Case Reports in Obstetrics and Gynecology (Jan 2018)

Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature

  • B. Wormald,
  • S. Elorbany,
  • H. Hanson,
  • J. W. Williams,
  • S. Heenan,
  • D. P. J. Barton

DOI
https://doi.org/10.1155/2018/7927362
Journal volume & issue
Vol. 2018

Abstract

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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.