Steroid Cell Tumour of Ovary – A Rare Case Report
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 constit...
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doaj-9c59381b87ce4a69b842a06b9b447ff02020-11-25T03:23:28ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2016-09-01109ED06ED0710.7860/JCDR/2016/15767.8556Steroid Cell Tumour of Ovary – A Rare Case ReportRanjeev Bhagat0Vijay Kumar Bodal1Nishit Gupta2Pooja Garg3Assistant Professor, Department of Pathology, Government Medical College and Hospital, Chandigarh, India.Associate Professor, Department of Pathology, Government Medical College, Patiala, Punjab, India.Junior Resident, Department of Pathology, Government Medical College Patiala, India.Junior Resident, Department of Pathology, Government Medical College Patiala, India.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. https://jcdr.net/articles/PDF/8556/15767_CE[Ra]_F(P)_PF1(AHPRAK)_PFA(AK).pdfadnexal massandrogenicpost-menopausal |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ranjeev Bhagat Vijay Kumar Bodal Nishit Gupta Pooja Garg |
spellingShingle |
Ranjeev Bhagat Vijay Kumar Bodal Nishit Gupta Pooja Garg Steroid Cell Tumour of Ovary – A Rare Case Report Journal of Clinical and Diagnostic Research adnexal mass androgenic post-menopausal |
author_facet |
Ranjeev Bhagat Vijay Kumar Bodal Nishit Gupta Pooja Garg |
author_sort |
Ranjeev Bhagat |
title |
Steroid Cell Tumour of Ovary – A Rare Case Report |
title_short |
Steroid Cell Tumour of Ovary – A Rare Case Report |
title_full |
Steroid Cell Tumour of Ovary – A Rare Case Report |
title_fullStr |
Steroid Cell Tumour of Ovary – A Rare Case Report |
title_full_unstemmed |
Steroid Cell Tumour of Ovary – A Rare Case Report |
title_sort |
steroid cell tumour of ovary – a rare case report |
publisher |
JCDR Research and Publications Private Limited |
series |
Journal of Clinical and Diagnostic Research |
issn |
2249-782X 0973-709X |
publishDate |
2016-09-01 |
description |
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. |
topic |
adnexal mass androgenic post-menopausal |
url |
https://jcdr.net/articles/PDF/8556/15767_CE[Ra]_F(P)_PF1(AHPRAK)_PFA(AK).pdf |
work_keys_str_mv |
AT ranjeevbhagat steroidcelltumourofovaryararecasereport AT vijaykumarbodal steroidcelltumourofovaryararecasereport AT nishitgupta steroidcelltumourofovaryararecasereport AT poojagarg steroidcelltumourofovaryararecasereport |
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1724606100182925312 |