Diagnostic Challenges Posed by Preceding Peripheral Neuropathy in Very Late-onset Spinocerebellar Ataxia Type 3

被引:3
|
作者
Sugiyama, Atsuhiko [1 ]
Sekiguchi, Yukari [1 ]
Beppu, Minako [1 ,2 ]
Ishige, Takayuki [3 ]
Matsushita, Kazuyuki [3 ]
Kuwabara, Satoshi [1 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Neurol, Chiba, Japan
[2] Chiba Univ Hosp, Div Clin Genet, Chiba, Japan
[3] Chiba Univ Hosp, Div Lab Med, Chiba, Japan
基金
日本学术振兴会;
关键词
Machado-Joseph disease; neuronopathy; hot cross bun sign; magnetic resonance imaging; sensory ataxia; MACHADO-JOSEPH-DISEASE;
D O I
10.2169/internalmedicine.1382-18
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Peripheral neuropathy is a common extracerebellar manifestation of spinocerebellar ataxia type 3 (SCA3). However, to date, only a few SCA3 case reports have described the development of neuropathy before the emergence of apparent cerebellar signs. We herein report a case of very late-onset SCA3 in which preceding peripheral neuropathy seemingly concealed cerebellar signs, with seven years lapsing from the onset to the diagnosis. Horizontal gaze-evoked nystagmus and brain magnetic resonance imaging (MRI) findings prompted genetic testing, which confirmed the diagnosis of SCA3. A careful follow-up of neurological findings, such as nystagmus, and brain MRI are imperative for such cases.
引用
收藏
页码:119 / 122
页数:4
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