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甲状旁腺功能减退症的诊断与管理:希腊内分泌学会骨科学组工作组的建议

Diagnosis and management of hypoparathyroidism: recommendations of the working group of the Bone Section of the Hellenic Endocrine Society.

作者信息

Kassi Evanthia, Adamidou Fotini, Yavropoulou Maria P, Anastasilakis Athanasios D, Makras Polyzois, Vryonidou Andromachi, Tournis Symeon

机构信息

Centre of Expertise in Rare Endocrine Diseases, Endocrinology Unit, 1st Department of Propaedeutic Internal Medicine, C.E.R.E.D-Disorders of Calcium and Phosphate Metabolism (ENDO-ERN accredited), LAIKO General Hospital of Athens, National and Kapodistrian University of Athens, Athens, Greece.

Department of Endocrinology and Diabetes, Hippokratio General Hospital, Thessaloniki, Greece.

出版信息

Hormones (Athens). 2025 Jun 27. doi: 10.1007/s42000-025-00693-9.

Abstract

Hypoparathyroidism (HypoPT) is a rare endocrine disorder characterized by hypocalcemia accompanied by low or inappropriately normal parathyroid hormone (PTH) levels. The Bone Section of the Hellenic Endocrine Society reviewed the available evidence and the recent international guidelines and provided updated clinical practice recommendations for the diagnosis and optimal management of patients with HypoPT. Specifically, permanent post-surgical HypoPT should be considered if the disorder persists for more than 12 months after surgery, while in non-surgical cases, appropriate genetic testing should be applied, especially in young patients or those with syndromic features. In addition, the current report provides recommended and suggested laboratory and imaging examinations for the optimal management of patients with HypoPT. Concerning management, the panel recommends conventional therapy with calcium and vitamin D analogs as first-line treatment, while in patients with inadequate disease control, PTH replacement therapy should be considered with close monitoring. Finally, the challenges of the diagnosis and management of HypoPT in pregnancy are also discussed.

摘要

甲状旁腺功能减退症(HypoPT)是一种罕见的内分泌疾病,其特征为低钙血症,并伴有甲状旁腺激素(PTH)水平降低或正常但不适当。希腊内分泌学会骨科学组回顾了现有证据和近期国际指南,并为HypoPT患者的诊断和最佳管理提供了更新的临床实践建议。具体而言,如果该疾病在手术后持续超过12个月,则应考虑永久性术后HypoPT,而在非手术病例中,应进行适当的基因检测,尤其是在年轻患者或具有综合征特征的患者中。此外,本报告还提供了用于HypoPT患者最佳管理的推荐和建议的实验室及影像学检查。关于管理,专家组建议将钙和维生素D类似物的传统疗法作为一线治疗,而对于疾病控制不佳的患者,应考虑进行PTH替代疗法并密切监测。最后,还讨论了妊娠期间HypoPT诊断和管理的挑战。

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