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首页> 外文期刊>Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology >Long-term clinical and radiological improvement of chronic acquired hepatocerebral degeneration after obliteration of portosystemic shunt: Report of a case
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Long-term clinical and radiological improvement of chronic acquired hepatocerebral degeneration after obliteration of portosystemic shunt: Report of a case

机译:闭门分流术后慢性获得性肝脑变性的长期临床和放射学改善:病例报告

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摘要

Neurological manifestations are common in patients with decompensated cirrhosis. The majority of these patients show hepatic encephalopathy or chronic acquired (non-Wilsonian) hepatocerebral degeneration (CAHD). They characteristically present with dysarthria, ataxia, involuntary movements, and altered mental status. Neuroradiological examination in patients with hepatic encephalopathy often shows abnormal signals in multiple regions of the brain, such as the pallidum, putamen, caudate nucleus, hemispheric white matter, and ventral midbrain. The pathogenesis of hepatic encephalopathy and CAHD is poorly understood and the response to conventional therapies is often poor. We report a male patient with cirrhosis of unknown cause, who developed slowly progressive cerebellar truncal and limb ataxia and slurred speech. Magnetic resonance imaging (MRI) showed focal T2 hyperintensity in bilateral dentate nuclei and middle cerebellar peduncles (MCPs). After treatment by obliteration of the portosystemic shunt, clinical manifestations and MRI abnormalities were dramatically improved. He was followed for six years until he died of uncontrollable bleeding due to hepatocellular carcinoma. At the last examination 9 months before death, he showed no apparent aggravation of neurological symptoms, and no abnormal signal intensities in the MCPs and supratentorial compartment. The clinical course and changes of brain MRI findings of this case are extremely rare, suggesting that obliteration of the portosystemic shunt may be effective for CAHD over long term.
机译:神经失调在肝硬化失代偿患者中很常见。这些患者中大多数显示出肝性脑病或慢性获得性(非Wilsonian)肝脑变性(CAHD)。他们典型地表现为构音障碍,共济失调,非自愿运动和精神状态改变。肝性脑病患者的神经放射学检查通常会在大脑的多个区域显示异常信号,例如苍白球,壳核,尾状核,半球白质和腹中脑。肝性脑病和CAHD的发病机理了解甚少,对传统疗法的反应通常较差。我们报告了一位原因不明的肝硬化男性患者,该患者发展缓慢进行性小脑截肢和四肢共济失调,言语不清。磁共振成像(MRI)显示双侧齿状核和中小脑梗(MCPs)出现局灶性T2高信号。通过闭门系统分流器治疗后,临床表现和MRI异常得到了显着改善。他被追踪了六年,直到因肝细胞癌无法控制的出血而死亡。在死亡前9个月的最后一次检查中,他没有出现明显的神经系统症状加重,并且在MCP和上睑腔室中没有异常的信号强度。这种情况的临床过程和脑部MRI表现的改变极为罕见,这表明长期消除门体分流可能对CAHD有效。

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