Fogwe Leslie, Ganipisetti Venu M, Naha Kushal
Internal Medicine, University of Missouri School of Medicine, Columbia, USA.
Hospital Medicine, Baystate Medical Center, Springfield, USA.
Cureus. 2024 Apr 30;16(4):e59376. doi: 10.7759/cureus.59376. eCollection 2024 Apr.
Brown tumors (also known as osteitis fibrosa cystica) are rare complications of end-stage renal disease (ESRD) and secondary hyperparathyroidism (HPT), characterized by focal bone lesions that resemble neoplasms. They are often misdiagnosed as metastatic bone disease, especially in patients with a history of malignancy. We present a case of a 60-year-old man with a history of renal cell carcinoma (RCC), and ESRD on hemodialysis (HD), who developed diffuse bone lesions on imaging with osteolytic/osteoblastic appearance concerning metastases, but on further workup was found to have brown tumors. We discuss the treatment and outcome and briefly review the relevant medical literature.
棕色瘤(也称为纤维囊性骨炎)是终末期肾病(ESRD)和继发性甲状旁腺功能亢进(HPT)的罕见并发症,其特征为类似肿瘤的局灶性骨病变。它们常被误诊为骨转移瘤,尤其是在有恶性肿瘤病史的患者中。我们报告一例60岁男性病例,该患者有肾细胞癌(RCC)病史,正在接受血液透析(HD)治疗的ESRD,影像学检查发现有弥漫性骨病变,呈溶骨/成骨表现,怀疑为转移瘤,但进一步检查发现是棕色瘤。我们讨论了治疗方法和结果,并简要回顾了相关医学文献。