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威尔逊病的特征性神经放射学征象——事实还是虚构?

Pathognomonic neuroradiological signs in Wilson's disease - Truth or myth?

作者信息

Rędzia-Ogrodnik Barbara, Członkowska Anna, Antos Agnieszka, Bembenek Jan, Kurkowska-Jastrzębska Iwona, Przybyłkowski Adam, Skowrońska Marta, Smoliński Łukasz, Litwin Tomasz

机构信息

Department of Radiology, Institute of Psychiatry and Neurology, Warsaw, Poland.

Second Department of Neurology, Institute of Psychiatry and Neurology, Warsaw, Poland.

出版信息

Parkinsonism Relat Disord. 2023 Feb;107:105247. doi: 10.1016/j.parkreldis.2022.105247. Epub 2022 Dec 17.

Abstract

INTRODUCTION

Wilson's disease (WD) is a treatable genetic disorder caused by impaired copper metabolism. Early diagnosis and correct anti-copper treatment are crucial for therapeutic success. Brain magnetic resonance imaging (MRI) is used both for diagnosis and treatment monitoring. Several neuroradiological signs have been proposed to be pathognomonic for WD; however, their frequency and significance are not established. The frequency and significance of these brain MRI signs were analyzed in a large cohort of WD patients.

METHODS

We retrospectively analyzed 100 newly diagnosed, treatment-naive WD patients. Brain MRI was performed and the frequency of typical MRI changes was analyzed with demographic, clinical and laboratory characteristics of WD.

RESULTS

Potentially pathognomonic brain MRI signs for WD occurred in 24% patients and in 43% (24/55) patients with neurological WD. Signs detected included the "face of the giant panda" in 15% of all patients (27.3% of neurological cases), "miniature panda" in 12% (21.8% of neurological cases), "split thalamus" in 7% (12.7% of neurological cases), and "bright claustrum" and "whorl" signs in 1 patients each. Signs were observed only in patients with neurological symptoms and were significantly associated with early age of onset/diagnosis, more severe neurological presentation and lower ceruloplasmin level (all p < 0.05).

CONCLUSIONS

Potentially brain MRI pathognomonic signs occurred relatively rarely across all patients, most often in patients with early onset and severe neurological symptoms, and this knowledge may improve WD diagnosis. However, as these signs are also found in brain MRI in other disorders, they may not be truly pathognomonic of WD.

摘要

引言

威尔逊病(WD)是一种可治疗的遗传性疾病,由铜代谢受损引起。早期诊断和正确的抗铜治疗对于治疗成功至关重要。脑磁共振成像(MRI)用于诊断和治疗监测。已提出几种神经放射学征象可作为WD的特征性表现;然而,它们的出现频率和意义尚未确定。在一大群WD患者中分析了这些脑MRI征象的频率和意义。

方法

我们回顾性分析了100例新诊断的、未接受过治疗的WD患者。进行了脑MRI检查,并分析了典型MRI变化的频率与WD的人口统计学、临床和实验室特征之间的关系。

结果

24%的患者出现了可能为WD特征性的脑MRI征象,在43%(24/55)有神经系统症状的WD患者中出现。检测到的征象包括:15%的所有患者(27.3%的神经系统病例)出现“大熊猫脸”,12%(21.8%的神经系统病例)出现“小熊猫”,7%(12.7%的神经系统病例)出现“丘脑分离”,各有1例患者出现“屏状核明亮”和“漩涡”征象。这些征象仅在有神经系统症状的患者中观察到,且与发病/诊断年龄早、神经系统表现更严重和铜蓝蛋白水平较低显著相关(所有p<0.05)。

结论

在所有患者中,可能具有特征性的脑MRI征象相对少见,最常出现在发病早且有严重神经系统症状的患者中,这一认识可能有助于WD的诊断。然而,由于这些征象也可见于其他疾病的脑MRI中,它们可能并非WD真正的特征性表现。

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