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颈部超声检查和核成像在先天性甲状腺功能减退症诊断中的作用

The Role of Neck Ultrasonography and Nuclear Imaging in the Diagnosis of Congenital Hypothyroidism.

作者信息

Sumathy Soundararajan, Palanivel Sengottaiyan, Nagaraju Kethipalli, Harisankar Chidambaram N B, Ashokraja Jeyaraj, Senthilkumar Jayachandran, Sreenivasan Palaniyappan, Sridhar Subbiah

机构信息

Department of Radiodiagnosis, Madurai Medical College and Govt. Rajaji Hospital, Madurai, Tamil Nadu, India.

Department of Endocrinology, Madurai Medical College and Govt. Rajaji Hospital, Madurai, Tamil Nadu, India.

出版信息

Indian J Endocrinol Metab. 2024 Nov-Dec;28(6):611-616. doi: 10.4103/ijem.ijem_7_24. Epub 2024 Dec 30.

Abstract

INTRODUCTION

Congenital hypothyroidism (CH) is the most common preventable cause of mental retardation, and the two important causes of CH are thyroid dysgenesis and dyshormonogenesis. Thyroid imaging is an integral part of identifying the specific aetiology of CH. We aimed to study the aetiological profile of CH and compare the imaging findings of ultrasonography (USG) and nuclear scintigraphy.

METHODS

It is a prospective, cross-sectional study conducted over 3 years. The clinical, USG, and technetium-99 (99 mTc) scintigraphy reports of CH children were analysed.

RESULTS

Sixty-two CH children were included in the study with an equal male-to-female ratio (1.1:1). There was a significant association between parental consanguinity and CH observed in 35.5% of cases ( = 0.006). In USG neck, 44 (71%) had normal and/or enlarged thyroid glands at the eutopic location, 16 (27.4%) cases had an absent gland, and ectopic as well as hypoplastic unilateral gland was observed in one (1.6%) each. Among 35 children, who underwent scintigraphy, 12 (34.3%) had absent uptake, 4 (11.4%) had ectopic uptake, and 1 (2.8%) child had unilateral normal uptake. The remaining 18 (51.5%) children, whose scintigraphy showed normal or avid uptakes, were diagnosed with dyshormonogenesis. Three cases were diagnosed as apparent athyreosis.

CONCLUSION

Dyshormonogeneis is the more commonly observed etiology of CH as compared to thyroid agenesis in the present study. A combined imaging approach with scintigraphy and USG is needed to delineate the specific etiology of CH. We need long-term Indian data to know the paradigm shift in the etiological pattern of CH as compared to Western studies.

摘要

引言

先天性甲状腺功能减退症(CH)是智力发育迟缓最常见的可预防病因,CH的两个重要病因是甲状腺发育不全和激素合成障碍。甲状腺成像对于确定CH的具体病因至关重要。我们旨在研究CH的病因谱,并比较超声检查(USG)和核素闪烁扫描的影像学表现。

方法

这是一项为期3年的前瞻性横断面研究。分析了CH患儿的临床、USG和锝-99(99mTc)闪烁扫描报告。

结果

62名CH患儿纳入研究,男女比例相等(1.1:1)。35.5%的病例中观察到近亲结婚与CH之间存在显著关联(P = 0.006)。在USG颈部检查中,44例(71%)在正常位置甲状腺正常和/或肿大,16例(27.4%)甲状腺缺如,1例(1.6%)为异位甲状腺以及1例(1.6%)为单侧甲状腺发育不全。在35例接受闪烁扫描的患儿中,12例(34.3%)摄取缺如,4例(11.4%)有异位摄取,1例(2.8%)患儿单侧摄取正常。其余18例(51.5%)闪烁扫描显示正常或摄取活跃的患儿被诊断为激素合成障碍。3例被诊断为明显的无甲状腺症。

结论

在本研究中,与甲状腺发育不全相比,激素合成障碍是CH更常见的病因。需要结合闪烁扫描和USG的成像方法来确定CH的具体病因。与西方研究相比,我们需要长期的印度数据来了解CH病因模式的转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a420/11774417/5194226898a8/IJEM-28-611-g001.jpg

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