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

机译:在非常迟发的3型脊髓小脑共济失调之前的周围神经病变所带来的诊断挑战

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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.
机译:周围神经病变是3型脊髓小脑共济失调的常见小脑外表现。但是,迄今为止,只有少数SCA3病例报告描述了在明显的小脑体征出现之前神经病变的发展。我们在这里报告了一个非常迟发的SCA3病例,其中先前的周围神经病似乎掩盖了小脑体征,从发病到诊断已经过去了7年。水平凝视诱发的眼球震颤和脑磁共振成像(MRI)的发现促使进行了基因检测,从而证实了SCA3的诊断。对于此类病例,必须认真随访眼球震颤等神经系统发现和脑部MRI。

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