一种罕见的溶解性病变原因:棕色肿瘤

Maroua Khaloui, F. Daoud, I. Rachdi, M. Somai, H. Zoubeidi, Z. Aydi, Nedia Hammam, Wided Hizem, B. Dhaou, F. Boussema
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引用次数: 0

摘要

原发性甲状旁腺功能亢进症(PHPT)是继糖尿病和甲状腺疾病之后第三常见的内分泌疾病,在绝经后妇女中发病率最高囊性纤维性骨炎或棕色肿瘤是甲状旁腺功能亢进依赖性骨病理的一种罕见临床表现,约3%的长期PHPT患者报道,2,3,在骨骼的不同部位有明确边界的放射学溶骨性病变。我们报告一个PHPT合并棕色肿瘤的病例,最初被误认为恶性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare cause of lytic lesion: the brown tumors
Primary hyperparathyroidism (PHPT) is the third most common endocrine disease after diabetes and thyroid disease with the highest incidence in postmenopausal women.1 Osteitis fibrosa cystica or Brown Tumors represent a rare clinical manifestation of hyperparathyroidism dependent bone pathology, reported in approximately 3% of patients with prolonged PHPT,2,3 and correspond to radiologically osteolytic lesions with well-defined borders in different parts of the skeleton. We illustrate a case of PHPT with brown tumor, which was initially mistaken for malignant disease.
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