Kuwabara K, Hitoshi S, Nukina N, Ishii K, Momose T, Kubota S, Seyama Y, Kanazawa I
Department of Neurology, Faculty of Medicine, University of Tokyo, Japan.
J Neurol Sci. 1996 Jun;138(1-2):145-9. doi: 10.1016/0022-510x(96)00011-1.
We describe a 34-year-old Japanese woman presenting gait difficulty and Achilles tendon swelling. The patient was diagnosed as having cerebrotendinous xanthomatosis (CTX) based on the high serum cholestanol level and diminished enzymatic activity of 27-hydroxylase of fibroblasts from her skin. Her clinical presentation was atypical regarding the presence of hemiparkinsonism and absence of apparent cataract, dementia, and cerebellar ataxia. Although MRI studies could not detect any abnormality in the basal ganglia or midbrain, PET analysis using [18F]-6-fluoro-L-dopa revealed reduced uptake of dopamine into the putamen, suggesting the impairment of presynaptic dopaminergic neurons.
我们描述了一名34岁的日本女性,她出现步态困难和跟腱肿胀。基于高血清胆甾烷醇水平以及其皮肤成纤维细胞中27-羟化酶的酶活性降低,该患者被诊断为患有脑腱性黄瘤病(CTX)。就其存在偏侧帕金森症以及没有明显的白内障、痴呆和小脑共济失调而言,她的临床表现并不典型。尽管MRI研究未在基底神经节或中脑检测到任何异常,但使用[¹⁸F]-6-氟-L-多巴的PET分析显示壳核中多巴胺摄取减少,提示突触前多巴胺能神经元受损。