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非威尔逊氏肝豆状核变性:来自印度南部四个家族的临床与磁共振成像观察

Non-Wilsonian hepatolenticular degeneration: Clinical and MRI observations in four families from south India.

作者信息

Nagappa Madhu, Sinha Sanjib, Saini Jitender S, Kallolimath Pradeep, Singh Nivedita, Kumar Arun, Bindu Parayil S, Taly Arun B

机构信息

Department of Neurology, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bangalore 560 029, Karnataka, India.

Department of Neurology, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bangalore 560 029, Karnataka, India.

出版信息

J Clin Neurosci. 2016 May;27:91-4. doi: 10.1016/j.jocn.2015.06.035. Epub 2016 Jan 4.

Abstract

Non-Wilsonian hepatolenticular degeneration (NWHD) is a heterogeneous neurological disorder occurring secondary to chronic acquired liver disease. Genetically determined familial NWHD is rare, poorly understood, and often mistaken for Wilson's disease (WD). We analysed clinical and MRI profiles of NWHD patients who did not have obvious cause for acquired liver disease, such as alcohol intake or hepatitis. Six patients from four families (four males, two females, mean age: 17.0±standard deviation 7.9years), presenting with chronic extrapyramidal disorder resembling WD and imaging (abdominal ultrasound/MRI) evidence of cirrhosis were studied. They lacked Kayser-Fleischer rings or biochemical and/or genetic evidence of WD. Clinical features included dystonia (n=6), parkinsonism (n=3), tremor (n=1), cerebellar ataxia (n=3), orofacial dyskinesia (n=1), behavioural abnormalities (n=3), and cognitive decline (n=1). Brain MRI revealed T1-weighted hyperintensity in the pallidum (n=6), crus cerebri (n=4), putamen (n=1), caudate (n=1), thalamus (n=1), and red nucleus (n=1) with T2-weighted shortening in some of these regions. Additional findings included giant cisterna magna (n=1), face of giant panda sign (n=1) and thin corpus callosum (n=1). Areas of "blooming" on susceptibility weighted images were noted in two patients in the caudate (n=2) and putamen (n=1). The finding of T1 shortening is distinct from that of WD where the majority of lesions are T1-hypointense and T2-hyperintense. Extrapallidal T1-hyperintensity is also an exceptional observation in NWHD. The MRI appearance of intense T1 shortening coupled with the lack of increased susceptibility changes suggests that the most likely mineral deposited is manganese. The association of this neurological disorder and cirrhosis of the liver in the absence of an acquired liver disease is a distinct disease entity. This syndrome may represent a disorder of manganese metabolism resulting in its toxic deposition.

摘要

非威尔逊氏肝豆状核变性(NWHD)是一种继发于慢性获得性肝病的异质性神经系统疾病。基因决定的家族性NWHD较为罕见,了解甚少,且常被误诊为威尔逊氏病(WD)。我们分析了无明显获得性肝病病因(如饮酒或肝炎)的NWHD患者的临床和MRI特征。研究了来自四个家庭的六名患者(四名男性,两名女性,平均年龄:17.0±标准差7.9岁),他们表现出类似WD的慢性锥体外系疾病,且影像学检查(腹部超声/MRI)有肝硬化证据。他们没有凯泽-弗莱舍尔环或WD的生化和/或基因证据。临床特征包括肌张力障碍(n = 6)、帕金森症(n = 3)、震颤(n = 1)、小脑共济失调(n = 3)、口面部运动障碍(n = 1)、行为异常(n = 3)和认知衰退(n = 1)。脑部MRI显示苍白球(n = 6)、大脑脚(n = 4)、壳核(n = 1)、尾状核(n = 1)、丘脑(n = 1)和红核(n = 1)在T1加权像上呈高信号,其中一些区域T2加权像上信号缩短。其他发现包括巨大枕大池(n = 1)、大熊猫脸征(n = 1)和胼胝体变薄(n = 1)。两名患者在尾状核(n = 2)和壳核(n = 1)的磁敏感加权像上出现“ blooming”区域。T1缩短的表现与WD不同,WD的大多数病变在T1加权像上呈低信号,T2加权像上呈高信号。苍白球外T1高信号在NWHD中也是一个特殊表现。T1强烈缩短的MRI表现加上缺乏磁敏感变化增加提示最可能沉积的矿物质是锰。这种神经系统疾病与无获得性肝病的肝硬化的关联是一种独特的疾病实体。该综合征可能代表锰代谢紊乱导致其毒性沉积。

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