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Journal of Korean Medical Science ; : 1368-1371, 2010.
Artigo em Inglês | WPRIM | ID: wpr-187903

RESUMO

Resistance to thyroid hormone (RTH) is an autosomal dominant hereditary disorder that is difficult to diagnose because of its rarity and variable clinical features. The magnitude of RTH is caused by mutations in the thyroid hormone receptor beta (TRbeta) gene. We recently treated a 38-yr-old woman with RTH who had incidental papillary thyroid carcinoma. She presented with goiter and displayed elevated thyroid hormone levels with an unsuppressed TSH. She was determined to harbor a missense mutation of M310T in exon 9 of the TRbeta gene, and diagnosed with generalized RTH. This mutation has not yet been reported in Korea. RTH is very rare and easily overlooked, but should be considered in patients who present with goiter and elevated thyroid hormone levels with an unsuppressed TSH. The association between thyroid cancer and RTH needs further study.


Assuntos
Adulto , Feminino , Humanos , Diagnóstico Diferencial , Éxons , Mutação de Sentido Incorreto , Glândula Tireoide/diagnóstico por imagem , Receptores beta dos Hormônios Tireóideos/genética , Síndrome da Resistência aos Hormônios Tireóideos/complicações , Hormônios Tireóideos/sangue , Neoplasias da Glândula Tireoide/complicações
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