From the Department of Neurology (A.S., S.K.), Graduate School of Medicine, Chiba University; Division of Dermatology (C.N., M.T.), Department of Internal Related, Kobe University, Graduate School of Medicine; and Department of Dermatology (Y.T.), Graduate School of Medicine, Chiba University, Japan.
Neurology. 2022 Oct 4;99(14):618-624. doi: 10.1212/WNL.0000000000201065. Epub 2022 Aug 2.
We describe the case of a 60-year-old man with a 16-year history of gait imbalance and a 15-year history of forgetfulness. The insidious onset and slow progression suggested that the disease was degenerative. Neurologic examination revealed cerebellar ataxia, chorea, and mild cognitive impairment. Brain MRI revealed prominent cerebellum atrophy and diffuse atrophy in the brainstem and cerebrum. Based on neurologic manifestations, an additional patient interview and skin examination were conducted. Photosensitivity and freckling in exposed areas, which the patient did not recognize as disease symptoms, were observed. Based on acute and chronic photosensitivity and DNA repair test results, a final diagnosis was made. In patients with cerebellar ataxia, chorea, and cognitive dysfunction of unknown etiology, clinicians should explore patients' history of photosensitivity and carefully examine the skin.
我们描述了一例 60 岁男性患者,其病史包括步态不稳 16 年和健忘 15 年。隐匿起病和缓慢进展提示疾病为退行性的。神经检查显示小脑共济失调、舞蹈病和轻度认知障碍。脑部 MRI 显示明显的小脑萎缩和脑干及大脑弥漫性萎缩。基于神经表现,我们对患者进行了额外的访谈和皮肤检查。观察到患者未意识到的光敏性和暴露部位的雀斑。基于急性和慢性光敏性以及 DNA 修复测试结果,做出了最终诊断。对于以小脑共济失调、舞蹈病和认知功能障碍为主要表现且病因不明的患者,临床医生应探索患者的光敏性病史,并仔细检查皮肤。