Literature DB >> 23006743

Thyroid abnormalities in children and adolescents with McCune-Albright syndrome.

D Tessaris1, A Corrias, P Matarazzo, L De Sanctis, M Wasniewska, M F Messina, M C Vigone, R Lala.   

Abstract

BACKGROUND: To date, there is no agreement about the frequency or the features of thyroid abnormalities in McCune-Albright syndrome (MAS). The aim of our study was to detect thyroid abnormalities in a cohort of MAS children and adolescents and to give indications for their treatment and follow-up.
METHODS: In 36 patients, 22 females and 14 males, thyroid function and sonographic features of thyroid were evaluated every 6-12 months.
RESULTS: Three males and 1 female had hyperthyroidism: 2 with nodular, 2 with diffuse goiters. They were treated with methimazole (0.2-0.5 mg/kg/day) with good clinical and biochemical responses. The remaining 32 patients were euthyroid, even if 7 displayed sonographic alterations, of whom 5 had nodular goiter with nodules >1 cm, and 2 micronodular goiter. Fine-needle aspiration biopsy was performed in 2 patients with nodules >1 cm, 1 showing hemorrhagic nodule and 1 colloid cystic nodule.
CONCLUSIONS: Prevalence of thyroid alterations in the studied MAS series was 31%. 64% of 11 patients with thyroid alterations had nodular goiters, with nodules >1 cm. As the onset of thyroid disease ranged from 1 to 20 years, a strict monitoring of thyroid function is recommended every 6 months. Satisfactory treatment can be obtained and maintained with antithyroid drugs.
Copyright © 2012 S. Karger AG, Basel.

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Year:  2012        PMID: 23006743     DOI: 10.1159/000342641

Source DB:  PubMed          Journal:  Horm Res Paediatr        ISSN: 1663-2818            Impact factor:   2.852


  15 in total

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Authors:  Cemre Robinson; Michael T Collins; Alison M Boyce
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Review 2.  Fibrous Dysplasia of Bone and McCune-Albright Syndrome: A Bench to Bedside Review.

Authors:  Iris Hartley; Maria Zhadina; Micheal T Collins; Alison M Boyce
Journal:  Calcif Tissue Int       Date:  2019-04-29       Impact factor: 4.333

Review 3.  DIAGNOSIS OF ENDOCRINE DISEASE: Mosaic disorders of FGF23 excess: Fibrous dysplasia/McCune-Albright syndrome and cutaneous skeletal hypophosphatemia syndrome.

Authors:  Luis F de Castro; Diana Ovejero; Alison M Boyce
Journal:  Eur J Endocrinol       Date:  2020-05       Impact factor: 6.664

Review 4.  The Clinical Spectrum of McCune-Albright Syndrome and Its Management.

Authors:  Tiahna Spencer; Kristen S Pan; Michael T Collins; Alison M Boyce
Journal:  Horm Res Paediatr       Date:  2019-12-19       Impact factor: 2.852

5.  Genotype-Phenotype Correlation in Fibrous Dysplasia/McCune-Albright Syndrome.

Authors:  Maria Zhadina; Kelly L Roszko; Raya E S Geels; Luis F de Castro; Michael T Collins; Alison M Boyce
Journal:  J Clin Endocrinol Metab       Date:  2021-04-23       Impact factor: 5.958

6.  Rare thyroid non-neoplastic diseases.

Authors:  Katarzyna Lacka; Adam Maciejewski
Journal:  Thyroid Res       Date:  2015-04-11

7.  Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study.

Authors:  Eun-Kyung Cho; Jinsup Kim; Aram Yang; Chang-Seok Ki; Ji-Eun Lee; Sung Yoon Cho; Dong-Kyu Jin
Journal:  Orphanet J Rare Dis       Date:  2016-08-09       Impact factor: 4.123

Review 8.  Auxological and Endocrinological Features in Children With McCune Albright Syndrome: A Review.

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Journal:  Front Endocrinol (Lausanne)       Date:  2020-08-04       Impact factor: 5.555

Review 9.  Fibrous dysplasia for radiologists: beyond ground glass bone matrix.

Authors:  Yevgeniya S Kushchayeva; Sergiy V Kushchayev; Tetiana Y Glushko; Sri Harsha Tella; Oleg M Teytelboym; Michael T Collins; Alison M Boyce
Journal:  Insights Imaging       Date:  2018-11-27

Review 10.  Fibrous Dysplasia/McCune-Albright Syndrome: A Rare, Mosaic Disease of Gα s Activation.

Authors:  Alison M Boyce; Michael T Collins
Journal:  Endocr Rev       Date:  2020-04-01       Impact factor: 19.871

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