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因手术切除被误诊为巨细胞骨肿瘤的肋部肿块后诊断出原发性甲状旁腺功能亢进症:一例报告

Primary hyperparathyroidism diagnosed after surgical ablation of a costal mass mistaken for giant-cell bone tumor: a case report.

作者信息

Vera Lara, Dolcino Mara, Mora Marco, Oddo Silvia, Gualco Marina, Minuto Francesco, Giusti Massimo

机构信息

Department of Internal Medicine, University of Genoa, Viale Benedetto XV, 6-16132, Genoa, Italy.

出版信息

J Med Case Rep. 2011 Dec 28;5:596. doi: 10.1186/1752-1947-5-596.

Abstract

INTRODUCTION

Primary hyperparathyroidism is a common endocrine disorder characterized by elevated parathyroid hormone levels, which cause continuous osteoclastic bone resorption. Giant cell tumor of bone is an expansile osteolytic tumor that contains numerous osteoclast-like giant cells. There are many similarities in the radiological and histological features of giant cell tumor of bone and brown tumor. This is a rare benign focal osteolytic process most commonly caused by hyperparathyroidism.

CASE PRESENTATION

We report the unusual case of a 40-year-old Caucasian woman in which primary hyperparathyroidism was diagnosed after surgical ablation of a costal mass. The mass was suspected of being neoplastic and histopathology was compatible with a giant cell tumor of bone. On the basis of the biochemical results (including serum calcium, phosphorous and intact parathyroid hormone levels) primary hyperparathyroidism was suspected and a brown tumor secondary to refractory hyperparathyroidism was diagnosed.

CONCLUSIONS

Since giant cell tumor is a bone neoplasm that has major implications for the patient, the standard laboratory tests in patients with bone lesions are important for a correct diagnosis.

摘要

引言

原发性甲状旁腺功能亢进是一种常见的内分泌疾病,其特征是甲状旁腺激素水平升高,导致持续性破骨细胞性骨吸收。骨巨细胞瘤是一种膨胀性溶骨性肿瘤,含有大量破骨细胞样巨细胞。骨巨细胞瘤和棕色瘤在放射学和组织学特征上有许多相似之处。这是一种罕见的良性局限性溶骨过程,最常见的原因是甲状旁腺功能亢进。

病例报告

我们报告了一例不寻常的病例,一名40岁的白种女性,在对肋骨肿块进行手术切除后被诊断为原发性甲状旁腺功能亢进。该肿块被怀疑为肿瘤性,组织病理学与骨巨细胞瘤相符。根据生化结果(包括血清钙、磷和完整甲状旁腺激素水平),怀疑为原发性甲状旁腺功能亢进,并诊断为继发性难治性甲状旁腺功能亢进的棕色瘤。

结论

由于骨巨细胞瘤是一种对患者有重大影响的骨肿瘤,对骨病变患者进行标准实验室检查对于正确诊断很重要。

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