Department of Neurosurgery, King's College Hospital NHS Foundation Trust, London, United Kingdom.
GKT School of Medical Education, King's College London, London, United Kingdom.
World Neurosurg. 2020 Feb;134:507-509. doi: 10.1016/j.wneu.2019.10.198. Epub 2019 Nov 9.
Cauda equina syndrome (CES) is a neurosurgical emergency warranting urgent surgical decompression. Treatment delay may precipitate permanent adverse neurological sequelae. CES is a clinical diagnosis, corroborated by radiological findings. Atypical presentations should be acknowledged to avoid inappropriately rejected diagnoses.
We report the case of a woman exhibiting bilateral lower limb weakness, perineal numbness, sphincter disturbance, and lower limb clonus. Classically, CES displays lower motor neuron signs in the lower limbs. The presence of clonus, an upper motor neuron sign, brought the diagnosis into doubt. The history included chronic fatigue, difficulty mobilizing, and intermittent blurred vision. A lumbosacral magnetic resonance imaging (MRI) scan demonstrated a large disc prolapse at L5/S1. The cord was not low-lying or tethered. Therefore, the possibility of second diagnoses, including of inflammatory or demyelinating nature, was raised. An urgent MRI scan of the brain and cervicothoracic cord identified no other lesions. On balance, the clinical presentation could overwhelmingly be attributed to the L5/S1 disc prolapse. Given the time-critical nature of cauda equina (CE) compression, an urgent laminectomy and discectomy was offered with continued postoperative investigation of the clonus. Intraoperatively, significant CE compression was found. The operation proceeded uneventfully and the patient recovered fully. In the immediate postoperative period, the clonus persisted yet subsequently resolved completely.
We conclude that the clonus was attributable to CE compression and not a second pathology. The corresponding neuroanatomical correlate remains nondelineated. The presence of clonus does not preclude a diagnosis of CES. If the clinicoradiological information otherwise correlate, surgery should not be delayed while alternative diagnoses are sought. The literature is also reviewed.
马尾综合征(CES)是一种需要紧急手术减压的神经外科急症。治疗延迟可能导致永久性不良神经后遗症。CES 是一种临床诊断,辅以影像学发现。应认识到不典型表现,以避免不当拒绝诊断。
我们报告了一位女性患者的病例,其表现为双侧下肢无力、会阴部麻木、括约肌功能障碍和下肢阵挛。CES 经典表现为下肢下运动神经元体征。阵挛的出现,上运动神经元体征,使诊断受到质疑。病史包括慢性疲劳、移动困难和间歇性视力模糊。腰骶部磁共振成像(MRI)扫描显示 L5/S1 处有大的椎间盘突出。脊髓未低位或受牵拉。因此,提出了包括炎症或脱髓鞘性质在内的其他诊断的可能性。紧急脑和颈胸段脊髓 MRI 扫描未发现其他病变。总的来说,临床表现可以归因于 L5/S1 椎间盘突出。鉴于马尾(CE)受压的时间紧迫性,提供了紧急椎板切除术和椎间盘切除术,并在术后继续对阵挛进行检查。术中发现明显的 CES 受压。手术顺利进行,患者完全康复。在术后即刻,阵挛持续存在,但随后完全缓解。
我们得出结论,阵挛归因于 CES 受压,而不是第二种病理。相应的神经解剖学相关性仍不明确。阵挛的存在并不排除 CES 的诊断。如果临床和影像学信息相符,手术不应因寻找其他诊断而延迟。还回顾了文献。