Case report: a rare combination of diffuse idiopathic skeletal hyperostosis and cervical septic spondylodiscitis

Denis Shakir, H. Tsonev, Kristian Ninov, Simeon Monov, Hristo Hristov
{"title":"Case report: a rare combination of diffuse idiopathic skeletal hyperostosis and cervical septic spondylodiscitis","authors":"Denis Shakir, H. Tsonev, Kristian Ninov, Simeon Monov, Hristo Hristov","doi":"10.35465/31.4.2023.pp112-122","DOIUrl":null,"url":null,"abstract":"Ossification of the anterior longitudinal ligament of the spine is a rare pathology with still unclear etiopathogenesis, although some authors associate it with metabolic diseases such as diabetes. Another rare disorder whose etiopathogenesis is also closely related to immunological disorders in diabetes is spinal epidural empyema. We present a case of a 62-year-old man with comorbidities of arterial hypertension and type II diabetes mellitus, with complaints of dysphagia and throat discomfort one and a half years prior to hospitalization. About a month before hospitalization, the patient reports pain with limited cervical mobility, followed by episodes of fever up to 38°C, with developing upper extremity muscle weakness and self-care incapacity. After imaging and laboratory studies, the patient was diagnosed with Forestier disease according to Resnick and Niwayama criteria, with ossification of the anterior longitudinal ligament and spondylodiscitis with epidural empyema in the cervical compartment. The patient was started on empiric antibiotic therapy and emergency surgery was undertaken for osteophytectomy, median corpectomy with medullar decompression and vertebrodesis. Postoperatively, the patient had improvement in dysphagia and upper extremity muscle strength - MRC 5/5 at the 6-month follow-up. Timely diagnosis and operative treatment with adequate decompression, anterior vertebrodesis and subsequent targeted antibiotic therapy are essential for a good outcome in the management of patients with this combined pathology.","PeriodicalId":380764,"journal":{"name":"Rheumatology (Bulgaria)","volume":"17 14","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rheumatology (Bulgaria)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35465/31.4.2023.pp112-122","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Ossification of the anterior longitudinal ligament of the spine is a rare pathology with still unclear etiopathogenesis, although some authors associate it with metabolic diseases such as diabetes. Another rare disorder whose etiopathogenesis is also closely related to immunological disorders in diabetes is spinal epidural empyema. We present a case of a 62-year-old man with comorbidities of arterial hypertension and type II diabetes mellitus, with complaints of dysphagia and throat discomfort one and a half years prior to hospitalization. About a month before hospitalization, the patient reports pain with limited cervical mobility, followed by episodes of fever up to 38°C, with developing upper extremity muscle weakness and self-care incapacity. After imaging and laboratory studies, the patient was diagnosed with Forestier disease according to Resnick and Niwayama criteria, with ossification of the anterior longitudinal ligament and spondylodiscitis with epidural empyema in the cervical compartment. The patient was started on empiric antibiotic therapy and emergency surgery was undertaken for osteophytectomy, median corpectomy with medullar decompression and vertebrodesis. Postoperatively, the patient had improvement in dysphagia and upper extremity muscle strength - MRC 5/5 at the 6-month follow-up. Timely diagnosis and operative treatment with adequate decompression, anterior vertebrodesis and subsequent targeted antibiotic therapy are essential for a good outcome in the management of patients with this combined pathology.
病例报告:罕见的弥漫性特发性骨骼增生症和颈椎化脓性脊盘炎合并症
脊柱前纵韧带骨化是一种罕见的病理现象,其发病机制尚不清楚,但一些学者认为它与糖尿病等代谢性疾病有关。另一种罕见疾病是脊柱硬膜外水肿,其发病机制也与糖尿病的免疫紊乱密切相关。我们接诊了一例 62 岁男性患者,合并动脉高血压和 II 型糖尿病,住院前一年半主诉吞咽困难和咽喉不适。住院前约一个月,患者报告颈部疼痛,活动受限,随后出现发热,最高温度达 38°C,并逐渐出现上肢肌肉无力和生活不能自理。经过影像学和实验室检查,根据雷斯尼克(Resnick)和尼瓦伊马(Niwayama)标准,患者被诊断为弗雷斯蒂埃病,颈椎前纵韧带骨化,脊椎盘炎,颈椎硬膜外水肿。患者开始接受经验性抗生素治疗,并接受了骨切除术、正中椎体切除术、髓核减压术和椎体穿刺术等紧急手术。术后,患者的吞咽困难和上肢肌力有所改善--6 个月随访时,MRC 为 5/5。及时诊断、充分减压的手术治疗、椎体前路穿刺术以及随后的针对性抗生素治疗对于治疗这种合并病症的患者取得良好疗效至关重要。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信