Giant Parathyroid Adenoma-Associated Fracture, Not All Lytic Bone Lesions are Cancer: A Case-Based Review.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Case Reports in Medicine Pub Date : 2022-01-29 eCollection Date: 2022-01-01 DOI:10.1155/2022/3969542
Jose C Alvarez-Payares, Marcel E Ribero, Sara Ramírez-Urrea, María C Fragozo-Ramos, Jose E Agámez-Gómez, Alejandro Román-González, Luis F Arias, Roberto Benavides Arenas, Fernando López-Urbano
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引用次数: 1

Abstract

Introduction: Due to the early diagnosis of primary hyperparathyroidism the musculoskeletal manifestations of this disease are becoming less frequent. When this disease manifests secondary to a giant adenoma, it presents with more aggressive symptoms and can have important repercussions such as the hungry bone syndrome after parathyroidectomy. There are few reported cases of hyperparathyroidism secondary to a giant adenoma in the literature, as the presence of a brown tumor is often misinterpreted as a metastatic lesion from an unknown primary tumor.

Methods: We describe a case and performed a literature review to identify all case reports. A literature search was carried out on PubMed/MEDLINE and EMBASE bibliographic databases. All available studies from May 2009 to May 2021 were included. Data were tabulated, and outcomes were cumulatively analyzed.

Results: Twenty-four cases of primary hyperparathyroidism due to giant adenoma have been described; the majority were women, with a mean age of 52 years. They presented with heterogeneous symptoms such as palpable nodules (45%), bone pain (33%), brown tumor (12.5%), asymptomatic (12.5%), metabolic profile with a mean calcemia of 13.8 mg/dL, PTH 1109 ng/L, and mean tumor weight of 47.24 g.

Conclusion: Primary hyperparathyroidism due to giant adenoma increases the risk of developing potentially serious postoperative complications such as hungry bone syndrome. This implies the need of implementing preventive measures comprising administration of intravenous zoledronic acid and early supplementation of oral calcium to prevent complications after resection.

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巨大甲状旁腺腺瘤相关骨折,并非所有溶解性骨病变都是癌症:一项基于病例的回顾。
简介:由于原发性甲状旁腺功能亢进的早期诊断,这种疾病的肌肉骨骼表现越来越少见。当这种疾病继发于巨大腺瘤时,它会出现更具侵袭性的症状,并可能产生重要的影响,如甲状旁腺切除术后的饥饿骨综合征。在文献中,继发于巨大腺瘤的甲状旁腺功能亢进病例报道很少,因为棕色肿瘤常被误解为未知原发肿瘤的转移灶。方法:我们描述了一个病例,并进行了文献综述,以确定所有病例报告。在PubMed/MEDLINE和EMBASE书目数据库中进行文献检索。纳入了2009年5月至2021年5月的所有可用研究。将数据制成表格,并对结果进行累积分析。结果:报告了24例原发性甲状旁腺功能亢进合并巨大腺瘤的病例;大多数是女性,平均年龄为52岁。他们表现出异质性症状,如可触及结节(45%),骨痛(33%),棕色肿瘤(12.5%),无症状(12.5%),代谢谱平均钙含量为13.8 mg/dL, PTH为1109 ng/L,平均肿瘤重量为47.24 g。结论:巨大腺瘤引起的原发性甲状旁腺功能亢进增加了发生诸如饿骨综合征等潜在严重术后并发症的风险。这意味着需要实施预防措施,包括静脉注射唑来膦酸和早期补充口服钙,以防止术后并发症。
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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来源期刊
Case Reports in Medicine
Case Reports in Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
0.00%
发文量
53
审稿时长
13 weeks
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