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以额叶为主的白质脑病伴精神分裂症样症状为先兆的威尔逊病

Wilson's Disease Preceded by Schizophrenia-like Symptoms with Frontal-dominant Leukoencephalopathy.

作者信息

Miyano Ryoji, Mitsutake Akihiko, Matsukawa Takashi, Obata Satomi, Koyama Hiroaki, Nakai Yudai, Ishiura Hiroyuki, Kubota Akatsuki, Shimizu Jun, Sakuishi Kaori, Toda Tatsushi

机构信息

Department of Neurology, Graduate School of Medicine, The University of Tokyo, Japan.

Department of Radiology, Graduate School of Medicine, The University of Tokyo, Japan.

出版信息

Intern Med. 2025 Jul 15;64(14):2240-2244. doi: 10.2169/internalmedicine.4353-24. Epub 2024 Dec 12.

Abstract

We herein report a 26-year-old man diagnosed with Wilson's disease (WD), initially treated for schizophrenia for 11 years. At 26 years old, he was admitted because of status epilepticus. Brain magnetic resonance imaging revealed frontal-dominant leukoencephalopathy with cystic changes and basal ganglia atrophy. The diagnosis of WD was confirmed based on neuropsychiatric symptoms, Kayser-Fleischer rings, abnormal copper metabolism, and a genetic analysis of ATP7B. Psychotic symptoms in WD can precede neurological manifestations, and extrapyramidal signs may be mistaken for drug-induced Parkinsonism. WD should be considered in patients presenting with progressive Parkinsonism preceded by schizophrenia-like psychiatric symptoms.

摘要

我们在此报告一名26岁男性,被诊断为威尔逊病(WD),最初因精神分裂症接受了11年的治疗。26岁时,他因癫痫持续状态入院。脑部磁共振成像显示以额叶为主的白质脑病伴囊性改变和基底节萎缩。基于神经精神症状、凯泽-弗莱舍尔环、铜代谢异常以及ATP7B基因分析,确诊为WD。WD的精神病性症状可能先于神经学表现出现,锥体外系体征可能被误诊为药物性帕金森综合征。对于出现类似精神分裂症的精神症状后继而出现进行性帕金森综合征的患者,应考虑WD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2e4/12331318/c48f4dca65a4/1349-7235-64-14-2240-g001.jpg

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