Sun Rosa, Punyawai Pritsana, Furtado Navin, Afshari Fardad T, Gallo Pasquale
Birmingham Children's Hospital, Steelhouse Lane, Queensway, Birmingham, UK.
Queen Elizabeth Hospital, Mindelsohn Way, Birmingham, UK.
Childs Nerv Syst. 2025 Jul 16;41(1):236. doi: 10.1007/s00381-025-06885-3.
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.
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.
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.
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.
特发性脊髓空洞症(IS)的定义是存在脊髓空洞且无明确的原发性病理改变。小儿患者IS的自然病史、临床意义及放射学处理仍知之甚少,现有文献提供的长期数据有限。本研究旨在评估小儿IS患者的长期临床和放射学结局,重点了解临床或放射学进展的预测因素以及临床与放射学演变之间的相关性。
本回顾性研究纳入28例诊断为IS的小儿患者,所有患者均有至少3年的放射学随访。排除由上游病变引起的继发性脊髓空洞症病例。分析临床和影像学数据,以评估脊髓空洞的放射学变化和症状变化。探讨放射学与临床特征之间的相关性。
放射学和临床随访的中位时长分别为6.84年和7.66年。53.6%的患者脊髓空洞大小缩小(宽度或前后径≥1mm),与性别、诊断时年龄、初始脊髓空洞大小或脊柱侧弯无显著关联。25%的患者出现背痛;其他表现形式包括泌尿系统紊乱和神经功能缺损。所有患者在随访期间临床症状均保持无症状、稳定或改善。放射学变化与临床结局无关。未发现放射学或临床结局的预测因素。
小儿IS患者的病程主要呈良性,放射学变化的临床相关性较小。对于病情稳定的病例,似乎无需定期重复成像,治疗应优先考虑临床症状。本研究提供了迄今为止最大的长期数据集,支持对IS采取保守治疗方法。