Primary Hyperparathyroidism in the Common Orthopaedic Practice

N. Sferopoulos
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Abstract

An extensive review of the publications on primary hyperparathyroidism (pHPT) is presented in this report. It has strongly been emphasized in the literature that patients with pHPT may present either with the classical symptomatology or with asymptomatic disease, emerged due to biochemical screening. The clinical and epidemiological presentation of pHPT in western countries has changed profoundly during the past few decades, and bone disease is nowadays a distinct rarity. The introduction of serum calcium screening for osteoporosis and the technological advances in the laboratory assessment of parathyroid hormone have played important roles in early diagnosis. Subsequently, the disease is increasingly being detected as asymptomatic hypercalcaemia without guiding signs or symptoms. A third type of disease, the normocalcaemic variant, has been recently described in the literature. However, the potential diagnosis of pHPT should always be on the orthopaedics’ list of differential diagnoses in female or elderly patients with vertebral fractures and nephrolithiasis, either symptomatic or asymptomatic, as well as when solitary or multiple osteolytic lesions are encountered on the radiographs. Additionally, a middle aged woman with parathyroid adenoma and subsequent brown tumors detected on the pelvic radiographs is reported. Her initial laboratory findings indicated a minimal increase of the serum calcium, a mild increase of the erythrocyte sedimentation rate, and a significant increase in total serum alkaline phosphatase. Finally, the detection of elevated parathyroid hormone levels indicated the diagnosis of pHPT and necessitated imaging studies of the parathyroid glands, which indicated a parathyroid adenoma. Following successful excision of the parathyroid adenoma, the patient suffered from the hungry bone syndrome. After a follow-up of 20 years, the patient had normal calcium, vitamin D, and parathyroid hormone serum levels, while a pelvic radiograph indicated no significant changes in the appearance of the brown tumors.
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普通骨科实践中的原发性甲状旁腺功能亢进
本报告对原发性甲状旁腺功能亢进(pHPT)的出版物进行了广泛的回顾。文献强调,pHPT患者可能表现为经典症状,也可能表现为生化筛查后出现的无症状疾病。在过去的几十年里,pHPT在西方国家的临床和流行病学表现发生了深刻的变化,骨病现在已经非常罕见。骨质疏松症血清钙筛查的引入和甲状旁腺激素实验室检测技术的进步,对骨质疏松症的早期诊断起到了重要作用。随后,该病越来越多地被发现为无指导性体征或症状的无症状高钙血症。第三种类型的疾病,正钙血症变体,最近已在文献中描述。然而,对于患有椎体骨折和肾结石的女性或老年患者,无论是有症状的还是无症状的,以及在x线片上发现单发或多发溶骨性病变时,pHPT的潜在诊断应始终列入骨科的鉴别诊断清单。此外,一个中年妇女与甲状旁腺瘤和随后的棕色肿瘤盆腔x线片检测报告。她最初的实验室检查结果显示血清钙轻微升高,红细胞沉降率轻度升高,血清总碱性磷酸酶显著升高。最后,检测到甲状旁腺激素水平升高提示pHPT的诊断,需要对甲状旁腺进行影像学检查,提示甲状旁腺瘤。成功切除甲状旁腺瘤后,病人患上了饿骨综合征。经过20年的随访,患者的钙、维生素D和甲状旁腺激素血清水平正常,而盆腔x线片显示棕色肿瘤外观无明显变化。
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