Journal of Pediatric Surgery Case Reports (Aug 2016)

DICER1 syndrome and thyroid disease

  • Michael Canfarotta,
  • Rebecca Riba-Wolman,
  • Andrea D. Orsey,
  • Fabiola Balarezo,
  • Christine Finck

DOI
https://doi.org/10.1016/j.epsc.2016.05.014
Journal volume & issue
Vol. 11, no. C
pp. 31 – 34

Abstract

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DICER1, a member of the ribonuclease III (RNase III) family, is known to play an important role in the post-transcriptional regulation of gene expression and germline mutations have been associated with a familial tumor susceptibility syndrome. In this report, we describe an 11-year-old female with a history of ovarian Sertoli-Leydig cell tumor resection and known DICER1 mutation (c.325C>T, p.Gln109*). She presented with multiple thyroid nodules on screening ultrasound. On fine needle aspiration she was found to have cytologic atypia, which in the general adult population confers a 5–15% risk of malignancy. Herein, we review the literature on DICER1 phenotype and pediatric thyroid disease and discuss management options.

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