被诊断为桥本氏甲状腺炎的儿童和青少年的流行病学、临床、实验室和放射学特征:单中心经验

IF 1.3 Q3 PEDIATRICS Turkish archives of pediatrics Pub Date : 2024-11-01 DOI:10.5152/TurkArchPediatr.2024.24174
Fatih Kilci, Emre Sarıkaya
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引用次数: 0

摘要

研究目的本研究旨在调查被诊断为桥本氏甲状腺炎的儿童的流行病学、临床、实验室和放射学特征,并介绍一家转诊中心的经验:本研究纳入了2020年1月至2024年5月期间在一家中心确诊为桥本氏甲状腺炎的200名儿童患者。数据从参与者的病历中提取并整理,包括临床信息、体格检查结果、实验室检查结果和放射影像学检查结果:研究对象确诊时的平均年龄为(11.3 ± 3.2)岁,女性居多。临床表现时,8.5%的研究对象年龄在 6 岁或以下。大多数患者(占总数的 39.5%)的甲状腺功能正常。此外,33.5%的患者被归类为亚临床甲状腺功能减退症,22%的患者表现为明显的甲状腺功能减退症,5%的患者表现为甲状腺功能亢进症。约有三分之一的研究参与者因在常规筛查中发现甲状腺功能检测结果异常而被转诊接受进一步评估。48%的患者有甲状腺疾病家族史。确诊时,39.5%的患者处于青春期前。与青春期患者相比,青春期前患者的明显甲状腺机能减退率更高(41.8% 对 9.1%,P < .005)。平均腺体体积SDS为2.61 ± 3.69,45.5%的患者患有甲状腺肿。5.5%的研究参与者发现了甲状腺结节病变。对5名患者进行了细针穿刺活检,其中3例为良性,其余2例为意义不明的不典型性:结论:亚临床甲状腺功能减退症患者初次发病时的基线 TSH 水平超过 8.5 mIU/L,如果不接受治疗,很可能在随后的随访中发展为明显的甲状腺功能减退症。与之前的报告相比,青春期前的病例更常见,青春期前患者的甲减病程也更严重。这些研究结果表明,儿童自身免疫病的发病时间可能会提前。为了证实这一观察结果,还需要进一步的研究。
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Epidemiological, Clinical, Laboratory, and Radiological Characteristics of Children and Adolescents Diagnosed with Hashimoto's Thyroiditis: A Single-Center Experience.

Objective: This study aimed to investigate the epidemiological, clinical, laboratory, and radiological characteristics of children diagnosed with Hashimoto's thyroiditis and to present the experiences of a referral center.

Materials and methods: This study included 200 pediatric patients diagnosed with Hashimoto's thyroiditis between January 2020 and May 2024 at a single center. The data were extracted and compiled from the participants' medical records, including clinical information, physical examination findings, laboratory test results, and radiological imaging.

Results: Mean age of the study population was 11.3 ± 3.2 years at diagnosis, with a female predominance. At the time of clinical presentation, 8.5% of the study participants were 6 years of age or younger. The majority of patients, comprising 39.5% of the cohort, exhibited euthyroid thyroid function. Additionally, 33.5% of the patients were classified as having subclinical hypothyroidism, 22% demonstrated overt hypothyroidism, and 5% presented with hyperthyroidism. Approximately one-third of the study participants were referred for further evaluation due to the identification of abnormal thyroid function test results during routine screening examinations. 48% of the patients had a documented family history of thyroid disease. At diagnosis, 39.5% were prepubertal. The rate of overt hypothyroidism was higher in prepubertal patients compared to pubertal patients (41.8% vs. 9.1%, P < .005). Mean gland volume SDS was 2.61 ± 3.69, and 45.5% had goiter. Thyroid nodular lesions were identified in 5.5% of the study participants. Fine-needle aspiration biopsy was performed on five patients, revealing benign findings in three cases and atypia of undetermined significance in the remaining two cases.

Conclusion: Patints with subclinical hypothyroidism who have a baseline TSH level exceeding 8.5 mIU/L at initial presentation and do not receive treatment are likely to progress to overt hypothyroidism during subsequent follow-up. Prepubertal cases were more frequently observed compared to previous reports, and the course of hypothyroidism was more severe in prepubertal patients. These findings suggest a potential shift towards earlier onset of autoimmunity in children. Further studies are warranted to substantiate this observation.

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