Brown tumors in primary hyperparathyroidism initially interpreted as bone metastases and multiple gigantocelular tumors: case report.

Vedrana Gladić Nenadić, Marija Punda, Anita Tabain, Tomislav Jukić
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引用次数: 0

Abstract

Brown tumors or osteitis fibrosa cystica are a rare bone metabolism disorder that may mimic cancer metastasis. It represents a late manifestation of prolonged and mostly unrecognized hyperparathyroidism. In this case report we present a 44-year-old female patient with multiple lesions detected on bone scintigraphy and 18F- FDG-PET/CT, initially interpreted as a bone metastatic disease, rather than multiple gigantocellular bone tumors. Additionally, the presented case emphasizes the importance of a multidisciplinary approach in diagnosing brown tumors as part of hyperparathyroidism, and the treatment decision.

原发性甲状旁腺功能亢进的棕色肿瘤最初被解释为骨转移和多发性巨细胞瘤:1例报告。
棕色肿瘤或囊性纤维性骨炎是一种罕见的骨代谢紊乱,可能模仿癌症转移。它代表一种晚期表现的长期和大多未被认识甲状旁腺功能亢进。在这个病例报告中,我们报告了一位44岁的女性患者,在骨显像和18F- FDG-PET/CT上发现了多个病变,最初被解释为骨转移性疾病,而不是多发性巨细胞骨肿瘤。此外,本病例强调了多学科方法在诊断棕色肿瘤作为甲状旁腺功能亢进的一部分和治疗决策中的重要性。
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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