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平山病伴发颈椎畸形和脊髓压迫:来自瑞典的病例报告。

Hirayama's disease associated with cervical deformity and spinal cord compression: a case report from Sweden.

机构信息

Department of Surgical and Perioperative Sciences, Umeå University, Orthopaedics, Umeå, Sweden.

Division of Neuroradiology, Umeå University, Umeå, Sweden.

出版信息

Acta Neurochir (Wien). 2024 Feb 10;166(1):75. doi: 10.1007/s00701-024-05982-7.

DOI:10.1007/s00701-024-05982-7
PMID:38337063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10858154/
Abstract

BACKGROUND

Hirayama's disease (HD) is most common in young males, and previous studies are predominantly from Asian countries. The cause of HD is unknown but the most common theory about the pathology speculates on forward bending that causes a compression of the dura mater and the anterior horn of the spinal cord against the vertebra during an overstretch flexion that may result in myelopathy. Both anterior and posterior cervical surgical approaches have been shown to be effective in stopping the disease and improving function; however, HD is also reported to be a self-limited disease, and treatment with a cervical collar may be an alternative for these patients.

CASE REPORT

We report HD in a 17-year-old male from Sweden who underwent surgical treatment with a 2 level anterior cervical discectomy and fusion (ACDF) due to neurological progression from HD after conservative treatment.

CONCLUSION

HD is rare and is easily overlooked. Surgical intervention shows promising results for neurological progression, but HD is also reported to be a self-limited disease.

摘要

背景

平山病(HD)最常见于年轻男性,以往的研究主要来自亚洲国家。HD 的病因不明,但最常见的病理理论推测是向前弯曲导致硬脑膜和脊髓前角在过度伸展弯曲时被压缩在脊椎上,可能导致脊髓病。前后颈椎手术入路均已被证明可有效阻止疾病进展并改善功能;然而,HD 也被报道为一种自限性疾病,对于这些患者,颈托治疗可能是一种替代方法。

病例报告

我们报告了一例来自瑞典的 17 岁男性 HD 病例,该患者在保守治疗后因 HD 出现神经进展而行 2 节段前路颈椎间盘切除术和融合术(ACDF)。

结论

HD 较为罕见,容易被忽视。手术干预对神经进展显示出有前景的结果,但 HD 也被报道为一种自限性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/242e/10858154/70068dbbbe01/701_2024_5982_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/242e/10858154/4e7059d9c44c/701_2024_5982_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/242e/10858154/5d37deaf8d7f/701_2024_5982_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/242e/10858154/70068dbbbe01/701_2024_5982_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/242e/10858154/4e7059d9c44c/701_2024_5982_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/242e/10858154/5d37deaf8d7f/701_2024_5982_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/242e/10858154/70068dbbbe01/701_2024_5982_Fig3_HTML.jpg

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Hirayama's disease associated with cervical deformity and spinal cord compression: a case report from Sweden.平山病伴发颈椎畸形和脊髓压迫:来自瑞典的病例报告。
Acta Neurochir (Wien). 2024 Feb 10;166(1):75. doi: 10.1007/s00701-024-05982-7.
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本文引用的文献

1
Do patients with Hirayama disease require surgical treatment? A review of the literature.平山病患者需要手术治疗吗?文献综述。
Intractable Rare Dis Res. 2022 Nov;11(4):173-179. doi: 10.5582/irdr.2022.01105.
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Surgical treatment of spinal cord compression due to Hirayama disease: illustrative case.平山病所致脊髓压迫症的外科治疗:病例展示
J Neurosurg Case Lessons. 2022 Mar 7;3(10). doi: 10.3171/CASE21697.
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Juvenile muscular atrophy of the distal upper extremity (Hirayama syndrome): a systematic review.青少年上肢远端肌肉萎缩(平山病):一项系统综述
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Update on the Pathogenesis, Clinical Diagnosis, and Treatment of Hirayama Disease.平山病的发病机制、临床诊断及治疗进展
Front Neurol. 2022 Feb 1;12:811943. doi: 10.3389/fneur.2021.811943. eCollection 2021.
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Impact of various cervical surgical interventions in patients with Hirayama's disease-a narrative review and meta-analysis.不同颈椎手术干预对平山病患者的影响:一项叙述性综述和荟萃分析。
Neurosurg Rev. 2021 Dec;44(6):3229-3247. doi: 10.1007/s10143-021-01540-2. Epub 2021 Apr 21.
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Surgical Management of Hirayama Disease: A Rare Entity with Unusual Clinical Features.平山病的外科治疗:一种具有不寻常临床特征的罕见疾病。
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Hirayama disease.平山病
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C5 Palsy After Cervical Spine Surgery: A Multicenter Retrospective Review of 59 Cases.颈椎手术后的C5麻痹:59例多中心回顾性研究
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[Investigation of the compliance of cervical collar therapy in 73 patients with Hirayama disease].73例平山病患者颈托治疗依从性的调查
Zhonghua Yi Xue Za Zhi. 2016 Nov 22;96(43):3485-3488. doi: 10.3760/cma.j.issn.0376-2491.2016.43.009.