新生儿筛查未发现甲状腺异位所致的先天性甲状腺功能减退- 1例报告。

Q3 Medicine
Anna Stępniewska, Małgorzata Wójcik, Jerzy B Starzyk
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引用次数: 0

摘要

新生儿筛查先天性甲状腺功能减退症(CH)已经非常有效地预防破坏性的神经发育和身体后遗症的影响婴儿。我们报告一例在3个月大时发现的位于下颌骨区域的异位甲状腺,在基于两次重复的干血点TSH测量的先天性甲状腺功能减退筛查试验中被遗漏。经内分泌门诊血液检查,确认诊断为亚临床甲状腺功能减退:TSH 26.3µIU/ml (N:
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Congenital hypothyroidism due to thyroid ectopy not detected in neonatal screening - case report.

Congenital hypothyroidism due to thyroid ectopy not detected in neonatal screening - case report.

Congenital hypothyroidism due to thyroid ectopy not detected in neonatal screening - case report.

Newborn screening for congenital hypothyroidism (CH) has been highly effective in preventing devastating neurodevelopmental and physical sequelae in affected infants. We report a case of an ectopic thyroid gland located in the submandibular area detected at the age of 3 months, which was missed by congenital hypothyroidism screening test based on twice-repeated TSH measurement in dried blood spots. The diagnosis of subclinical hypothyroidism was confirmed on the basis of blood test performed in the endocrine clinic: TSH 26.3 µIU/ml (N: < 10 µIU/ml), with FT4 14.7 pmol/l (N: 10-25 pmol/l) and fT3 6.9 pmol/l (N: 3-8 pmol/l). Ultrasonography and scintigraphy revealed ectopically located thyroid tissue in the sublingual area. In the case of doubtful results of a neonatal screening test or in any case of suspected congenital hypothyroidism, the diagnosis should be supplemented with ultrasound examination of the neonate's neck and followed by scintigraphy if necessary.

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来源期刊
Pediatric Endocrinology, Diabetes and Metabolism
Pediatric Endocrinology, Diabetes and Metabolism Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.00
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发文量
36
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