Finlayson M H, Superville B
Brain. 1981 Mar;104(Pt 1):79-95. doi: 10.1093/brain/104.1.79.
The brain lesions of our patients with chronic portal-systemic venous shunts were much the same regardless of the presence or absence of primary liver disease. Alzheimer's type 2 abnormality of astrocytes and demarcated areas of spongy degeneration were found, mainly in the grey matter, with more severe involvement of the basal ganglia and the deeper layers of the frontal, parietal and occipital cortex. The spongy degeneration showed an especially close correlation with the arterial blood supply, being greatest in borderland areas that fall between the regions usually supplied by one or other of the major cerebral arteries. Previous investigations have not been primarily concerned with selective vulnerability so that comparisons are difficult, but on review, there is evidence that this pattern of involvement is a feature of both Wilson's disease and acquired hepatocerebral degeneration. The toxic effect of the portal blood is greatest in the grey matter, probably because of the greater metabolic activity there, and the distribution of lesions within this area of greater vulnerability appears to be further influenced by circulatory factors.
无论是否存在原发性肝脏疾病,我们那些患有慢性门体静脉分流的患者的脑部病变大致相同。发现了星形胶质细胞的阿尔茨海默2型异常以及界限分明的海绵状变性区域,主要位于灰质中,基底神经节以及额叶、顶叶和枕叶皮质深层受累更为严重。海绵状变性与动脉血供显示出特别密切的相关性,在通常由一条或多条主要脑动脉供血区域之间的交界地带最为明显。先前的研究主要未关注选择性易损性,因此难以进行比较,但经审查发现,有证据表明这种受累模式是威尔逊病和后天性肝脑变性的特征。门脉血的毒性作用在灰质中最大,可能是因为那里的代谢活动更强,而在这个更易受损区域内病变的分布似乎进一步受到循环因素的影响。