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脊柱痛风石诱发的相邻节段疾病:一例报告

Adjacent segment disease induced by spinal tophus: a case report.

作者信息

Wang Chenglong, Liu Hongjun, Gong Shuangquan, Ye Yu, Cui Liqiang, Liu Dengshang, Li Sen, Xie Shiming

机构信息

Spinal Surgery Department, Mianyang Orthopaedic Hospital, Mianyang, Sichuan, China.

Division of Spine Surgery, Department of Orthopedic Surgery, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, China.

出版信息

Front Surg. 2025 May 14;12:1545557. doi: 10.3389/fsurg.2025.1545557. eCollection 2025.

DOI:10.3389/fsurg.2025.1545557
PMID:40438244
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12116555/
Abstract

Tophus, a hallmark feature of chronic gout, typically develops in the joints of the extremities, skin, and mucosal tissues. Although several case reports have described spinal tophus deposition leading to spinal stenosis and radiculopathy, documented cases of lumbar adjacent segment disease (ASD) caused by monosodium urate crystal (MUC) deposition remain exceedingly rare. Here, we report the case of a 56-year-old male who underwent L4-S1 lumbar fusion surgery two years prior for L4-S1 disc herniation with radiculopathy. The patient presented with recurrent low back pain, radiculopathy, and systemic tophus involvement. Magnetic resonance imaging (MRI) T2-weighted sequences revealed a hypointense signal at the posterior margin of the L3 vertebral body, while computed tomography (CT) demonstrated a hyperdense lesion. These radiographic findings suggested dural sac compression and spinal stenosis, though the definitive etiology warranted further evaluation. Surgical intervention involved excision of the L3 posterior lesion and extension of the fusion construct from L4-S1 to L2-S1 based on the existing L4-S1 instrumentation for spinal stabilization. Histopathological examination confirmed extensive MUC deposition. This report details the clinical presentation, imaging characteristics, pathological findings, surgical management, and potential pathogenic mechanisms underlying this rare complication.

摘要

痛风石是慢性痛风的标志性特征,通常出现在四肢关节、皮肤和黏膜组织中。尽管有几例病例报告描述了脊柱痛风石沉积导致椎管狭窄和神经根病,但由尿酸钠晶体(MUC)沉积引起的腰椎相邻节段疾病(ASD)的记录病例仍然极为罕见。在此,我们报告一例56岁男性病例,该患者两年前因L4-S1椎间盘突出伴神经根病接受了L4-S1腰椎融合手术。患者出现复发性腰痛、神经根病和全身性痛风石累及。磁共振成像(MRI)T2加权序列显示L3椎体后缘低信号,而计算机断层扫描(CT)显示高密度病变。这些影像学表现提示硬脊膜囊受压和椎管狭窄,尽管确切病因有待进一步评估。手术干预包括切除L3后部病变,并基于现有的L4-S1脊柱内固定器械将融合结构从L4-S1扩展至L2-S1以实现脊柱稳定。组织病理学检查证实有广泛的MUC沉积。本报告详细介绍了这种罕见并发症的临床表现、影像学特征、病理结果、手术治疗及潜在致病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f19/12116555/9eabc765bcd4/fsurg-12-1545557-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f19/12116555/90734f849a78/fsurg-12-1545557-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f19/12116555/9eabc765bcd4/fsurg-12-1545557-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f19/12116555/90734f849a78/fsurg-12-1545557-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f19/12116555/9eabc765bcd4/fsurg-12-1545557-g002.jpg

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