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一过性先天性甲状腺功能减退症与甲状腺刺激素受体阻断抗体相关:病例系列研究。

Transient congenital hypothyroidism due to thyroid-stimulating hormone receptor blocking antibodies: a case series.

机构信息

Department of Medical Biochemistry and Immunology, University Hospital of Wales, Cardiff, UK.

出版信息

Ann Clin Biochem. 2011 Jul;48(Pt 4):386-90. doi: 10.1258/acb.2011.011007. Epub 2011 May 23.

Abstract

We describe seven infants with transient congenital hypothyroidism (CH) due to maternal thyroid-stimulating hormone receptor (TSH-R) blocking antibodies (TRAb) identified over three decades of newborn screening for CH in Wales, UK that represents a minimum incidence of 1.6% of CH cases. Infants with transient CH due to maternal TRAb presented with a spectrum of clinical and biochemical hypothyroidism. Blood spot TSH concentrations ranged 60.5-332 mIU/L. CH was confirmed by plasma thyroid function tests in all cases (plasma TSH ranged 21-752 mIU/L). The seven infants belonged to five different families. On examination, four infants were clinically hypothyroid. Five infants had a thyroid ultrasound, of which three were abnormal. All infants were treated with thyroxine, which was subsequently withdrawn from three. Following thyroxine withdrawal, one infant resumed normal thyroid function and two developed compensated hypothyroidism. Of the five mothers, two had undiagnosed hypothyroidism and three were receiving thyroxine for longstanding hypothyroidism. Thyroid peroxidase antibody (aTPO) was measured in four and was negative in two, borderline positive in one and strongly positive in another. TRAb was measured in all five women and was strongly positive in all of them. This case series highlights the importance of identifying CH due to TRAb by investigating both the infant and the mother following a raised TSH found on newborn screening. The identification of those infants with transient CH caused by maternal transfer of TRAb is essential for optimizing management during childhood (including potential withdrawal of thyroxine replacement in the longer term) and in any subsequent pregnancy.

摘要

我们描述了在英国威尔士进行新生儿筛查的三十多年中发现的 7 例因母体甲状腺刺激素受体(TSH-R)阻断抗体(TRAb)导致的短暂性先天性甲状腺功能减退症(CH)的婴儿。这些病例的发生率至少为 1.6%。由于母体 TRAb 导致的短暂性 CH 的婴儿表现为一系列临床和生化甲状腺功能减退的症状。血斑 TSH 浓度范围为 60.5-332mIU/L。所有病例均通过血浆甲状腺功能检查证实存在 CH(血浆 TSH 范围为 21-752mIU/L)。这 7 名婴儿分属于 5 个不同的家庭。检查时,4 名婴儿存在临床甲状腺功能减退。5 名婴儿进行了甲状腺超声检查,其中 3 名异常。所有婴儿均接受了甲状腺素治疗,其中 3 名随后停药。停药后,1 名婴儿恢复了正常甲状腺功能,2 名婴儿发展为代偿性甲状腺功能减退。5 名母亲中,2 名患有未确诊的甲状腺功能减退,3 名因长期甲状腺功能减退而正在接受甲状腺素治疗。4 名母亲检测了甲状腺过氧化物酶抗体(aTPO),其中 2 名阴性,1 名弱阳性,1 名强阳性。所有 5 名女性均检测了 TRAb,均呈强阳性。本病例系列强调了在新生儿筛查发现 TSH 升高后,通过对婴儿和母亲进行调查,识别因 TRAb 引起的 CH 的重要性。对于识别因母体转移的 TRAb 导致的短暂性 CH 的婴儿至关重要,这有助于优化儿童期的管理(包括在长期内潜在停止甲状腺素替代治疗)以及任何后续妊娠。

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