Ye Yongsheng, Deng Fangyue, Luo Jiahui, Huang Xiongfei, Qu Xiliang, Zhuang Shabin
Department of Orthopedics, Dongguan Hospital of Traditional Chinese Medicine, Dongcheng District, Dongguan City, Guangdong Province, 523000, China.
J Surg Case Rep. 2023 Dec 28;2023(12):rjad689. doi: 10.1093/jscr/rjad689. eCollection 2023 Dec.
Spinal gout is a rare occurrence, and the combination of gout with lumbar spondylolysis has not been reported. We present a unique case involving a 29-year-old male who complained of low back pain for 1 month. Computed tomography and magnetic resonance imaging revealed articular subchondral erosions and a mass in the left L5-S1 facet joints. Initially treated for a spinal infection, the patient subsequently underwent lumbar spinal canal decompression and fusion, achieving complete relief. Postoperative pathology confirmed the spinal lesions to be tophaceous gout. Dual-energy CT or biopsy can assist in confirming the diagnosis. This report discusses another rare case of tophaceous gouty arthritis with spondylolysis to be added to the literature.
脊柱痛风较为罕见,痛风合并腰椎峡部裂的情况尚未见报道。我们报告一例独特病例,患者为一名29岁男性,主诉下腰痛1个月。计算机断层扫描和磁共振成像显示左L5-S1小关节软骨下侵蚀及肿块。患者最初按脊柱感染进行治疗,随后接受了腰椎管减压融合术,疼痛完全缓解。术后病理证实脊柱病变为痛风石性痛风。双能CT或活检有助于确诊。本报告讨论了另一例罕见的痛风石性痛风性关节炎合并峡部裂病例,以丰富文献资料。