儿童特发性脊髓空洞-影像学和临床结果随访至成年期。

Rosa Sun, Pritsana Punyawai, Navin Furtado, Fardad T Afshari, Pasquale Gallo
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引用次数: 0

摘要

目的:特发性脊髓空洞症(IS)被定义为没有可识别的原发病理的脊髓空洞。儿童IS患者的自然病史、临床意义和放射学治疗仍然知之甚少,现有文献提供的长期数据有限。本研究旨在评估儿童IS患者的长期临床和放射学预后,重点了解临床或放射学进展的预测因素,以及临床和放射学进展之间的相关性。方法:本回顾性研究纳入28例诊断为IS的儿科患者,所有患者均进行了至少三年的放射随访。排除上游病理引起的继发性鼻鸣。对临床和影像学资料进行分析,以评估鼻窦的放射学变化和症状的变化。探讨了影像学与临床特征的相关性。结果:中位放射学随访时间和临床随访时间分别为6.84年和7.66年。53.6%的患者鼻管缩小(宽度或前后直径≥1mm),与性别、诊断年龄、初始鼻管大小或脊柱侧凸无显著相关性。25%的患者出现背痛;其他表现形式包括泌尿系统障碍和神经功能障碍。所有患者在随访期间均保持临床无症状、稳定或改善。影像学改变与临床结果无关。没有发现放射学或临床结果的预测因子。结论:小儿IS患者以良性病程为主,影像学改变显示临床相关性不大。在病情稳定的病例中,重复间隔成像似乎是不必要的,治疗应优先考虑临床症状。这项研究提供了迄今为止最大的长期数据集,支持保守的IS管理方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paediatric idiopathic syringomyelia - a follow-up of radiological and clinical outcomes into adulthood.

Objective: Idiopathic syringomyelia (IS) is defined by the presence of a spinal syrinx without identifiable primary pathology. The natural history, clinical implications, and radiological management of IS in the paediatric patient remain poorly understood, with existing literature providing limited long-term data. This study aims to evaluate the long-term clinical and radiological outcomes of paediatric patients with IS, focusing on understanding predictive factors of clinical or radiological progression, and the correlation between clinical and radiological evolution.

Methods: This retrospective study included 28 paediatric patients diagnosed with IS, all with a minimum of three years of radiological follow-up. Cases of secondary syrinx caused by upstream pathology were excluded. Clinical and imaging data were analysed to assess the radiological change of the syrinx and change in symptoms. Correlations between radiological and clinical features were explored.

Results: The median radiological and clinical follow-up durations were 6.84 years and 7.66 years, respectively. A reduction in syrinx size (≥ 1 mm in width or anterior-posterior diameter) was observed in 53.6% of patients, with no significant association with gender, age at diagnosis, initial syrinx size, or scoliosis. Back pain occurred in 25% of patients; other modes of presentation include urological disturbance and neurological deficits. All patients remained clinically asymptomatic, stable or improved during follow-up. Radiological changes did not correlate with clinical outcomes. No predictors were found for radiological or clinical outcomes.

Conclusions: IS in paediatric patients follow a predominantly benign course, with radiological changes showing little clinical relevance. Repeated interval imaging appears unnecessary in stable cases, and management should prioritise clinical symptoms. This study provides the largest long-term dataset to date, supporting a conservative approach to IS management.

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