多发性棕色瘤伴原发性甲状旁腺功能亢进症，酷似骨转移瘤[]。
Multiple brown tumors with primary hyperparathyroidism mimicking bone metastases [].
作者信息
Ngo Quy X, Ngo Duy Q, Tran Toan D, Le Duong T, Hoang Giap N, Le Quang V
机构信息
Department of Head and Neck Surgery, Vietnam National Cancer Hospital, 30 Cau Buou Street, Thanh Tri District, Hanoi, Viet Nam.
Hanoi Medical University, 01 Ton That Tung Street, Dong Da District, Hanoi, Viet Nam.
出版信息
Int J Surg Case Rep. 2021 Feb;79:375-378. doi: 10.1016/j.ijscr.2021.01.002. Epub 2021 Jan 18.
Multiple osteolytic lesions are usually associated with bone metastasis. However, brown tumor should also be included in the differential diagnosis. Brown tumor is a rare benign lesions in skeletal system, encountered in patients with uncontrolled primary or secondary hyperparathyroidism. In our case report, we present a 35-year-old female with multifocal brown tumor that difficultiy in differential diagnosis of metastasis of malignant parathyroid. Additionally, the treatment and follow up after parathyroidectomy are also emphasized. METHODS: The SCARE 2020 Guideline [1].
多发性溶骨性病变通常与骨转移有关。然而，棕色瘤也应列入鉴别诊断范围。棕色瘤是骨骼系统中一种罕见的良性病变，见于原发性或继发性甲状旁腺功能亢进未得到控制的患者。在我们的病例报告中，我们介绍了一名35岁女性，患有多灶性棕色瘤，难以与恶性甲状旁腺转移瘤进行鉴别诊断。此外，还强调了甲状旁腺切除术后的治疗和随访。方法：采用SCARE 2020指南[1]。
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