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Characteristics of Hirayama Disease in Young South Korean Soldiers
Jae-Hyun Yun1, Chul Jung1, Eun Jin Kim1
1Department of Rehabilitation Medicine, Armed Forces Capital Hospital, Seongnam, Korea.
Insights
Hirayama disease (HD) in young South Korean males often presents with hand weakness and tremor. Cervical MRI commonly shows cord atrophy, particularly at the C5-C6 level, aiding diagnosis.
Area of Science:
- Neurology
- Medical Imaging
- Electrophysiology
Background:
- Hirayama disease (HD) is a rare, self-limiting motor neuron disorder.
- Understanding its presentation in specific demographics is crucial for early diagnosis.
Purpose of the Study:
- To detail the clinical, electrodiagnostic, and imaging features of Hirayama disease in young South Korean males.
- To enhance diagnostic understanding within this population.
Main Methods:
- Retrospective review of medical records for South Korean enlisted soldiers diagnosed with HD (2011-2021).
- Analysis of clinical symptoms, needle electromyography (EMG), and cervical magnetic resonance imaging (MRI) findings.
- Specific MRI features investigated included cord atrophy, loss of lordosis, and dural attachment abnormalities.
Main Results:
- Forty-two male patients (mean age 20.2 years) were identified.
- Hand weakness was universal; tremor occurred in 23.8%.
- Cervical MRI revealed localized cord atrophy in 90%, most severe at C5-C6; EMG showed C7-T1 myotome involvement.
Conclusions:
- This study provides the first large-scale description of Hirayama disease in South Korea.
- The findings clarify the characteristic clinical and diagnostic features of HD in young South Korean males.
- Improved understanding aids in timely diagnosis and management of this condition.
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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