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威尔逊氏病:一项临床神经病理学尸检研究。

Wilson's disease: a clinico-neuropathological autopsy study.

作者信息

Meenakshi-Sundaram S, Mahadevan A, Taly A B, Arunodaya G R, Swamy H S, Shankar S K

机构信息

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, India.

出版信息

J Clin Neurosci. 2008 Apr;15(4):409-17. doi: 10.1016/j.jocn.2006.07.017. Epub 2008 Jan 31.

Abstract

Wilson's disease (WD), a familial neurological disorder involving the brain and liver secondary to altered copper metabolism, is common in South India. In view of the paucity of studies on this condition, the pathomorphological features of eight cases of WD were studied in detail at autopsy (brain alone, 1; brain and liver biopsy, 1; brain and visceral organs, 6), and are described with a discussion of the differential features of the neurological and hepatic forms. Of the six patients presenting with neurological manifestations, five had central pontine myelinolysis, five had subcortical white matter cavitations, four had putaminal softening, and six had variable ventricular dilatation, unlike the hepatic form. The presence of Opalski cells and pontine myelinolysis appear to be specific to the neurological form of WD. Liver abnormalities were observed in all cases (cirrhosis, 6; steatosis, 4; chronic active hepatitis, 2). Contrary to the rubric 'hepatolenticular degeneration', involvement of the lenticular nucleus was not universal, and nor was the pathology restricted to these anatomical areas.

摘要

威尔逊氏病(WD)是一种因铜代谢改变继发累及脑和肝脏的家族性神经疾病,在印度南部较为常见。鉴于针对该病症的研究较少,我们对8例WD病例的病理形态学特征进行了详细尸检研究(仅脑,1例;脑和肝脏活检,1例;脑和内脏器官,6例),并在文中描述了其特征,同时讨论了神经型和肝型的鉴别特征。与肝型不同,在6例出现神经症状的患者中,5例有中央桥脑髓鞘溶解,5例有皮质下白质空洞,4例有壳核软化,6例有不同程度的脑室扩张。奥帕尔斯基细胞的存在和桥脑髓鞘溶解似乎是WD神经型所特有的。所有病例均观察到肝脏异常(肝硬化,6例;脂肪变性,第4例;慢性活动性肝炎,2例)。与“肝豆状核变性”这一名称相反,豆状核受累并不普遍,且病理改变也不限于这些解剖区域。

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