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甲状腺超声和血清降钙素对先天性甲状腺功能减退症诊断的贡献。

Contribution of thyroid ultrasound and serum calcitonin to the diagnosis of congenital hypothyroidism.

作者信息

Chanoine J P, Toppet V, Body J J, Van Vliet G, Lagasse R, Bourdoux P, Spehl M, Delange F

机构信息

Department of Pediatrics, Hospital Saint-Pierre, Bruxelles, Belgium.

出版信息

J Endocrinol Invest. 1990 Feb;13(2):103-9. doi: 10.1007/BF03349517.

DOI:10.1007/BF03349517
PMID:2184189
Abstract

UNLABELLED

To elucidate the role of thyroid ultrasound (TU) in the diagnosis of congenital hypothyroidism (CH), we compared 1) TU and thyroid scintigraphy (TS) in 6 CH newborns and 2) TU results in the 6 CH newborns, in 8 newborns with "false positive" results at screening, in 13 CH children aged 2 mo to 12 yr treated since the neonatal period and in 235 controls aged 0-12 yr.

RESULTS

  1. In all 6 CH newborns with no thyroid uptake at TS, TU evidenced small posterior hyperechogenic masses in the thyroid area [Vol: 322 +/- 180 (SD) mm3]; 2) In all normal controls and in the 8 "false positive" cases at screening TU showed normal thyroid structures. The thyroid volume was 831 +/- 383 mm3 in normal newborns and progressively increased with age. In the older CH children, TU also demonstrated the hyperechogenic masses, but their volume barely increased with age: as a consequence, the difference between the volume of the masses in CH patients and the thyroid tissue in controls, already significant in newborns (p less than 0.01), markedly increased with age. The exact nature of these masses is unknown; they could represent poorly vascularized ultimobranchial remnants containing the calcitonin - secreting cells: this hypothesis is supported by our finding that serum concentrations of calcitonin (measured by a sensitive extraction method) (mean +/- SD, pg/ml) were lower in the CH patients (2.9 +/- 1.5) than in controls (13.0 +/- 6.9; p less than 0.001) at birth. In conclusion, in all cases of CH, TU showed abnormal structures in the thyroid area. TU and TS provide complementary information in the diagnosis of CH, and TU should be routinely performed in all newborns suspected of CH to avoid unnecessary use of TS in unaffected infants.
摘要

未标注

为阐明甲状腺超声(TU)在先天性甲状腺功能减退症(CH)诊断中的作用,我们比较了:1)6例CH新生儿的TU和甲状腺闪烁显像(TS);2)6例CH新生儿、8例筛查结果为“假阳性”的新生儿、13例自新生儿期起接受治疗的2个月至12岁的CH儿童以及235例0至12岁对照儿童的TU结果。

结果

1)在所有6例TS显示无甲状腺摄取的CH新生儿中,TU显示甲状腺区域有小的后方高回声团块[体积:322±180(标准差)mm³];2)在所有正常对照以及8例筛查“假阳性”病例中,TU显示甲状腺结构正常。正常新生儿的甲状腺体积为831±383mm³,并随年龄逐渐增加。在年龄较大的CH儿童中,TU也显示出高回声团块,但其体积几乎不随年龄增加:因此,CH患者团块体积与对照甲状腺组织体积之间的差异在新生儿中已很显著(p<0.01),并随年龄显著增加。这些团块的确切性质尚不清楚;它们可能代表血管化不良的终末鳃体残余物,其中含有分泌降钙素的细胞:这一假设得到了我们的发现的支持,即出生时CH患者血清降钙素浓度(通过敏感提取法测量)(平均值±标准差,pg/ml)低于对照(13.0±6.9;p<0.001)。总之,在所有CH病例中,TU显示甲状腺区域结构异常。TU和TS在CH诊断中提供互补信息,对于所有疑似CH的新生儿应常规进行TU检查,以避免在未受影响的婴儿中不必要地使用TS。

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Calcitonin secretion in congenital nongoitrous cretinism.先天性非甲状腺肿型克汀病中的降钙素分泌
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