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Ovarian Steroid Cell Tumour: Correlation of Histopathology with Clinicopathologic Features

Ovarian steroid cell tumours (not otherwise specified) are rare neoplasms of the ovary and are classified under lipid cell tumours. Their diagnosis can be considered as one of exclusion. Histopathologically, the tumour should carefully be evaluated for microscopic features of malignancy, but it is e...

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Autores principales: Mehdi, Ghazala, Ansari, Hena A., Sherwani, Rana K., Rahman, Khaliqur, Akhtar, Nishat
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049327/
https://www.ncbi.nlm.nih.gov/pubmed/21436872
http://dx.doi.org/10.4061/2011/987895
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author Mehdi, Ghazala
Ansari, Hena A.
Sherwani, Rana K.
Rahman, Khaliqur
Akhtar, Nishat
author_facet Mehdi, Ghazala
Ansari, Hena A.
Sherwani, Rana K.
Rahman, Khaliqur
Akhtar, Nishat
author_sort Mehdi, Ghazala
collection PubMed
description Ovarian steroid cell tumours (not otherwise specified) are rare neoplasms of the ovary and are classified under lipid cell tumours. Their diagnosis can be considered as one of exclusion. Histopathologically, the tumour should carefully be evaluated for microscopic features of malignancy, but it is essential for the clinician and the pathologist to remember that in these tumours, pathologically benign histomorphology does not exclude the possibility of clinically malignant behaviour. Our case study focuses on the comparative findings in a postmenopausal female diagnosed with an ovarian steroid tumour (not otherwise specified). A careful correlation between clinical and surgical evaluation and microscopic analysis is necessary, as is a regular followup.
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spelling pubmed-30493272011-03-24 Ovarian Steroid Cell Tumour: Correlation of Histopathology with Clinicopathologic Features Mehdi, Ghazala Ansari, Hena A. Sherwani, Rana K. Rahman, Khaliqur Akhtar, Nishat Patholog Res Int Case Report Ovarian steroid cell tumours (not otherwise specified) are rare neoplasms of the ovary and are classified under lipid cell tumours. Their diagnosis can be considered as one of exclusion. Histopathologically, the tumour should carefully be evaluated for microscopic features of malignancy, but it is essential for the clinician and the pathologist to remember that in these tumours, pathologically benign histomorphology does not exclude the possibility of clinically malignant behaviour. Our case study focuses on the comparative findings in a postmenopausal female diagnosed with an ovarian steroid tumour (not otherwise specified). A careful correlation between clinical and surgical evaluation and microscopic analysis is necessary, as is a regular followup. SAGE-Hindawi Access to Research 2011-03-02 /pmc/articles/PMC3049327/ /pubmed/21436872 http://dx.doi.org/10.4061/2011/987895 Text en Copyright © 2011 Ghazala Mehdi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mehdi, Ghazala
Ansari, Hena A.
Sherwani, Rana K.
Rahman, Khaliqur
Akhtar, Nishat
Ovarian Steroid Cell Tumour: Correlation of Histopathology with Clinicopathologic Features
title Ovarian Steroid Cell Tumour: Correlation of Histopathology with Clinicopathologic Features
title_full Ovarian Steroid Cell Tumour: Correlation of Histopathology with Clinicopathologic Features
title_fullStr Ovarian Steroid Cell Tumour: Correlation of Histopathology with Clinicopathologic Features
title_full_unstemmed Ovarian Steroid Cell Tumour: Correlation of Histopathology with Clinicopathologic Features
title_short Ovarian Steroid Cell Tumour: Correlation of Histopathology with Clinicopathologic Features
title_sort ovarian steroid cell tumour: correlation of histopathology with clinicopathologic features
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049327/
https://www.ncbi.nlm.nih.gov/pubmed/21436872
http://dx.doi.org/10.4061/2011/987895
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