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特纳综合征中的桥本氏病。

Hashimoto's disease in Turner's syndrome.

作者信息

Fleming S, Cowell C, Bailey J, Burrow G N

机构信息

Toronto General Hospital, Ontario, Canada

出版信息

Clin Invest Med. 1988 Aug;11(4):243-6.

PMID:3168347
Abstract

Sera from 52 patients with Turner's syndrome were analyzed for thyroxine and TSH concentrations, resin T3 uptake, and thyroid antibodies. Thyroid antibody titers were compared to those previously obtained in 53 women with long-standing infertility. Thyroid microsomal and/or thyroglobulin antibody titers were elevated to a level diagnostic of Hashimoto's disease (greater than 1:400) in 25 (48%) patients with Turner's syndrome. Microsomal antibody levels only were elevated in five (9%) patients with infertility. The mean microsomal antibody titers in the patients with Turner's syndrome (1:25, 167 +/- 31,531) were significantly higher than in the infertile patients (1:2560 +/- 2149). The incidence of Hashimoto's disease did not differ significantly among the various karyotypes. The entire clinical spectrum of Hashimoto's thyroiditis was present in Turner's syndrome. Three patients had overt hypothyroidism necessitating L-thyroxine, four had compensated hypothyroidism (serum TSH concentration greater than 10 microU/L and normal serum thyroxine concentrations), while the remaining 18 had normal thyroid function. No relationship was demonstrated between Hashimoto's disease or family history of thyroid disease and karyotype.

摘要

对52例特纳综合征患者的血清进行了甲状腺素、促甲状腺激素(TSH)浓度、树脂T3摄取率及甲状腺抗体分析。将甲状腺抗体滴度与之前在53例长期不孕女性中测得的结果进行比较。25例(48%)特纳综合征患者的甲状腺微粒体和/或甲状腺球蛋白抗体滴度升高至诊断桥本氏病的水平(大于1:400)。仅5例(9%)不孕患者的微粒体抗体水平升高。特纳综合征患者的平均微粒体抗体滴度(1:25,167±31,531)显著高于不孕患者(1:2560±2149)。桥本氏病的发病率在不同核型之间无显著差异。特纳综合征患者中存在桥本氏甲状腺炎的全部临床谱。3例患者出现明显甲状腺功能减退,需要服用左甲状腺素;4例患者为代偿性甲状腺功能减退(血清TSH浓度大于10 μU/L且血清甲状腺素浓度正常),其余18例甲状腺功能正常。未发现桥本氏病或甲状腺疾病家族史与核型之间存在关联。

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