Hyperthyroidism in McCune-Albright Syndrome - a case report.
McCune-albright syndrome
hyperfunctioning endocrinopathies
hyperthyroidism
polyostotic fibrous dysplasia
Journal
Journal of pediatric endocrinology & metabolism : JPEM
ISSN: 2191-0251
Titre abrégé: J Pediatr Endocrinol Metab
Pays: Germany
ID NLM: 9508900
Informations de publication
Date de publication:
28 Mar 2023
28 Mar 2023
Historique:
received:
14
07
2022
accepted:
24
10
2022
pubmed:
10
11
2022
medline:
8
3
2023
entrez:
9
11
2022
Statut:
epublish
Résumé
We intend to describe a case of McCune-Albright Syndrome (MAS), a rare disease characterized by fibrous dysplasia (FD), cutaneous hyperpigmentation and hyperfunctioning endocrinopathies (HFE). We report the case of a 13-year-old male child who presented with a This is a case of MAS-associated HT that reflects the deleterious effect of thyroid hormone excess on FD, reinforcing the need of having a low threshold for suspicion of HFE that may arise.
Identifiants
pubmed: 36351197
pii: jpem-2022-0357
doi: 10.1515/jpem-2022-0357
doi:
Substances chimiques
Hormones
0
Diphosphonates
0
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
Pagination
319-322Informations de copyright
© 2022 Walter de Gruyter GmbH, Berlin/Boston.
Références
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Tessaris, D, Corrias, A, Matarazzo, P, De Sanctis, L, Wasniewska, M, Messina, MF, et al.. Thyroid abnormalities in children and adolescents with McCune-Albright Syndrome. Horm Res Paediatr 2012;78:151–7. https://doi.org/10.1159/000342641 .
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doi: 10.1159/000504802
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doi: 10.1177/2333794X19875153
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doi: 10.1590/s0004-27302008000300017
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doi: 10.1002/jbmr.4463