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高位截瘫轮椅运动员因慢性颈脊髓病急性发作致颈段肌阵挛:1 例报告。

Acute on chronic cervical myelopathy causing cervical segmental myoclonus in a high-level wheelchair athlete: a case report.

机构信息

Cleveland Clinic Children's Hospital, Cleveland, OH, USA.

Cleveland Clinic Children's Hospital for Rehabilitation, Cleveland, OH, USA.

出版信息

Spinal Cord Ser Cases. 2021 Sep 29;7(1):90. doi: 10.1038/s41394-021-00453-y.

DOI:10.1038/s41394-021-00453-y
PMID:34588415
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8481506/
Abstract

INTRODUCTION

This is a 20-year-old wheelchair athlete with history of caudal regression syndrome and cervical canal stenosis who developed spinal segmental myoclonus following routine intubation for an elective procedure.

CASE PRESENTATION

This patient is a 20-year-old man with history of caudal regression syndrome and chronic cervical stenosis. He is a high-level wheelchair racer and paralympic hopeful. This patient initially presented 18 months prior with shoulder abduction weakness. He was found to have cervical stenosis at C4, C5 on MRI. Neurosurgical treatment was not needed at that time as symptoms resolved. On this encounter, he presented for an elective urologic surgical procedure. Glidescope intubation was performed with notable cervical extension. In the Post Anesthesia Care Unit, the patient began experiencing twitching movements in his pectoral muscles bilaterally as well as left deltoid and biceps. His findings were consistent with myoclonus due to his cervical myelopathy. He was initially started on levetiracetam, but experienced dizziness. His symptoms were finally controlled with clonazepam. Neurosurgery performed cord decompression and fusion with resolution of his symptoms.

DISCUSSION

There are few cases of myoclonus secondary to myelopathy documented in literature. The current recommended treatments, levetiracetam and/or benzodiazepines, were successful in managing the myoclonus in this patient. However, cord decompression is necessary to avoid progression of myelopathic symptoms. In conclusion, myoclonus can be a presenting symptom of myelopathy and warrants further investigation, especially in patients with known spinal cord or vertebral pathology.

摘要

引言

这是一位 20 岁的轮椅运动员,患有尾骨退化综合征和颈椎管狭窄症,在常规插管进行择期手术时出现脊髓节段性肌阵挛。

病例介绍

该患者为 20 岁男性,患有尾骨退化综合征和慢性颈椎狭窄症。他是一名高水平轮椅赛车手,有望参加残奥会。该患者最初于 18 个月前出现肩部外展无力。MRI 显示 C4、C5 颈椎狭窄。当时由于症状缓解,不需要神经外科治疗。此次就诊时,他因择期泌尿科手术而来。在麻醉后护理单元,患者开始出现双侧胸肌、左侧三角肌和肱二头肌抽搐。由于他的颈椎脊髓病,他的发现与肌阵挛一致。他最初开始使用左乙拉西坦,但出现头晕。他的症状最终通过氯硝西泮得到控制。神经外科进行了脊髓减压和融合,症状得到缓解。

讨论

文献中很少有因脊髓病引起的肌阵挛病例。目前推荐的治疗方法是左乙拉西坦和/或苯二氮䓬类药物,这些方法成功地控制了该患者的肌阵挛。然而,需要进行脊髓减压以避免脊髓病症状的进展。总之,肌阵挛可能是脊髓病的一个表现症状,需要进一步调查,特别是在已知有脊髓或脊柱病理的患者中。

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Spinal myoclonus: a rare presentation of cervical myelopathy.脊髓性肌阵挛:一种罕见的颈椎病表现形式。
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