Severe Spinal Injury in Hirayama Disease

被引:2
|
作者
Quarracino, Cecilia [1 ]
Aguirre, Florencia [1 ]
Rugilo, Carlos A. [2 ]
De Negri, Luciana [1 ]
Villa, Andres M. [1 ]
机构
[1] Univ Buenos Aires, Ramos Med Hosp, Sch Med, Neurol Dept,Neuroimmunol & Electrophysiol Sect, Urquiza 609, RA-1211 Buenos Aires, DF, Argentina
[2] British Hosp Buenos Aires, Neuroradiol Sect, Buenos Aires, DF, Argentina
关键词
Hirayama disease; Oblique amyotrophy; Hand atrophy; Segmental spinal atrophy; Dynamic myelopathy;
D O I
10.4184/asj.2015.9.5.794
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Hirayama disease is a rare neurological disorder characterized by an insidious progressive subacute unilateral or bilateral weakness of the hands and forearm muscles leading to a painless amyotrophy. The disease primarily affects young men in the second to third decades of life. It has always been described as a second motor neuron disease, thus sparing the pyramidal and sensitive pathways. It usually has a slow progression course of 3 to 5 years followed by stabilization. Since its initial description by Keyzo Hirayama in 1959, most cases have been reported in Asia, particularly Japan and India, although the disease reportedly has worldwide distribution.
引用
收藏
页码:794 / 797
页数:4
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