[儿童原发性甲状旁腺功能亢进症]。

A R Benina, A A Kolodkina, A N Tiul'pakov, N Yu Kalinchenko, D M Brovin, A V Anikiev, O S Danilenko, M S Sheremeta, V V Zakharova, E N Solodovnikova, O B Bezlepkina
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引用次数: 0

摘要

背景: 原发性甲状旁腺功能亢进症(PHPT)是一种内分泌疾病,其特点是由于原发性甲状腺病变导致甲状旁腺激素(PTH)分泌过多,血钙水平高于正常或升高。PHPT在儿童中是一种罕见的病变,根据文献报道,其发病率为2-5:100,000。由于发病时临床表现(恶心、呕吐、腹痛、情绪不稳定)的非特异性,该病可能长期得不到诊断。目的:研究儿童原发性甲状旁腺功能亢进症的病程特点和分子遗传学基础: 对49名确诊为原发性甲状旁腺功能亢进症的患者进行回顾性观察研究。所有患者均于2014-2022年间在俄罗斯内分泌学研究中心儿科内分泌学研究所接受了全面的实验室仪器和分子遗传学研究: 首次出现PHPT临床症状的年龄为13.8岁[10.6;1 5.2],其中以疲劳、头痛、消化不良、下肢疼痛和骨折最为常见。确诊年龄为 15.81 岁 [13.1; 16.8],所有患儿均发现 PTH、总钙和离子钙水平较高,其中 93.9% 的患者(n=46)患有低磷血症,43% 的患者(n=21)患有高钙尿症。49名患者中有5人(10.2%)发现甲状腺异位:3人位于甲状腺内,2人位于纵隔区。分子遗传学研究发现,32.7%的患者(n=16,CI (21; 47))存在基因突变,其中以MEN1基因突变最为常见(n=11)。在接受手术的39名患者中,84.6%的病例(n=33)发现了甲状腺腺瘤,7.7%的病例(n=3)发现了甲状腺增生,5.1%的病例(n=2)发现了甲状腺非典型腺瘤,5.1%的病例(n=2)发现了甲状腺癌: 本文介绍了小儿 PHPT 的病程特点和分子遗传学研究结果。该样本是俄罗斯联邦发表的样本中最大的。
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[Primary hyperparathyroidism in children].

Background:  Primary hyperparathyroidism (PHPT) is an endocrine disorder characterized by excessive secretion of parathyroid hormone (PTH) with upper-normal or elevated blood calcium levels due to primary thyroid gland pathology. PHPT is a rare pathology in children, with a prevalence of 2-5:100,000 children according to the literature. Due to the non-specificity of clinical manifestations at onset (nausea, vomiting, abdominal pain, emotional lability), the disease may remain undiagnosed for a long time.

Aim:  To study the features of the course and molecular genetic basis of primary hyperparathyroidism in children.

Materials and methods:  Retrospective observational study of 49 patients diagnosed with primary hyperparathyroidism. All patients underwent a comprehensive laboratory-instrumental and molecular genetic study at the Institute of Pediatric Endocrinology, Endocrinology Research Center of Russia in the period 2014-2022.

Results:  The first clinical symptoms of PHPT were noted at the age of 13.8 years [10.6; 1 5.2], among which fatigue, headaches, dyspepsia, lower limb pain, and fractures were the most common. The age of diagnosis was 15.81 years [13.1; 16.8], all children were found to have high levels of PTH, total and ionized calcium, with hypophosphatemia in 93.9% of patients (n=46) and hypercalciuria in 43% (n=21). Five out of 49 patients (10.2%) were found to have ectopy of the thyroid: 3 showed an intrathyroidal location, 2 in the mediastinal region. Molecular genetic study revealed mutations in 32.7% of patients (n=16, CI (21; 47)), mutations in MEN1 being the most frequent (n=11). Pathogenic variants in CDC73 were detected in 3 patients, RET - in 2. Among the operated 39 patients, adenoma of the thyroid was detected in 84.6% of cases (n=33), hyperplasia in 7.7% (n=3), atypical adenoma in 5.1% (n=2), carcinoma in 5.1% of cases (n=2).

Conclusion:  The paper presents the peculiarities of the course and the results of molecular genetic study of pediatric PHPT. This sample is the largest among those published in the Russian Federation.

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