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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Veröffentlicht in: | Case reports in obstetrics and gynecology 2018, Vol.2018 (2018), p.1-4 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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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ISSN: | 2090-6684 2090-6692 |
DOI: | 10.1155/2018/7927362 |