Evaluation of neurologically symptomatic and asymptomatic patients in childhood Wilson's disease with central nervous system involvement: A retrospective observational study

A. M. Res, G. Yucel, S. Gungor
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Abstract

Abstract Objective: The aim was to evaluate the clinical and laboratory characteristics of children with Wilson's disease (WD) with and without neurological presentation with abnormalities on brain magnetic resonance imaging (MRI) and to describe the relationship of these observations with disease severity and functional outcome and their impact on prognosis. Materials and methods: Demographic, neuropsychiatric findings, laboratory, disease severity and functional results of 48 children with neurologically symptomatic and asymptomatic WD were evaluated retrospectively. Results: A significant positive correlation was found between the neurologic symptom score and functional outcome in WD with neurological presentation (p <0.001). A significant positive correlation was found between disease severity scores (PELD, MELD, Child Pugh and Dhwin score) and modified Rankin scores (mRS) in WD without neurological presentation (p <0.001, 0.004, <0.001, 0.001, respectively). In addition, a significant positive correlation was found between total bilirubin, direct bilirubin and Internationel Normalized Ratio (INR) values and mRS scores (p= 0.006, 0.012, 0.004, respectively). Kayser-Fleischer Ring sign in the eye was higher in the group with neurological symtomatic WD (p <0.001). The number of patients presenting with clinic of fulminant hepatitis and hepatic encephalopathy was significantly higher in the neurological asymptomatic group (p <0.001) Conclusion: Brain MRI changes may occur even in hepatic WD and presymptomatic cases, although infrequently, regardless of the presence of neurological symptoms. It should be known that neurological symptoms in children and adolescents may occur without significant liver disease. Even without neurological symptoms, all children with WD should have a brain MRI before treatment.
儿童威尔森氏病累及中枢神经系统的神经系统症状和无症状患者的评估:一项回顾性观察研究
摘要目的:评价有或无神经学表现伴脑磁共振成像(MRI)异常的威尔逊氏病(WD)患儿的临床和实验室特征,并描述这些观察结果与疾病严重程度和功能结局的关系及其对预后的影响。材料和方法:回顾性分析48例有神经症状和无症状WD患儿的人口学、神经精神病学表现、实验室、疾病严重程度和功能结果。结果:伴有神经症状表现的WD患者神经症状评分与功能结局呈正相关(p <0.001)。无神经症状的WD患者疾病严重程度评分(PELD、MELD、Child Pugh和Dhwin评分)与改良Rankin评分(mRS)呈显著正相关(p分别<0.001、0.004、<0.001、0.001)。总胆红素、直接胆红素、国际标准化比值(INR)值与mRS评分呈显著正相关(p分别为0.006、0.012、0.004)。伴有神经系统症状的WD组的Kayser-Fleischer Ring征象较高(p <0.001)。临床表现为暴发性肝炎和肝性脑病的患者数量在无神经症状组中明显高于无神经症状组(p <0.001)。结论:即使在肝性WD和症状前病例中也可能发生脑MRI改变,尽管不常见,但与有无神经症状无关。应该知道,儿童和青少年的神经症状可能没有明显的肝脏疾病。即使没有神经系统症状,所有患有WD的儿童在治疗前都应该进行脑部MRI检查。
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