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[一例86岁起病的舞蹈症-棘红细胞增多症病例]

[A case of chorea-acanthocytosis onset with at age 86].

作者信息

Ikawa Masamichi, Yoneda Makoto, Kuriyama Masaru

机构信息

Second Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui.

出版信息

Rinsho Shinkeigaku. 2005 Aug;45(8):603-6.

Abstract

An 86-year-old woman was admitted to our hospital for orobuccolingual dyskinesia. She did not take any medication. Her relatives had no similar symptoms nor consanguineous marriage. Although orobuccolingual dyskinesia was improved by administration of haloperidol for a while, orobuccolingual dyskinesia with biting of tongue and lips, chorea and muscular atrophy in the legs, seizures and dementia appeared half a year after the onset. The decrease of cMAP suggested axonopathy in the extremities by a nerve conduction study. The serum level of CK was normal. The EEG showed generally slow wave activities. A head MRI showed mild atrophy of the bilateral caudate nuclei and frontal lobes with scattered old lacunars in the deep white matter. She was diagnosed as having chorea-acanthocytosis (ChAc) because acanthocytes (10-20%) appeared in the peripheral blood. The normal lipoprotein levels and Kell antigen expression excluded the possibilities of Bassen-Kornzweig syndrome and McLeod syndrome. In all reported cases of ChAc, she was the oldest onset patient. ChAc is warranted in a patient presenting with orobuccolingual dyskinesia with biting, in spite of elderly onset.

摘要

一名86岁女性因口颊舌运动障碍入住我院。她未服用任何药物。其亲属无类似症状,也没有近亲结婚情况。尽管使用氟哌啶醇治疗一段时间后口颊舌运动障碍有所改善,但发病半年后出现了伴有咬舌和咬唇的口颊舌运动障碍、腿部舞蹈症和肌肉萎缩、癫痫发作及痴呆。神经传导研究显示复合肌肉动作电位(cMAP)降低提示肢体轴索性神经病。肌酸激酶(CK)血清水平正常。脑电图显示普遍慢波活动。头部磁共振成像(MRI)显示双侧尾状核和额叶轻度萎缩,深部白质有散在陈旧性腔隙。由于外周血中出现棘形红细胞(10% - 20%),她被诊断为舞蹈症 - 棘红细胞增多症(ChAc)。正常的脂蛋白水平和凯尔抗原表达排除了巴森 - 科尔茨韦格综合征和麦克劳德综合征的可能性。在所有已报道的ChAc病例中,她是发病年龄最大的患者。对于出现伴有咬症的口颊舌运动障碍的患者,尽管发病年龄较大,也有必要考虑ChAc。

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