脐带分裂畸形和脐带系带综合征的治疗:乌兹别克斯坦一家主要转诊中心的经验

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY
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引用次数: 0

摘要

背景脊髓分裂畸形和脊髓系带综合征是儿科中极具挑战性的病症。2016-2022 年间,乌兹别克斯坦共和国神经外科专业科学医疗实践中心(RSSMPCN)共收治了 56 例脊髓分裂畸形(SCM)和系带综合征患者。本文旨在对脊髓分裂畸形和脊髓系带综合征患者的临床表现、放射学检查结果和手术治疗效果进行回顾性分析。方法对上述六年期间的 56 名脊髓分裂畸形和脊髓系带综合征儿科患者进行回顾性研究。所有患者均接受了核磁共振成像和计算机断层扫描,随后进行了手术,术中进行了神经电生理监测。结果患者平均年龄为 5.7 岁(10 个月至 15 岁),男女比例为 1:2.2。令人鼓舞的是,56 名患者中有 44 人(78.6%)术后神经状况有所改善。即使是进行了骨刺切除手术的病例,其部分神经功能也得到了改善,这表明手术的总体效果良好。结论脊髓分裂畸形是一种罕见但具有挑战性的儿童病症。其主要表现为运动、感觉或排便障碍,以及背部和腿部疼痛。这强调了在出现明显神经症状时及早识别和干预的重要性。正如我们的研究所示,手术干预对于改善患者的神经状况既恰当又有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of split cord malformation and tethered cord syndrome: Experience of a main referral center in Uzbekistan

Background

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.

Methods

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.

Results

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.

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来源期刊
Clinical Neurology and Neurosurgery
Clinical Neurology and Neurosurgery 医学-临床神经学
CiteScore
3.70
自引率
5.30%
发文量
358
审稿时长
46 days
期刊介绍: Clinical Neurology and Neurosurgery is devoted to publishing papers and reports on the clinical aspects of neurology and neurosurgery. It is an international forum for papers of high scientific standard that are of interest to Neurologists and Neurosurgeons world-wide.
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