创伤后脊髓畸形1例报告

Izzat Zulhilmi Abd Rahman, Salmah Anim Abu Hassan
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摘要

背景和目的:管腔畸形是一种罕见的进行性神经系统疾病,其特征是脑干内存在管腔或充满液体的细长腔,可能有多种潜在病因。然而,迄今为止,只有少数病例的脊髓空洞表现为创伤后脊髓空洞(PTS)的晚期并发症已被报道。方法:我们报告了一位26岁的病态肥胖男士,在T7爆裂骨折2年后出现T4 AIS C不完全性脊髓损伤,需要脊柱内固定。1年后,他经历了种植体失败,需要取出种植体。随后,他报告背部疼痛加重,左上肢和下肢神经系统恶化。除此之外,左上肢的疼痛和肌肉痉挛一直延伸到颈部、面部和头部的左侧,需要对大脑和脊髓进行重复成像。磁共振成像(MRI)显示脊髓空洞主要影响延髓左侧,伴广泛起源于C1至T12椎体水平的脊髓空洞。此外,老T7骨折部位仍然不愈合。结果:尽管成功进行了第二次脊柱减压手术和综合康复,但没有神经功能恢复。然而,患者描述了疼痛和痉挛的显著改善。结论:PTS合并脊髓弓根畸形虽罕见,但却是脊髓损伤患者迟发性神经功能恶化的原因之一。这可能是一个诊断困境,因为一些病例表现出非典型的表现,并模仿先前存在的神经缺陷。创伤后脊柱畸形患者由于蛛网膜下腔脑脊液(CSF)流动改变而形成的鼻咽可能受益于减压手术,避免了硬膜内分流术的放置,再加上药物和物理治疗。尽管没有神经恢复,神经性疼痛和痉挛的症状缓解提高了生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Uncommon Case of Post-Traumatic Syringobulbia: A Case Report
Background and aim: Syringobulbia is a rare progressive neurological condition characterised by the presence of syrinx or an elongated fluid-filled cavity in the brainstem with multiple possible underlying aetiologies. However, to date, only a few cases of syringobulbia presenting as a late complication of post-traumatic syringomyelia (PTS) have been reported. Methods: We present a case of a 26-year-old morbidly obese gentleman with T4 AIS C incomplete spinal cord injury following T7 burst fracture 2 years prior requiring spinal instrumentation. He then experienced implant failure 1 year later, necessitating implant removal. Subsequently, he reported worsening back pain and neurology deterioration over his left upper and lower limb. In addition to that, pain and muscle spasms over the left upper limb extending up to the left side of his neck, face, and head warranted a repeat imaging of the brain and spinal cord. Magnetic resonance imaging (MRI) revealed syringobulbia predominantly affecting the left side of the medulla oblongata with extensive syringomyelia originating from the C1 to T12 vertebral level. Moreover, the old T7 fracture site remained malunited. Results: Despite a successful second spinal decompressive surgery and combined rehabilitation, there was no neurological recovery. However, the patient described significant improvement in pain and spasms. Conclusion: PTS complicated with syringobulbia, although rare, is one of the causes of the delayed-onset neurological deterioration in spinal cord injured patients. It might be a diagnostic dilemma as some cases exhibit atypical presentations and mimic the pre-existing neurological deficit. Syrinx formation due to alteration of subarachnoid cerebrospinal fluid (CSF) flow in post-traumatic spinal deformity might benefit from decompressive surgery, avoiding the need for intradural shunt placement, coupled with medication and physical therapy. Even though there was no neurological recovery, symptomatic alleviation of neuropathic pain and spasm improved quality of life.
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