Parathyroid adenoma: multimodal diagnosis capabilities: A retrospective study

Nikolai A. Ognerubov, Tatiana S. Antipova, Galina N. Abakumova
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 Aim. To evaluate the current possibilities of multimodal diagnosis of parathyroid adenomas.
 Materials and methods. A retrospective analysis of 49 patients with primary hyperparathyroidism aged 24 to 82 (median 57.9 years) was performed. Modern radionuclide and hybrid technologies were used for topical diagnosis and metabolic assessment of parathyroid adenomas: scanning, single-photon emission computed tomography, single-photon emission computed tomography combined with computed tomography, positron emission tomography combined with computed tomography with 18F-deoxyglucose and 18F-choline. The diagnosis of primary hyperparathyroidism was confirmed by a biochemical blood test: the level of parathyroid hormone and ionized and total calcium.
 Results. The study included 43 (87.8%) females and 6 (12.2%) males. The female/male ratio was 7.2:1. Most cases (78.1%) were the hypercalcemic type of primary hyperparathyroidism, and the normocalcemic type was diagnosed in 21.9% of patients. The mean parathyroid hormone level was 145.43 pg/mL, exceeding the reference values by 2.2 times. Parathyroid hormone concentration in patients with primary hyperparathyroidism was 156.38 pg/mL, and mean ionized and total blood calcium levels were 1.43 and 3.04 mmol/L, respectively. The asymptomatic type occurred in 76.7% of patients. The symptomatic type of hyperparathyroidism had 23.3%, manifested with nephrolithiasis, pancreatitis, and bone lesions. Parathyroid adenomas were more often located in the left lobe (42.9%). In 77.6% of patients with primary hyperparathyroidism, solitary adenomas were detected. Ectopia of the parathyroid glands was detected in 16.3% of patients, with intrathyroidal location in the left lobe being the most common. Rare locations include the anterior and posterior mediastinum and the esophageal wall.
 Conclusion. Modern diagnostic multimodal options based on radionuclide and hybrid technologies are crucial in the personalized treatment of primary hyperparathyroidism.","PeriodicalId":10550,"journal":{"name":"Consilium Medicum","volume":"4 4","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Consilium Medicum","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26442/20751753.2023.6.202335","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Background. Primary hyperparathyroidism is a common endocrinological disease caused mainly by parathyroid adenoma. The main treatment method is surgery (parathyroidectomy). Therefore, the exact determination of adenoma localization is crucial. Aim. To evaluate the current possibilities of multimodal diagnosis of parathyroid adenomas. Materials and methods. A retrospective analysis of 49 patients with primary hyperparathyroidism aged 24 to 82 (median 57.9 years) was performed. Modern radionuclide and hybrid technologies were used for topical diagnosis and metabolic assessment of parathyroid adenomas: scanning, single-photon emission computed tomography, single-photon emission computed tomography combined with computed tomography, positron emission tomography combined with computed tomography with 18F-deoxyglucose and 18F-choline. The diagnosis of primary hyperparathyroidism was confirmed by a biochemical blood test: the level of parathyroid hormone and ionized and total calcium. Results. The study included 43 (87.8%) females and 6 (12.2%) males. The female/male ratio was 7.2:1. Most cases (78.1%) were the hypercalcemic type of primary hyperparathyroidism, and the normocalcemic type was diagnosed in 21.9% of patients. The mean parathyroid hormone level was 145.43 pg/mL, exceeding the reference values by 2.2 times. Parathyroid hormone concentration in patients with primary hyperparathyroidism was 156.38 pg/mL, and mean ionized and total blood calcium levels were 1.43 and 3.04 mmol/L, respectively. The asymptomatic type occurred in 76.7% of patients. The symptomatic type of hyperparathyroidism had 23.3%, manifested with nephrolithiasis, pancreatitis, and bone lesions. Parathyroid adenomas were more often located in the left lobe (42.9%). In 77.6% of patients with primary hyperparathyroidism, solitary adenomas were detected. Ectopia of the parathyroid glands was detected in 16.3% of patients, with intrathyroidal location in the left lobe being the most common. Rare locations include the anterior and posterior mediastinum and the esophageal wall. Conclusion. Modern diagnostic multimodal options based on radionuclide and hybrid technologies are crucial in the personalized treatment of primary hyperparathyroidism.
甲状旁腺瘤:多模式诊断能力:一项回顾性研究
背景。原发性甲状旁腺功能亢进是一种常见的内分泌疾病,主要由甲状旁腺瘤引起。主要的治疗方法是手术(甲状旁腺切除术)。因此,准确确定腺瘤的定位是至关重要的。 的目标。评价目前甲状旁腺瘤多模式诊断的可能性。 材料和方法。回顾性分析49例原发性甲状旁腺功能亢进患者,年龄24 ~ 82岁(中位57.9岁)。采用现代放射性核素及混合技术对甲状旁腺瘤进行局部诊断和代谢评估:扫描、单光子发射计算机断层扫描、单光子发射计算机断层扫描联合计算机断层扫描、正电子发射计算机断层扫描联合18f -脱氧葡萄糖和18f -胆碱。原发性甲状旁腺功能亢进症的诊断通过血液生化检查:甲状旁腺激素、离子和总钙水平;结果。其中女性43例(87.8%),男性6例(12.2%)。男女比例为7.2:1。大多数病例(78.1%)为原发性甲状旁腺功能亢进的高血钙型,21.9%的患者为正常血钙型。甲状旁腺激素平均值为145.43 pg/mL,超出参考值2.2倍。原发性甲状旁腺功能亢进症患者甲状旁腺激素浓度为156.38 pg/mL,平均血钙离子和总血钙水平分别为1.43和3.04 mmol/L。无症状型占76.7%。症状型甲状旁腺功能亢进占23.3%,表现为肾结石、胰腺炎和骨质损害。甲状旁腺瘤多位于左叶(42.9%)。77.6%的原发性甲状旁腺功能亢进患者检出单发性腺瘤。16.3%的患者有甲状旁腺异位,其中甲状腺内位于左叶最为常见。少见的部位包括前后纵隔和食管壁。 结论。基于放射性核素和混合技术的现代诊断多模式选择在原发性甲状旁腺功能亢进的个性化治疗中至关重要。
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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