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Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature
Sertoli-Leydig cell tumours of the ovary (SLCT) are rare tumours predominantly caused by mutations in the DICER1 gene. We present a patient with a unilateral SLCT who had an underlying germline DICER1 gene mutation. We discuss the underlying pathology, risks, and screening opportunities available to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176314/ https://www.ncbi.nlm.nih.gov/pubmed/30356399 http://dx.doi.org/10.1155/2018/7927362 |
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author | Wormald, B. Elorbany, S. Hanson, H. Williams, J. W. Heenan, S. Barton, D. P. J. |
author_facet | Wormald, B. Elorbany, S. Hanson, H. Williams, J. W. Heenan, S. Barton, D. P. J. |
author_sort | Wormald, B. |
collection | PubMed |
description | Sertoli-Leydig cell tumours of the ovary (SLCT) are rare tumours predominantly caused by mutations in the DICER1 gene. We present a patient with a unilateral SLCT who had an underlying germline DICER1 gene mutation. We discuss the underlying pathology, risks, and screening opportunities available to those with a mutation in this gene as SLCT is only one of a multitude of other tumours encompassing DICER1 syndrome. The condition is inherited in an autosomal dominant fashion. As such, genetic counselling is a key component of the management of women with SLCT. |
format | Online Article Text |
id | pubmed-6176314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-61763142018-10-23 Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature Wormald, B. Elorbany, S. Hanson, H. Williams, J. W. Heenan, S. Barton, D. P. J. Case Rep Obstet Gynecol Case Report Sertoli-Leydig cell tumours of the ovary (SLCT) are rare tumours predominantly caused by mutations in the DICER1 gene. We present a patient with a unilateral SLCT who had an underlying germline DICER1 gene mutation. We discuss the underlying pathology, risks, and screening opportunities available to those with a mutation in this gene as SLCT is only one of a multitude of other tumours encompassing DICER1 syndrome. The condition is inherited in an autosomal dominant fashion. As such, genetic counselling is a key component of the management of women with SLCT. Hindawi 2018-09-25 /pmc/articles/PMC6176314/ /pubmed/30356399 http://dx.doi.org/10.1155/2018/7927362 Text en Copyright © 2018 B. Wormald et al. https://creativecommons.org/licenses/by/4.0/ 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 Wormald, B. Elorbany, S. Hanson, H. Williams, J. W. Heenan, S. Barton, D. P. J. Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature |
title | Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature |
title_full | Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature |
title_fullStr | Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature |
title_full_unstemmed | Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature |
title_short | Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature |
title_sort | sertoli-leydig cell tumour and dicer1 mutation: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176314/ https://www.ncbi.nlm.nih.gov/pubmed/30356399 http://dx.doi.org/10.1155/2018/7927362 |
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