Background <p>Spinal metalloma is a rare, space-occupying inflammatory pseudotumor caused by wear or corrosion of metallic spinal implants, which can lead to severe neurological compression. Although previously reported, cases arising from a biocompatible titanium alloy construct without evidence of implant failure or instability, and exhibiting direct dural invasion, are exceptionally rare, and their pathophysiology remains to be elucidated.</p> Case presentation <p>We report a 75-year-old male who presented with progressive low back pain, left lower limb radiculopathy, and cauda equina syndrome four years after undergoing an L3-5 posterior decompression, fusion, and titanium alloy instrumentation for lumbar spinal stenosis. Imaging studies ruled out infection, neoplasm, and implant loosening or breakage, but revealed a new, compressive intraspinal mass at the L2-3 level. Revision surgery revealed a grayish-black, sand-like necrotic mass severely compressing and invading an attenuated dura mater. Pathological examination confirmed tissue changes consistent with spinal metallosis. The patient’s neurological symptoms improved significantly postoperatively.</p> Results <p>A systematic literature review identified 8 similar cases. However, the present case is the first to be reported arising from a stable, all-titanium construct and featuring dural invasion.</p> Conclusions <p>A high index of suspicion for spinal metalloma should be maintained for patients presenting with new or progressive neurological symptoms after spinal surgery, even with a stable titanium alloy construct. Definitive diagnosis relies on histopathology, and adequate neurological decompression is the key to effective treatment.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Dural-Invasive spinal metalloma following titanium internal fixation: a rare case report and systematic literature review

  • Song Wang,
  • Ming Qian,
  • Jianru Xiao

摘要

Background

Spinal metalloma is a rare, space-occupying inflammatory pseudotumor caused by wear or corrosion of metallic spinal implants, which can lead to severe neurological compression. Although previously reported, cases arising from a biocompatible titanium alloy construct without evidence of implant failure or instability, and exhibiting direct dural invasion, are exceptionally rare, and their pathophysiology remains to be elucidated.

Case presentation

We report a 75-year-old male who presented with progressive low back pain, left lower limb radiculopathy, and cauda equina syndrome four years after undergoing an L3-5 posterior decompression, fusion, and titanium alloy instrumentation for lumbar spinal stenosis. Imaging studies ruled out infection, neoplasm, and implant loosening or breakage, but revealed a new, compressive intraspinal mass at the L2-3 level. Revision surgery revealed a grayish-black, sand-like necrotic mass severely compressing and invading an attenuated dura mater. Pathological examination confirmed tissue changes consistent with spinal metallosis. The patient’s neurological symptoms improved significantly postoperatively.

Results

A systematic literature review identified 8 similar cases. However, the present case is the first to be reported arising from a stable, all-titanium construct and featuring dural invasion.

Conclusions

A high index of suspicion for spinal metalloma should be maintained for patients presenting with new or progressive neurological symptoms after spinal surgery, even with a stable titanium alloy construct. Definitive diagnosis relies on histopathology, and adequate neurological decompression is the key to effective treatment.