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印度一家三级护理医院中的甲状腺激素合成障碍及相关非甲状腺异常。

Thyroid dyshormonogenesis and associated non-thyroidal anomalies in a tertiary care hospital in India.

作者信息

Rather Tanveer A, Khan Shoukat H, Masoodi Shariq, Alai Mohd Sultan

机构信息

Department of Nuclear Medicine, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.

出版信息

Horm Res Paediatr. 2014;81(5):314-8. doi: 10.1159/000357843. Epub 2014 Mar 14.

Abstract

BACKGROUND

Dyshormonogenetic goiter refers to familial goiters owing to an inherited defect in the metabolism of thyroid hormones.

METHODS

19 patients with clinical and biochemically proven hypothyroidism (low T3, FT4 and high TSH) were recruited for the study. All patients were subjected to (i) ultrasound of the neck to rule out thyroid dysgenesis and (ii) technetium-99m radionuclide thyroid scintigraphy and a perchlorate discharge test (PDT). Extrathyroidal malformations were identified by clinical ultrasound (USG) examination of the abdomen and pelvis and by echocardiography.

RESULTS

Out of 19 patients with elevated thyroid uptakes on technetium-99m thyroid scintigraphy, 12 (63%) had a positive PDT and 7 patients (37%) had a negative PDT. All patients were subjected to abdominopelvic USG and echocardiography. Out of 12 patients with a positive PDT, 5 (42%) had associated extrathyroid malformations, 2 had urogenital malformations, and cardiac abnormalities on echocardiography were present in 2 patients (17%). One patient (8%) had features of dysmorphism in the form of a high-arched palate, low-set ears and microcephaly.

CONCLUSION

Congenital hypothyroidism due to dyshormogenesis is associated with a high prevalence of extrathyroidal malformations and needs to be managed as early as possible to ensure normal neurocognitive development of the children affected.

摘要

背景

激素合成障碍性甲状腺肿是指由于甲状腺激素代谢的遗传缺陷导致的家族性甲状腺肿。

方法

招募了19例临床及生化检查证实为甲状腺功能减退(T3、游离甲状腺素降低,促甲状腺激素升高)的患者进行研究。所有患者均接受了以下检查:(i)颈部超声检查以排除甲状腺发育不全;(ii)99m锝放射性核素甲状腺闪烁显像及过氯酸盐释放试验(PDT)。通过腹部和骨盆的临床超声(USG)检查及超声心动图检查来识别甲状腺外畸形。

结果

在99m锝甲状腺闪烁显像显示甲状腺摄取率升高的19例患者中,12例(63%)PDT结果为阳性,7例(37%)PDT结果为阴性。所有患者均接受了腹部盆腔USG检查及超声心动图检查。在12例PDT结果为阳性的患者中,5例(42%)伴有甲状腺外畸形,2例有泌尿生殖系统畸形,2例(17%)超声心动图显示有心脏异常。1例患者(8%)有高拱腭、低位耳和小头畸形等畸形特征。

结论

激素合成障碍所致的先天性甲状腺功能减退与甲状腺外畸形的高发生率相关,需要尽早进行管理以确保受影响儿童的神经认知正常发育。

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