Diagnosing Spinal Gout: A Rare Case of Back Pain and Fever.

Case Reports in Rheumatology Pub Date : 2021-09-29 eCollection Date: 2021-01-01 DOI:10.1155/2021/7976420
Andres Cordova Sanchez, Maneesh Bisen, Farzam Khokhar, Adriana May, Jihad Ben Gabr
{"title":"Diagnosing Spinal Gout: A Rare Case of Back Pain and Fever.","authors":"Andres Cordova Sanchez,&nbsp;Maneesh Bisen,&nbsp;Farzam Khokhar,&nbsp;Adriana May,&nbsp;Jihad Ben Gabr","doi":"10.1155/2021/7976420","DOIUrl":null,"url":null,"abstract":"<p><p>Gout is a common inflammatory arthritis that has a high prevalence worldwide. It is characterized by monosodium urate deposition, usually affecting the joints and soft tissue of the lower extremities. Urate deposition in the axial skeleton resulting in spinal gout is rare. However, it seems to be more prevalent than usually thought, largely because it is underdiagnosed. Imaging findings are, for the most part, nonspecific and often mimic infectious etiologies. Definitive diagnosis requires pathological examination. Thus, it can be easily missed. We present a 41-year-old male with a seven-year history of untreated gout who came in with severe back pain, fevers, and radiculopathy. He was initially diagnosed with vertebral osteomyelitis. However, after a biopsy, spinal gout was confirmed. Spinal gout can be misdiagnosed as vertebral osteomyelitis given the similarities in presentation and imaging findings. This case report highlights the importance of keeping spinal gout as a differential of vertebral osteomyelitis, especially in patients with long-standing or uncontrolled gout with tophi.</p>","PeriodicalId":9622,"journal":{"name":"Case Reports in Rheumatology","volume":"2021 ","pages":"7976420"},"PeriodicalIF":0.0000,"publicationDate":"2021-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494596/pdf/","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Rheumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2021/7976420","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

Gout is a common inflammatory arthritis that has a high prevalence worldwide. It is characterized by monosodium urate deposition, usually affecting the joints and soft tissue of the lower extremities. Urate deposition in the axial skeleton resulting in spinal gout is rare. However, it seems to be more prevalent than usually thought, largely because it is underdiagnosed. Imaging findings are, for the most part, nonspecific and often mimic infectious etiologies. Definitive diagnosis requires pathological examination. Thus, it can be easily missed. We present a 41-year-old male with a seven-year history of untreated gout who came in with severe back pain, fevers, and radiculopathy. He was initially diagnosed with vertebral osteomyelitis. However, after a biopsy, spinal gout was confirmed. Spinal gout can be misdiagnosed as vertebral osteomyelitis given the similarities in presentation and imaging findings. This case report highlights the importance of keeping spinal gout as a differential of vertebral osteomyelitis, especially in patients with long-standing or uncontrolled gout with tophi.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
诊断脊柱痛风:一个罕见的病例背部疼痛和发烧。
痛风是一种常见的炎症性关节炎,在世界范围内具有很高的患病率。它的特点是尿酸钠沉积,通常影响关节和下肢软组织。尿酸沉积在轴骨导致痛风是罕见的。然而,它似乎比通常认为的更普遍,主要是因为它没有得到充分诊断。在大多数情况下,影像学发现是非特异性的,通常是模仿感染性病因。明确诊断需要病理检查。因此,它很容易被忽略。我们报告一位41岁男性患者,有7年未经治疗的痛风病史,他因严重的背部疼痛、发烧和神经根病而入院。他最初被诊断为脊椎骨髓炎。然而,活检后,脊髓性痛风被证实。脊柱痛风可误诊为椎体骨髓炎鉴于相似的表现和影像学表现。本病例报告强调了保持脊柱痛风作为椎体骨髓炎鉴别的重要性,特别是在长期或不受控制的痛风伴痛风患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
35
审稿时长
12 weeks
期刊最新文献
Severe Antiphospholipid Syndrome and Diffuse Glomerulonephritis After Adalimumab Treatment in a Patient With Ulcerative Colitis. Granulomatosis With Polyangiitis Mimicking Temporal Arteritis. Bing-Neel Syndrome: An Unknown GCA Mimicker. Mystical Myositis: A Case Series from Kalafong Provincial Tertiary Hospital, Pretoria, South Africa. Arthritis or an Adjacent Fascial Response? A Case Report of Combined Pyomyositis and Aseptic Arthritis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1