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Cauda Equina Syndrome Associated with Dural Ectasia in Chronic Anlylosing Spondylitis

机译:慢性强直性脊柱炎伴硬脑膜扩张的马尾综合征

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摘要

Cauda equina syndrome (CES) associated with dural ectasia is a rare neurologic complication in patients with longstanding ankylosing spondylitis (AS). We report a 68-year-old male with a 30-year history of AS who presented a typical symptom and signs of progressive CES, urinary incontinence and neuropathic pain of the lumbosacral radiculopathy. Computed tomography (CT) and magnetic resonance imaging (MRI) findings showed the unique appearances of dural ectasia, multiple dural diverticula, erosion of posterior element of the lumbar spine, tethering of the conus medullaris and adhesion of the lumbosacral nerve roots to the posterior aspect of the dural ectasia. Considering the progressive worsening of the clinical signs, detethering of the conus medullaris through resection of the filum terminale was performed through a limited laminectomy. However, the urinary incontinence did not improve and there was a partial relief of the neuropathic leg pain only. The possible pathogenetic mechanism of CES-AS and the dural ectasia in this patient with longstanding AS are discussed with a literature review.
机译:与硬脑膜扩张相关的马尾神经综合征(CES)在患有强直性脊柱炎(AS)的患者中是一种罕见的神经系统并发症。我们报告了一位68岁的男性,有30年的AS病史,他表现出典型的症状和进行性CES,小便失禁和腰s神经根神经痛的迹象。计算机断层扫描(CT)和磁共振成像(MRI)结果显示硬脑膜扩张,硬脑膜憩室多发,腰椎后部元件侵蚀,圆锥延髓系留以及腰s神经根向后方的粘附硬脑膜扩张。考虑到临床症状的逐步恶化,通过有限的椎板切除术通过切除terminal末端对延髓进行束缚。但是,尿失禁并没有改善,仅部分缓解了神经性腿痛。文献复习讨论了该患者长期存在AS的CES-AS和硬脑膜扩张的可能致病机理。

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