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This article is protected by copyright. All rights reserved.AIMS Sertoli-Leydig cell tumours (SLCT) are rare ovarian neoplasms commonly associated with somatic or germline DICER1 mutations, especially when of moderately or poorly differentiated type. A large majority are unilateral but bilateral neoplasms have been reported, sometimes in the context of germline DICER1 mutations (DICER1 syndrome). It is currently unknown whether these represent independent neoplasms or metastasis from one ovary to the other. METHODS AND RESULTS We report 3
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