Natural history of craniovertebral abnormalities in a single-center study in 54 patients with Hurler syndrome.

IF 2.1 3区 医学 Q3 CLINICAL NEUROLOGY Journal of neurosurgery. Pediatrics Pub Date : 2024-03-15 Print Date: 2024-06-01 DOI:10.3171/2024.1.PEDS23281
Shiwei Huang, David R Nascene, Ryan Shanley, Isabela Pena-Pino, Troy C Lund, Ashish O Gupta, Paul J Orchard, Carolina Sandoval-Garcia
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Abstract

Objective: Craniovertebral junction (CVJ) abnormalities are common and well documented in mucopolysaccharidosis type I-Hurler syndrome (MPS IH), often causing severe spinal canal narrowing. However, the requirement for surgical decompression and/or fusion is uncommon. Although hematopoietic cell transplant (HCT) has been shown to prolong the lives of patients with MPS IH, its effect in halting or reversing musculoskeletal abnormalities is less clear. Unfortunately, there are currently no universal guidelines for imaging or indication for surgical interventions in these patients. The goal of this study was to track the progression of the CVJ anatomy in patients with MPS IH following HCT, and to examine radiographic features in patients who needed surgical intervention.

Methods: Patients with MPS IH treated at the University of Minnesota with allogeneic HCT between 2008 and 2020 were retrospectively reviewed. Patients who underwent CVJ surgery were identified with chart review. All MPS IH cervical scans were examined, and the odontoid retroflexion angle, clivoaxial angle (CXA), canal width, and Grabb-Oakes distance (pB-C2) were measured yearly for up to 7 years after HCT. Longitudinal models based on the measurements were made. An intraclass correlation coefficient was used to measure interrater reliability. Nine children without MPS IH were examined for control CVJ measurements.

Results: A total of 253 cervical spine MRI scans were reviewed in 54 patients with MPS IH. Only 4 (7.4%) patients in the study cohort required surgery. Three of them had posterior fossa and C1 decompression, and 1 had a C1-2 fusion. There was no statistically significant difference in the spinal parameters that were examined between surgery and nonsurgery groups. Among the measurements, canal width and CXA varied drastically in patients with different neck positions. Odontoid retroflexion angle and CXA tended to decrease with age. Canal width and pB-C2 tended to increase with age.

Conclusions: Based on the data, the authors observed an increase in canal width and pB-C2, whereas the CXA and odontoid retroflexion angle became more acute as the patients aged after HCT. The longitudinal models derived from these data mirrored the development in children without MPS IH. Spinal measurements obtained on MR images alone are not sufficient in identifying patients who require surgical intervention. Symptom monitoring and clinical examination, as well as pathological spinal cord changes on MRI, are more crucial in assessing the need for surgery than is obtaining serial imaging.

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一项针对 54 名赫勒综合征患者的单中心研究显示了颅椎体异常的自然史。
目的:颅椎间隙(CVJ)异常在粘多糖病 I 型-赫勒综合征(MPS IH)中很常见,并有大量文献记载,通常会导致严重的椎管狭窄。然而,需要手术减压和/或融合的情况并不常见。虽然造血细胞移植(HCT)已被证明可延长 MPS IH 患者的生命,但其在阻止或逆转肌肉骨骼异常方面的效果并不明显。遗憾的是,目前还没有关于这些患者的影像学或手术干预指征的通用指南。本研究的目的是追踪 HCT 后 MPS IH 患者 CVJ 解剖学的进展,并检查需要手术干预的患者的影像学特征:回顾性分析明尼苏达大学在 2008 年至 2020 年间接受异基因 HCT 治疗的 MPS IH 患者。通过病历审查确定了接受 CVJ 手术的患者。研究人员检查了所有 MPS IH 颈椎扫描图像,并在 HCT 后长达 7 年的时间里每年测量蝶骨后屈角、颅椎角 (CXA)、椎管宽度和 Grabb-Oakes 距离 (pB-C2)。根据测量结果建立纵向模型。使用类内相关系数来衡量测量者之间的可靠性。9名未患MPS IH的儿童接受了对照CVJ测量:结果:54 名 MPS IH 患者共接受了 253 次颈椎 MRI 扫描。研究队列中只有 4 例(7.4%)患者需要手术治疗。其中3人接受了后窝和C1减压术,1人接受了C1-2融合术。手术组和非手术组的脊柱参数在统计学上没有明显差异。在测量结果中,不同颈部位置的患者的椎管宽度和CXA差异很大。随着年龄的增长,齿状突后屈角和 CXA 有减小的趋势。结论:根据这些数据,作者观察到随着 HCT 患者年龄的增长,椎管宽度和 pB-C2 会增加,而 CXA 和颌骨后屈角会变得更尖锐。根据这些数据得出的纵向模型反映了未患 MPS IH 儿童的发育情况。仅凭磁共振成像获得的脊柱测量结果不足以确定需要手术干预的患者。症状监测和临床检查以及核磁共振成像上的脊髓病理变化在评估手术需求方面比连续成像更为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of neurosurgery. Pediatrics
Journal of neurosurgery. Pediatrics 医学-临床神经学
CiteScore
3.40
自引率
10.50%
发文量
307
审稿时长
2 months
期刊介绍: Information not localiced
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