Characteristics of Hirayama Disease in Young South Korean Soldiers.

IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Journal of Clinical Neurology Pub Date : 2024-05-01 Epub Date: 2024-02-05 DOI:10.3988/jcn.2023.0244
Jae-Hyun Yun, Chul Jung, Eun Jin Kim, Jaechan Park, Jiwoon Yeom, Ji Su Jung, Kyoung-Eun Kim
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Abstract

Background and purpose: The purpose of this study was to describe the clinical presentation and features in electrodiagnostic and imaging investigations of young South Korean males diagnosed with Hirayama disease (HD).

Methods: We reviewed the electronic medical records of South Korean enlisted soldiers who were diagnosed with HD and discharged from military service during 2011-2021. We investigated the clinical characteristics and results of electrodiagnostic and magnetic resonance imaging (MRI) investigations. We analyzed laterality and identified the involved muscles using needle electromyography (EMG). Loss of lordosis, localized cervical cord atrophy, loss of attachment between the posterior dura and subjacent lamina, asymmetric flattening of the cord, crescent-shaped mass in the posterior epidural space, and noncompressive intramedullary T2-weighted high signal intensity were investigated using neutral- or flexion-position MRI.

Results: Forty-two male patients aged 20.2±0.8 years (mean±standard deviation) were identified. All patients complained of hand weakness, and 10 complained of hand tremor (23.8%). Four patients (9.5%) had symptoms in both upper limbs, and five (11.9%) had sensory disturbances. Needle EMG revealed that muscles in the C7-T1 myotome were commonly involved, and C5-C6 involvement of the deltoid (10.5%) and biceps brachii (12.5%) was also observed. In cervical MRI, localized cord atrophy (90.0%) was the most characteristic finding, and cord atrophy was most severe at the C5-C6 level (58.3%).

Conclusions: This is the first description of a large number of patients with HD in South Korea. The clinical presentation and features found in electrodiagnostic and imaging investigations will improve the understanding of HD in the young South Korean male population.

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韩国年轻士兵平山症的特征:回顾性研究
背景与目的:本研究旨在描述被诊断为平山症(HD)的韩国年轻男性的临床表现以及电诊断和影像学检查的特征:我们查阅了 2011-2021 年间被诊断为 HD 并退伍的韩国入伍士兵的电子病历。我们调查了他们的临床特征以及电诊断和磁共振成像(MRI)检查结果。我们使用针式肌电图(EMG)分析了侧位并确定了受累肌肉。使用中立位或屈曲位核磁共振成像检查了颈椎前凸消失、局部颈脊髓萎缩、后硬膜与邻近薄层之间的附着丧失、脊髓不对称变平、硬膜外后间隙新月形肿块以及非压缩性髓内 T2 加权高信号强度:42例男性患者,年龄为(20.2±0.8)岁(平均值±标准差)。所有患者均主诉手部无力,10 名患者主诉手部震颤(23.8%)。四名患者(9.5%)双上肢均有症状,五名患者(11.9%)有感觉障碍。针刺肌电图(EMG)显示,C7-T1肌层肌肉普遍受累,C5-C6三角肌(10.5%)和肱二头肌(12.5%)也受累。在颈部核磁共振成像中,局部脊髓萎缩(90.0%)是最具特征性的发现,C5-C6水平的脊髓萎缩最为严重(58.3%):这是韩国首次对大量 HD 患者的描述。结论:这是首次对韩国大量 HD 患者的描述,其临床表现以及在电诊断和影像学检查中发现的特征将加深人们对韩国年轻男性 HD 患者的了解。
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来源期刊
Journal of Clinical Neurology
Journal of Clinical Neurology 医学-临床神经学
CiteScore
4.50
自引率
6.50%
发文量
0
审稿时长
>12 weeks
期刊介绍: The JCN aims to publish the cutting-edge research from around the world. The JCN covers clinical and translational research for physicians and researchers in the field of neurology. Encompassing the entire neurological diseases, our main focus is on the common disorders including stroke, epilepsy, Parkinson''s disease, dementia, multiple sclerosis, headache, and peripheral neuropathy. Any authors affiliated with an accredited biomedical institution may submit manuscripts of original articles, review articles, and letters to the editor. The JCN will allow clinical neurologists to enrich their knowledge of patient management, education, and clinical or experimental research, and hence their professionalism.
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