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平山病:一种具有不寻常特征的罕见疾病。

Hirayama Disease: A Rare Disease with Unusual Features.

作者信息

Anuradha S, Fanai Vanlalmalsawmdawngliana

机构信息

Department of Medicine, Maulana Azad Medical College and Associated Hospitals, New Delhi 110002, India.

出版信息

Case Rep Neurol Med. 2016;2016:5839761. doi: 10.1155/2016/5839761. Epub 2016 Dec 21.

DOI:10.1155/2016/5839761
PMID:28097028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5209606/
Abstract

Hirayama disease, also known as monomelic amyotrophy (MMA), is a rare cervical myelopathy that manifests itself as a self-limited, asymmetrical, slowly progressive atrophic weakness of the forearms and hands predominantly in young males. The forward displacement of the posterior dura of the lower cervical dural canal during neck flexion has been postulated to lead to lower cervical cord atrophy with asymmetric flattening. We report a case of Hirayama disease in a 25-year-old Indian man presenting with gradually progressive asymmetrical weakness and wasting of both hands and forearms along with unusual features of autonomic dysfunction and upper motor neuron lesion.

摘要

平山病,也称为单肢肌萎缩症(MMA),是一种罕见的颈髓病,主要表现为年轻男性前臂和手部自限性、不对称、缓慢进展的萎缩性肌无力。颈部屈曲时下颈段硬脊膜管后硬膜向前移位被认为会导致下颈段脊髓萎缩并伴有不对称扁平。我们报告一例25岁印度男性平山病病例,该患者表现为双手和前臂逐渐进展的不对称肌无力和萎缩,同时伴有自主神经功能障碍和上运动神经元损害的异常特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41b2/5209606/6a672ff18d0f/CRINM2016-5839761.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41b2/5209606/f3e86717ef11/CRINM2016-5839761.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41b2/5209606/6a672ff18d0f/CRINM2016-5839761.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41b2/5209606/f3e86717ef11/CRINM2016-5839761.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41b2/5209606/6a672ff18d0f/CRINM2016-5839761.002.jpg

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本文引用的文献

1
Monomelic amyotrophy (hirayama disease) with upper motor neuron signs: a case report.伴有上运动神经元体征的单肢肌萎缩症(平山病):一例报告
Ann Rehabil Med. 2015 Feb;39(1):122-7. doi: 10.5535/arm.2015.39.1.122. Epub 2015 Feb 28.
2
Hirayama disease in a 17-year-old Chinese man.一名17岁中国男性的平山病
Singapore Med J. 2014 Jun;55(6):e87-9. doi: 10.11622/smedj.2013253.
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Nosology of juvenile muscular atrophy of distal upper extremity: from monomelic amyotrophy to Hirayama disease--Indian perspective.远端上肢少年性近端肌萎缩的分类学:从单一肢带肌萎缩到平山病——印度视角。
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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Somatosensory evoked potentials in Hirayama disease: A Brazilian study.平山病的体感诱发电位:一项巴西的研究。
Surg Neurol Int. 2020 Dec 22;11:464. doi: 10.25259/SNI_861_2020. eCollection 2020.
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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。
Asian J Neurosurg. 2020 May 29;15(2):405-408. doi: 10.4103/ajns.AJNS_291_19. eCollection 2020 Apr-Jun.
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Vietnamese Case Series of Hirayama Disease.越南平山病病例系列。
In Vivo. 2020 Jul-Aug;34(4):2153-2157. doi: 10.21873/invivo.12022.
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Is Hirayama a Gq1b disease?平山病是一种Gq1b疾病吗?
Neurol Sci. 2019 Aug;40(8):1743-1747. doi: 10.1007/s10072-019-03758-x. Epub 2019 Feb 23.
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Bilateral Upper Limb Weakness.双侧上肢无力。
Oman Med J. 2018 May;33(3):264-265. doi: 10.5001/omj.2018.49.
Biomed Res Int. 2013;2013:478516. doi: 10.1155/2013/478516. Epub 2013 Aug 26.
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Clinical and radiological profile of Hirayama disease: A flexion myelopathy due to tight cervical dural canal amenable to collar therapy.平山病的临床和影像学特征:一种因颈椎硬膜囊狭窄导致的屈颈型脊髓病,可采用颈托治疗。
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Biomechanical study of cervical flexion myelopathy using a three-dimensional finite element method.使用三维有限元方法对颈椎屈曲型脊髓病的生物力学研究
J Neurosurg Spine. 2008 May;8(5):436-41. doi: 10.3171/SPI/2008/8/5/436.
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Imaging features in Hirayama disease.平山病的影像学特征。
Neurol India. 2008 Jan-Mar;56(1):22-6. doi: 10.4103/0028-3886.39307.
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A case of Hirayama disease in Pakistan.
J Pak Med Assoc. 2007 Jan;57(1):41-4.
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Nationwide survey of juvenile muscular atrophy of distal upper extremity (Hirayama disease) in Japan.日本全国范围内青少年上肢远端型肌肉萎缩症(平山病)调查。
Amyotroph Lateral Scler. 2006 Mar;7(1):38-45. doi: 10.1080/14660820500396877.
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Neurology. 1963 May;13:373-80. doi: 10.1212/wnl.13.5.373.
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