{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,28]],"date-time":"2026-07-28T20:21:53Z","timestamp":1785270113170,"version":"3.55.0"},"reference-count":15,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2018,9,25]],"date-time":"2018-09-25T00:00:00Z","timestamp":1537833600000},"content-version":"vor","delay-in-days":267,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Case Reports in Obstetrics and Gynecology"],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:p>\n                    Sertoli\u2010Leydig cell tumours of the ovary (SLCT) are rare tumours predominantly caused by mutations in the\n                    <jats:italic>DICER1<\/jats:italic>\n                    gene. We present a patient with a unilateral SLCT who had an underlying germline\n                    <jats:italic>DICER1<\/jats:italic>\n                    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\n                    <jats:italic>DICER1<\/jats:italic>\n                    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.\n                  <\/jats:p>","DOI":"10.1155\/2018\/7927362","type":"journal-article","created":{"date-parts":[[2018,9,25]],"date-time":"2018-09-25T19:33:45Z","timestamp":1537904025000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Sertoli\u2010Leydig Cell Tumour and\n                    <i>DICER1<\/i>\n                    Mutation: A Case Report and Review of the Literature"],"prefix":"10.1155","volume":"2018","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6464-5391","authenticated-orcid":false,"given":"B.","family":"Wormald","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S.","family":"Elorbany","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H.","family":"Hanson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J. 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