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Sexual precocity in a girl with early-onset Graves’ disease

We describe the case of a girl diagnosed with Graves’ disease (GD) at 2 yr of age, who developed early puberty. Preoperative examination for craniosynostosis revealed thyrotoxicosis. While she was tall and her bone age was advanced at GD onset, her linear growth attenuated after commencement of anti...

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Autores principales: Ogawa, Eishin, Isojima, Tsuyoshi, Sato, Yasuhiro, Motoyama, Kahoko, Kodama, Hiroko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073066/
https://www.ncbi.nlm.nih.gov/pubmed/30083033
http://dx.doi.org/10.1297/cpe.27.165
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author Ogawa, Eishin
Isojima, Tsuyoshi
Sato, Yasuhiro
Motoyama, Kahoko
Kodama, Hiroko
author_facet Ogawa, Eishin
Isojima, Tsuyoshi
Sato, Yasuhiro
Motoyama, Kahoko
Kodama, Hiroko
author_sort Ogawa, Eishin
collection PubMed
description We describe the case of a girl diagnosed with Graves’ disease (GD) at 2 yr of age, who developed early puberty. Preoperative examination for craniosynostosis revealed thyrotoxicosis. While she was tall and her bone age was advanced at GD onset, her linear growth attenuated after commencement of anti-thyroid treatment. However, at approximately 6 yr of age, breast budding was recognized. Hormonal analysis revealed pubertal levels of LH response to a GnRH stimulation test and serum E2. Gonadal suppression therapy with GnRH agonist was initiated, and her adult stature slightly exceeded the genetic potential. Although accelerated growth and skeletal maturation are often reported to occur at GD onset in prepubertal patients, early puberty is unusual, and this is the first reported case of sexual precocity in a girl with GD.
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spelling pubmed-60730662018-08-06 Sexual precocity in a girl with early-onset Graves’ disease Ogawa, Eishin Isojima, Tsuyoshi Sato, Yasuhiro Motoyama, Kahoko Kodama, Hiroko Clin Pediatr Endocrinol Case Report We describe the case of a girl diagnosed with Graves’ disease (GD) at 2 yr of age, who developed early puberty. Preoperative examination for craniosynostosis revealed thyrotoxicosis. While she was tall and her bone age was advanced at GD onset, her linear growth attenuated after commencement of anti-thyroid treatment. However, at approximately 6 yr of age, breast budding was recognized. Hormonal analysis revealed pubertal levels of LH response to a GnRH stimulation test and serum E2. Gonadal suppression therapy with GnRH agonist was initiated, and her adult stature slightly exceeded the genetic potential. Although accelerated growth and skeletal maturation are often reported to occur at GD onset in prepubertal patients, early puberty is unusual, and this is the first reported case of sexual precocity in a girl with GD. The Japanese Society for Pediatric Endocrinology 2018-07-31 2018 /pmc/articles/PMC6073066/ /pubmed/30083033 http://dx.doi.org/10.1297/cpe.27.165 Text en 2018©The Japanese Society for Pediatric Endocrinology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Ogawa, Eishin
Isojima, Tsuyoshi
Sato, Yasuhiro
Motoyama, Kahoko
Kodama, Hiroko
Sexual precocity in a girl with early-onset Graves’ disease
title Sexual precocity in a girl with early-onset Graves’ disease
title_full Sexual precocity in a girl with early-onset Graves’ disease
title_fullStr Sexual precocity in a girl with early-onset Graves’ disease
title_full_unstemmed Sexual precocity in a girl with early-onset Graves’ disease
title_short Sexual precocity in a girl with early-onset Graves’ disease
title_sort sexual precocity in a girl with early-onset graves’ disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073066/
https://www.ncbi.nlm.nih.gov/pubmed/30083033
http://dx.doi.org/10.1297/cpe.27.165
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