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平山病——一例罕见病例报告并文献复习

Hirayama's Disease - A Rare Case Report with Review of Literature.

作者信息

Narayana Gowda B S, Mohan Kumar J, Basim Praveen Kumar

机构信息

Dr Narayana Gowda BS PES Medical College, Kuppam, Chittore, Andra Pradesh.

出版信息

J Orthop Case Rep. 2013 Jul-Sep;3(3):11-4. doi: 10.13107/jocr.2250-0685.107.

Abstract

INTRODUCTION

Hirayama's disease is a rare benign disorder, also referred to as monomelic amyotrophy (MMA), Juvenile non progressive amyotrophy, Sobue disease. It is a focal, lower motor neuron type of disease. Mainly young males in their second and third decades of age are most commonly affected. It is seen most commonly in Asian countries like India and Japan. In majority of people cause of this disease is unknown. MRI of cervical spine in flexion will reveal the cardinal features of Hirayama disease.

CASE REPORT

A 22 year gentleman came with a history of insidious onset of weakness in both the hands begenning with left side followed by right of 4 years duration. On examination he had clawing of both hands with wasting of forearm muscles. Lower limbs had no abnormality with normal deep tendon reflexes. MRI showed thinning of cord from C4 to C7 level suggestive of cord atrophy. Based on these features a diagnosis of focal amyotrophy was made. A cervical collar was prescribed and patient is under regular follow up.

CONCLUSION

Hirayama disease is a rare self-limiting disease. Early diagnosis is necessary as the use of a simple cervical collar which will prevent neck flexion, has been shown to stop the progression.

摘要

引言

平山病是一种罕见的良性疾病,也被称为单肢肌萎缩症(MMA)、青少年非进行性肌萎缩症、宗藤病。它是一种局灶性的下运动神经元疾病。主要在20至30岁的年轻男性中最为常见。在印度和日本等亚洲国家最为多见。大多数患者病因不明。颈椎屈曲位磁共振成像(MRI)可显示平山病的主要特征。

病例报告

一名22岁男性患者,双手渐进性无力4年,起病隐匿,先从左侧开始,随后累及右侧。检查发现双手呈爪形,前臂肌肉萎缩。双下肢无异常,深腱反射正常。MRI显示颈4至颈7节段脊髓变细,提示脊髓萎缩。基于这些特征,诊断为局灶性肌萎缩症。给予佩戴颈托,患者定期随访。

结论

平山病是一种罕见的自限性疾病。早期诊断很有必要,因为使用简单的颈托可防止颈部屈曲,已证明能阻止病情进展。

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