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甲状腺激素抵抗最初被误诊为桥本甲状腺炎,诊断颇具挑战性。

Challenging diagnosis of thyroid hormone resistance initially as Hashimoto's thyroiditis.

作者信息

Ch'ng Tong Wooi, Chin Vivian L

机构信息

Department of Pediatrics, Division of Pediatric Endocrinology, SUNY Downstate Medical Center, Brooklyn, NY, USA.

出版信息

J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):203-206. doi: 10.1515/jpem-2018-0284.

Abstract

Background Resistance to thyroid hormone (RTH) commonly presents with goiter, attention deficit hyperactivity disorder (ADHD), short stature and tachycardia. However, due to its variable presentation with subtle clinical features, a third of the cases are mistreated, typically as hyperthyroidism. Case presentation A 15-year-old female with ADHD and oligomenorrhea was initially diagnosed as Hashimoto's thyroiditis but found to have a rare heterozygous mutation in c803 C>G (p Ala 268 Gly) in the THRβ gene, confirming resistance to thyroid hormone. Conclusions Fluctuating thyroid function tests in addition to thyroid peroxidase antibody (TPO Ab) positivity complicated the diagnosis of RTH, initially diagnosed as Hashimoto's thyroiditis. A high index of suspicion is needed to prevent misdiagnosis and mistreatment.

摘要

背景 甲状腺激素抵抗(RTH)通常表现为甲状腺肿大、注意力缺陷多动障碍(ADHD)、身材矮小和心动过速。然而,由于其临床表现多样且临床特征不明显,三分之一的病例被误诊,通常被误诊为甲状腺功能亢进症。病例报告 一名15岁患有ADHD和月经过少的女性最初被诊断为桥本甲状腺炎,但发现其THRβ基因存在罕见的c803 C>G(p Ala 268 Gly)杂合突变,确诊为甲状腺激素抵抗。结论 除甲状腺过氧化物酶抗体(TPO Ab)阳性外,甲状腺功能检查结果波动使RTH的诊断复杂化,最初被诊断为桥本甲状腺炎。需要高度怀疑指数以防止误诊和误治。

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