医学
脊椎骨膜炎
外科
椎间盘炎
后凸
清创术(牙科)
骨髓炎
脊椎骨髓炎
脊柱融合术
腰椎
脊柱炎
椎间盘切除术
背痛
脓肿
软组织
减压
作者
Tobias Lange,Tobias L. Schulte,Viola Bullmann
出处
期刊:Spine
[Ovid Technologies (Wolters Kluwer)]
日期:2010-07-01
卷期号:35 (16): E804-E810
被引量:12
标识
DOI:10.1097/brs.0b013e3181d56955
摘要
In Brief Study Design. Case Report. Summary of Background Data. This report describes a patient who had 2 episodes of destructive spondylodiscitis occurring adjacent to levels at which surgery had previously been carried out due to an initial spondylodiscitis. A review of the literature did not reveal any equivalent cases. A comprehensive description of the management of this unusual course of spondylodiscitis is therefore presented here. Methods. Initially, the patient was suffering from L1-L2 spondylodiscitis caused by previous staphylococcal sepsis. After ineffective conservative antibiotic treatment, surgery was carried out, with posterior instrumentation and fusion at T11-L4 and removal and replacement of the L1 and L2 vertebral bodies. Results. After 2 months, the patient presented with paraparesis due to adjacent spondylodiscitis at T10-T11. The posterior instrumentation was therefore extended up to T9, and removal of the vertebral body of T11 was carried out. After 14 months, the patient was readmitted with pain and increased inflammatory parameters due to spondylodiscitis at T8/T9. Removal of the vertebral bodies was again carried out at T8 and T9, and posterior fusion up to T5 was performed. The patient received antibiotic treatment from 2 months before the first operation up to 3 months after surgery. Conclusion. Newly developing spondylodiscitis adjacent to a level at which a previous spondylodiscitis has been treated surgically is a rare condition, and aggressive treatment is necessary. This report describes a patient who had 2 episodes of spondylodiscitis occurring adjacent to levels at which surgery had been carried out due to an initial spondylodiscitis. A literature review did not reveal any equivalent cases. A comprehensive description of the management of this unusual course of spondylodiscitis is presented here.
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