Features of the diagnosis of primary hyperparathyroidism in children

A. V. Gostimskiy, Z. Matveeva, A. Romanchishen, I. V. Karpatskiy, A. Kuzmichev, S. Peredereev, D. V. Makharoblishvili
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Abstract

Background. Primary hyperparathyroidism (PHPT) is a rare pathology in pediatric and adolescent patients. Collection, analysis and generalization of the literature data and experience of the leading clinics allow to develop unified, statistically substantiated approaches to diagnostics and surgical treatment of this group of patients.Material and methods. The article presents a retrospective analysis of 17 cases of PHPT in children and adolescents aged from 6 to 18 years operated on in the department of Surgery of St.-Petersburg State Pediatric Medical University in the period from 1973 till 2021. Among those operated there were 10 girls and 7 boys, the M:F ratio was 1:1.4. The mean age of the patients was 12,9±0,71 years.Results and discussion. The main criteria of the disease diagnosis were elevated blood calcium and parathormone levels, excessive urinary calcium secretion. Manifest forms of the disease were diagnosed in 10 (58,8%) of 17 children. In 3 (17,6%) cases the parathyroid neoplasms were accompanied neither by clinical, nor laboratory manifestations of the disease and were regarded as incidentalomas. Another 4 (23.5%) patients had only laboratory changes (hypercalcemia and hyperparathyrinaemia) that manifested themselves preoperatively. These observations were referred to the asymptomatic form of PHPT.In 7 (41.2%) cases parathyroid adenomas were found and removed during surgeries for various thyroid diseases (thyroid cancer in 5 cases, diffuse toxic goiter in 1 case). An incidental finding of parathyroid adenoma was during prophylactic thyroidectomy for Sipple syndrome.A radioisotope method proved to be the most informative way to localize parathyroid tumors.Conclusion. The diagnosis of the disease in manifest sporadic cases does not differ from that in adults. Genetic study is indicated in the presence of a family history of multiple involvement of the parathyroid glands. Surgical treatment with removal of parathyroid tumor is the main method, which allows to achieve complete recovery. 
儿童原发性甲状旁腺功能亢进的诊断特点
背景原发性甲状旁腺功能亢进症(PHPT)在儿童和青少年患者中是一种罕见的病理学。通过收集、分析和总结领先诊所的文献数据和经验,可以开发出统一的、有统计依据的方法来诊断和治疗这类患者。材料和方法。本文对1973年至2021年在圣彼得堡国立儿科医科大学外科手术的17例6至18岁儿童和青少年PHPT病例进行了回顾性分析。手术者中有10名女孩和7名男孩,男女比例为1:1.4。患者的平均年龄为12.9±0.71岁。结果和讨论。疾病诊断的主要标准是血钙和甲状旁腺激素水平升高、尿钙分泌过多。17名儿童中有10名(58.8%)被诊断为明显的疾病。在3例(17.6%)病例中,甲状旁腺肿瘤既没有临床表现,也没有实验室表现,被视为偶发性牙瘤。另有4名(23.5%)患者在术前仅出现实验室变化(高钙血症和甲状旁腺素血症)。这些观察结果被称为无症状形式的PHPT。在7例(41.2%)病例中,在各种甲状腺疾病的手术中发现并切除了甲状旁腺腺瘤(5例为甲状腺癌症,1例为弥漫性毒性甲状腺肿)。在预防性甲状腺切除术治疗Sipple综合征期间偶然发现甲状旁腺腺瘤。放射性同位素方法被证明是定位甲状旁腺肿瘤的最有信息的方法。结论这种疾病在明显散发病例中的诊断与在成人中的诊断没有区别。遗传研究表明存在甲状旁腺多发性受累的家族史。切除甲状旁腺肿瘤的手术治疗是实现完全康复的主要方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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