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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...

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Detalles Bibliográficos
Autores principales: Wormald, B., Elorbany, S., Hanson, H., Williams, J. W., Heenan, S., Barton, D. P. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
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.
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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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