Department of Pediatric Neurosurgery, Republican Specialized Scientific and Practical Medical Center of Neurosurgery, Tashkent 100142, Uzbekistan; Department of Neurosurgery, Tashkent Medical Academy, Tashkent 100109, Uzbekistan.
Department of Neurosurgery, Tashkent Medical Academy, Tashkent 100109, Uzbekistan.
Clin Neurol Neurosurg. 2024 Oct;245:108510. doi: 10.1016/j.clineuro.2024.108510. Epub 2024 Aug 14.
Split cord malformation and tethered cord syndrome are challenging pathologies in the pediatric population. During 2016-2022, 56 cases of split cord malformation (SCM) and tethered cord syndrome were treated at the Republican Specialized Scientific Medical Practical Center of Neurosurgery (RSSMPCN) of Uzbekistan. This article aims to provide a retrospective analysis of the clinical presentation, radiological findings, and surgical outcomes of patients with split cord malformation and tethered cord syndrome.
The retrospective study was conducted for 56 pediatric patients with split cord malformation and tethered cord syndrome during the abovementioned six-year period. All patients underwent MR imaging with computed tomography, followed by surgery with intraoperative neurophysiological monitoring. Each patient underwent follow-up examinations at 3 and 6 months postoperatively and yearly thereafter.
The mean patient age was 5.7 years (10 months to 15 years), and the male-to-female ratio was 1:2.2. Encouragingly, 44 (78.6 %) of the 56 patients showed improved neurological status postoperatively. Even in the cases where spur resection procedures were performed, there was partial neurological improvement, demonstrating the overall positive outcomes of the surgeries. Importantly, none of the 56 patients had neurological deteriorations in the postoperative period CONCLUSIONS: Split cord malformation is a rare but challenging pathology of childhood. The presentation is primarily characterized by movement, sensory or bowel disorders, and back and leg pain. This underscores the importance of early recognition and intervention when neurological symptoms are evident. Surgical intervention, as demonstrated in our study, is both appropriate and efficient in improving the neurological status of the patients.
脊髓分裂畸形和脊髓栓系综合征是儿科人群中具有挑战性的病理。在 2016 年至 2022 年期间,56 例脊髓分裂畸形(SCM)和脊髓栓系综合征患者在乌兹别克斯坦共和国神经外科专业科学实践中心(RSSMPCN)接受了治疗。本文旨在对脊髓分裂畸形和脊髓栓系综合征患者的临床表现、影像学表现和手术结果进行回顾性分析。
本回顾性研究对 56 例在上述六年期间患有脊髓分裂畸形和脊髓栓系综合征的儿科患者进行了研究。所有患者均行磁共振成像加计算机断层扫描检查,然后行术中神经生理监测下手术。每位患者在术后 3 个月和 6 个月以及此后每年进行随访检查。
患者的平均年龄为 5.7 岁(10 个月至 15 岁),男女比例为 1:2.2。令人鼓舞的是,56 例患者中有 44 例(78.6%)术后神经功能状态改善。即使进行了骨棘切除术,也有部分神经功能改善,表明手术总体上效果良好。重要的是,56 例患者中无 1 例在术后出现神经功能恶化。
脊髓分裂畸形是一种罕见但具有挑战性的儿童期病理。表现主要以运动、感觉或肠道功能障碍以及腰背和腿部疼痛为特征。这突出表明,当出现神经症状时,早期识别和干预至关重要。如我们的研究所示,手术干预在改善患者的神经功能方面既适当又有效。