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先天性甲状腺功能减退症患儿异位甲状腺组织的超声评估

Ultrasonographic assessment of the ectopic thyroid tissue in children with congenital hypothyroidism.

作者信息

Marinovic Daniela, Garel Catherine, Czernichow Paul, Léger Juliane

机构信息

Paediatric Endocrinology Unit and INSERM U457, Hôpital Robert Debré, Boulevard Serrurier 48, 75019 Paris Cedex 19, France.

出版信息

Pediatr Radiol. 2004 Feb;34(2):109-13. doi: 10.1007/s00247-003-1043-1. Epub 2003 Oct 28.

Abstract

BACKGROUND

Ectopic thyroid tissue as a result of thyroid developmental abnormalities is the most frequent cause of congenital hypothyroidism (CH). It is diagnosed by using radionuclide thyroid scanning. OBJECTIVE. To evaluate the sensitivity of US in the detection of such ectopias and to describe their US pattern before and during treatment.

MATERIALS AND METHODS

Forty-two neonates (group A; aged 11.3+/-4.0 days) and 33 older children (group B; aged 11.1+/-3.9 years) with a biochemical diagnosis of CH and thyroid ectopia detected by radionuclide scanning were evaluated before (group A) and after (group B) treatment. Thyroid US included a survey of the pathway of the thyroglossal tract and an evaluation of the location, size, echogenicity and vascularity of any tissue along this pathway suggestive of thyroid ectopia.

RESULTS

Thyroid ectopia was detected using US in 18 patients (24%) with a similar rate during the neonatal period and thereafter on therapy. Three patients demonstrated double ectopia. These 21 sites of ectopic thyroid tissue were located at the suprahyoid level (n=12), at the level of the hyoid (n=1), and at the infrahyoid level (n=8). The maximum diameter of the ectopic tissue ranged from 4 to 14 mm. In group A (9 patients), the 11 ectopias were all hypervascular. These were hyperechoic in all but one neonate. In group B (9 patients), the ten ectopias were not vascular, and were hyper (n=3) or hypoechoic (n=7).

CONCLUSIONS

US allows for detection of ectopic thyroid tissue, but with a lower detection rate than radionuclide scanning. However, it does provide a more detailed description of such ectopias.

摘要

背景

甲状腺发育异常导致的异位甲状腺组织是先天性甲状腺功能减退症(CH)最常见的病因。通过放射性核素甲状腺扫描进行诊断。目的:评估超声检测此类异位甲状腺的敏感性,并描述其在治疗前和治疗期间的超声表现。

材料与方法

对42例新生儿(A组;年龄11.3±4.0天)和33例年龄较大儿童(B组;年龄11.1±3.9岁)进行评估,这些患儿经生化诊断为CH且经放射性核素扫描检测出甲状腺异位。在治疗前(A组)和治疗后(B组)对其进行甲状腺超声检查。甲状腺超声检查包括对甲状舌管走行的探查以及对沿此路径提示甲状腺异位的任何组织的位置、大小、回声和血管情况的评估。

结果

超声检测出18例患者存在甲状腺异位(24%),新生儿期及治疗后的检出率相似。3例患者表现为双重异位。这21个异位甲状腺组织部位位于舌骨上水平(n = 12)、舌骨水平(n = 1)和舌骨下水平(n = 8)。异位组织的最大直径为4至14毫米。在A组(9例患者)中,11个异位甲状腺均为高血管性。除1例新生儿外,其余均为高回声。在B组(9例患者)中,10个异位甲状腺无血管,其中3个为高回声,7个为低回声。

结论

超声能够检测出异位甲状腺组织,但检出率低于放射性核素扫描。然而,它确实能更详细地描述此类异位甲状腺。

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