Hepatic myelopathy

肝性脊髓病
  • 文章类型: Case Reports
    背景:肝性脊髓病是一种非常罕见的慢性肝病的神经系统并发症。患者习惯性出现进行性纯运动性痉挛性轻瘫。这种神经功能障碍几乎总是由于肝硬化和门腔分流,手术或自发。
    方法:我们报告了两例57岁的男性和37岁的女性患者,他们患有与肝硬化和门脉高压相关的进行性痉挛性轻瘫。这两名患者来自突尼斯(北非)。两名患者的脊髓磁共振成像正常,而脑磁共振成像显示苍白球的T2超信号。这些迹象,支持肝性脑病的两名肝硬化患者伴有孤立性进行性痉挛性轻瘫,无膀胱或感觉障碍,有助于保留肝性脊髓病的诊断。
    结论:肝性脊髓病是慢性肝病的一种严重且使人衰弱的神经系统并发症。发病机制被误解,似乎是多因素的,包括氨和其他致病性神经毒素的选择性神经毒性作用。通常有病理性脑磁共振成像显示肝性脑病,与有助于诊断肝性脊髓病的正常脊髓磁共振成像相反。保守治疗如降氨措施,饮食补充,抗痉挛药物,和血管内分流闭塞在改善疾病症状方面几乎没有益处。早期进行的肝移植可以防止疾病进展,并可能允许恢复。
    BACKGROUND: Hepatic myelopathy is a very rare neurological complication of chronic liver disease. Patients habitually present with progressive pure motor spastic paraparesis. This neurological dysfunction is almost always due to cirrhosis and portocaval shunt, either surgical or spontaneous.
    METHODS: We report two cases of a 57-year-old man and a 37-year-old woman with progressive spastic paraparesis linked to cirrhosis and portal hypertension. The two patients are of Tunisian origin (north Africa). Magnetic resonance imaging of the spinal cord of two patients was normal, while brain magnetic resonance imaging showed a T2 hypersignals of the pallidums. These signs, in favor of hepatic encephalopathy in the two patients with cirrhosis with isolated progressive spastic paraparesis without bladder or sensory disorders, help to retain the diagnosis of hepatic myelopathy.
    CONCLUSIONS: Hepatic myelopathy is a severe and debilitating neurological complication of chronic liver disease. The pathogenesis is misunderstood and seems to be multifactorial, including the selective neurotoxic role both of ammonia and other pathogenic neurotoxins. Usually a pathological brain magnetic resonance imaging showing a hepatic encephalopathy was documented, contrasting with a normal spinal cord magnetic resonance imaging that contributed to diagnosis of hepatic myelopathy. Conservative therapies such as ammonia-lowering measures, diet supplementation, antispastic drugs, and endovascular shunt occlusion show little benefit in improving disease symptoms. Liver transplantation performed at early stage can prevent disease progression and could probably allow for recovery.
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  • 文章类型: Case Reports
    肝性脊髓病(HM)是许多肝病晚期的罕见神经系统并发症,其特征是双侧痉挛性轻瘫,无感觉和括约肌功能障碍。它是由于与肝硬化相关的代谢紊乱和中枢神经系统功能障碍而发生的。没有及时有效的临床干预,这些患者的预后是毁灭性的。尽管肝移植(LT)是HM的有效治疗方法,这些患者的预后仍然不能令人满意.这种疾病的早期识别和诊断对于改善患者预后至关重要。这里,我们报告一例乙型肝炎病毒相关性失代偿性肝硬化合并HM。患者在LT后恢复良好。我们还总结了到2023年接受LT治疗的25例HM患者的临床特征和移植后结果,包括本例。
    Hepatic myelopathy (HM) is a rare neurological complication in the end stage of many liver diseases and is characterized by bilateral spastic paraparesis without sensory and sphincter dysfunction. It occurs owing to metabolic disorders and central nervous system dysfunction associated with cirrhosis. Without timely and effective clinical intervention, the prognosis of these patients is devastating. Although liver transplantation (LT) is an effective treatment for HM, the prognosis of these patients remains unsatisfactory. Early recognition and diagnosis of this disease are essential for improving patient prognosis. Here, we report a case of hepatitis B virus-associated decompensated cirrhosis with HM. The patient recovered well after LT. We also summarize the clinical characteristics and post-transplant outcomes of 25 patients with HM treated by LT through 2023, including this case.
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