由甲状旁腺功能亢进引起的溶骨性病变,模拟多发性骨转移

Kosuke Kita, Shigenori Nagata, Hironari Tamiya
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摘要

老年患者多发溶骨病变多为转移性骨肿瘤,而棕色肿瘤是一种罕见的疾病,以溶骨病变合并甲状旁腺功能亢进为特征。在这个报告中,我们提出了一个62岁的男性与甲状旁腺功能亢进诱导的多发性溶骨病变,模拟多发性转移性骨肿瘤的病例。在最初的表现中,x线图像与转移性骨肿瘤相符;因此,我们对髂溶性病变进行了穿刺活检,没有发现恶性肿瘤的证据。此外,我们对左侧桡骨病理性骨折进行了手术,并获得了足够的组织学检查样本,再次显示没有恶性肿瘤的证据。因此,在调查其他疾病时,我们发现左侧甲状腺肿瘤和高水平的完整甲状旁腺激素(PTH),这是诊断甲状旁腺瘤引起的PHPT的有力线索。切除甲状旁腺瘤后,完整的甲状旁腺素和钙水平恢复正常。总之,包括骨科专家在内的临床医生在出现上述临床特征时应考虑棕色肿瘤的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Osteolytic lesions caused by hyperparathyroidism mimicking multiple bone metastases
Multiple osteolytic lesions in elderly patients are usually metastatic bone tumors, while brown tumor is a rare disease featuring osteolytic lesions associated with hyperparathyroidism. In this report, we present the case of a 62-year-old male with hyperparathyroidism-induced multiple osteolytic lesions that mimicked multiple metastatic bone tumors. At initial presentation, the radiographic images were compatible with metastatic bone tumors; therefore, we performed a needle biopsy on the iliac lytic lesions, which revealed no evidence of malignancy. Furthermore, we performed an operation on the left radial pathological fracture and obtained sufficient sample for histological examination, which again showed no evidence of malignancy. Hence, while investigating for other diseases, we found a tumor in the left thyroid and high levels of intact-parathyroid hormone (PTH), which was a strong clue to the diagnosis of PHPT caused by a parathyroid adenoma. After the resection of the parathyroid adenoma, intact-PTH and calcium levels returned to normal. In conclusion, clinicians including orthopedic specialists should consider the possibility of brown tumors in case of aforementioned clinical features.
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