 55-year-old, postmenopausal patient who presented with complaints of bleeding per vaginum and abdominal pain for last 3-4 months, with history of excessive hair growth since 3-4 years. Ultrasonography revealed a solid right ovarian mass with a possibility of ovarian sex cord tumour. Histopathology confirmed the diagnosis of steroid cell tumour NOS type with no cytological atypia.Entities:
Keywords: Adnexal mass; Androgenic; Post-menopausal
Year: 2016 PMID: 27790445 PMCID: PMC5071945 DOI: 10.7860/JCDR/2016/15767.8556
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X