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A型黏多糖贮积症患儿的颈胸段脊髓病:4例报告

Cervicothoracic myelopathy in children with Morquio syndrome A: a report of 4 cases.

作者信息

Baratela Wagner A R, Bober Michael B, Thacker Mihir M, Belthur Mohan V, Oto Murat, Rogers Kenneth J, Mackenzie William G

机构信息

Department of Orthopaedic Surgery, Alfred I duPont Hospital for Children, Wilmington, DE.

出版信息

J Pediatr Orthop. 2014 Mar;34(2):223-8. doi: 10.1097/BPO.0000000000000074.

Abstract

BACKGROUND

Craniovertebral junction anomalies and C1-C2 instability resulting in myelopathy have been well described in the literature on mucopolysaccharidosis IV (MPS-IV). Spinal involvement in MPS-IV patients, with neurological impairment, other than atlanto-axial instability and thoracolumbar kyphosis, has been scarcely mentioned in the literature.

METHODS

Retrospective clinical and radiologic review of the medical records and imaging studies of 4 individuals with Morquio A syndrome, who had undergone decompression and fusion of the cervicothoracic spine for myelopathy secondary to cervicothoracic stenosis between 1990 and 2009. Data regarding the presence of kyphosis at the cervicothoracic and upper thoracic spine, and neurological symptoms and signs were obtained.

RESULTS

There were 3 girls and 1 boy with an average age of 5 years and 11 months at presentation with neurological symptoms. Half of the patients had previously undergone occipitocervical fusion for atlanto-axial instability, whereas the other half were noted to have spinal cord compression at both the upper cervical and cervicothoracic regions, and underwent decompression and fusion at both levels concomitantly. All patients showed postoperative neurological improvement. All patients presented with the classical Morquio syndrome vertebral morphology. Cervicothoracic kyphosis was found in all of our patients in a varying severity (10 to 35 degrees). Levels of stenosis were similar in 3 patients, C7-T2; and occurred at a lower spinal level, T1-T4, in the remaining patient. Posterior disk bulging and thecal sac indentation were found in all 4 patients.

CONCLUSIONS

Neurological problems secondary to progressive kyphosis and stenosis at the cervicothoracic and upper thoracic spine are seen in children with Morquio syndrome. Early detection with a careful neurological assessment, whole spine MR imaging, and appropriate surgical treatment can prevent permanent neurological sequelae.

摘要

背景

颅颈交界区异常以及导致脊髓病的C1-C2不稳定在黏多糖贮积症IV型(MPS-IV)的文献中已有详尽描述。除寰枢椎不稳定和胸腰椎后凸外,MPS-IV患者伴有神经功能障碍的脊柱受累情况在文献中鲜有提及。

方法

对1990年至2009年间因颈胸段狭窄继发脊髓病而接受颈胸段脊柱减压融合术的4例莫尔基奥A综合征患者的病历和影像学研究进行回顾性临床及影像学分析。获取有关颈胸段和上胸段脊柱后凸情况以及神经症状和体征的数据。

结果

有3名女孩和1名男孩,出现神经症状时的平均年龄为5岁11个月。半数患者此前因寰枢椎不稳定接受了枕颈融合术,而另一半患者则在上颈椎和颈胸段均出现脊髓受压,并同时在两个节段进行了减压融合术。所有患者术后神经功能均有改善。所有患者均呈现典型的莫尔基奥综合征椎体形态。我们所有患者均存在不同程度(10至35度)的颈胸段后凸。3例患者的狭窄节段相似,为C7-T2;其余1例患者的狭窄节段位于较低的脊柱水平,即T1-T4。所有4例患者均发现椎间盘后凸和硬脊膜囊受压。

结论

莫尔基奥综合征患儿可见颈胸段和上胸段脊柱进行性后凸和狭窄继发的神经问题。通过仔细的神经评估、全脊柱磁共振成像早期发现并进行适当的手术治疗可预防永久性神经后遗症。

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