Suppr超能文献

精神障碍作为威尔逊病的首发临床症状——病例报告

Psychiatric disturbances as a first clinical symptom of Wilson's disease - case report.

作者信息

Litwin Tomasz, Dzieżyc Karolina, Karliński Michał, Szafrański Tomasz, Członkowska Anna

机构信息

II Klinika Neurologii IPiN w Warszawie.

Specjalistyczna Praktyka Lekarska Tomasz Szafrański, Warszawa.

出版信息

Psychiatr Pol. 2016;50(2):337-344. doi: 10.12740/PP/45218.

Abstract

OBJECTIVES

Wilson's disease (WD) is an inherited disorder of copper metabolism with wide spectrum of clinical symptoms, mainly hepatic or neurological. Psychiatric disorders occur less frequently and are not pathognomonic for WD. However, in almost 20% of cases they are in fact the first clinical manifestation of WD. The aim of this paper is to emphasise the importance of including WD in differential diagnosis of psychiatric disorders in young adults, as well as caution in initiating psychiatric treatment for patients with already established diagnosis of WD.

METHODS

Case report of a patient with primarily psychiatric manifestation of WD.

RESULTS

The authors present the case of a 26-year-old patient treated for 3 years due to depressive syndrome who was diagnosed as WD in the differential diagnosis shortly after extrapyramidal symptoms developed. During the further WD treatment the manic episode occurred. The patient was treated with atypical neuroleptics and anxiolytics, with good psychiatric effect, but with severe neurological deterioration. However, long term use of valproic acid and olanzapine combined with continuation of anti-copper treatment and rehabilitation resulted in good psychiatric and neurological outcome.

CONCLUSIONS

WD should be always considered in differential diagnosis of psychiatric disorders in young patients, especially if they present additional extrapyramidal or hepatic symptoms. It is also extremely important to remain cautious when drugs with high affinity to dopamine D2 receptors need to be initiated in patients already diagnosed with WD, as they may result in severe and often irreversible neurological complications.

摘要

目的

威尔逊病(WD)是一种遗传性铜代谢紊乱疾病,临床症状广泛,主要为肝脏或神经方面的症状。精神障碍较少见,并非WD的特征性表现。然而,在近20%的病例中,它们实际上是WD的首发临床表现。本文旨在强调在青年成人精神障碍鉴别诊断中纳入WD的重要性,以及对已确诊WD的患者启动精神治疗时需谨慎。

方法

报告一例以WD为主要精神表现的患者病例。

结果

作者介绍了一例26岁患者,因抑郁综合征接受治疗3年,在锥体外系症状出现后不久,在鉴别诊断中被诊断为WD。在进一步的WD治疗过程中出现了躁狂发作。患者接受非典型抗精神病药和抗焦虑药治疗,精神症状改善良好,但出现严重神经功能恶化。然而,长期使用丙戊酸和奥氮平并继续进行抗铜治疗及康复治疗,取得了良好的精神和神经方面的疗效。

结论

在年轻患者精神障碍的鉴别诊断中应始终考虑WD,尤其是当他们出现额外的锥体外系或肝脏症状时。对于已确诊WD的患者,在需要启动对多巴胺D2受体具有高亲和力的药物治疗时保持谨慎也极为重要,因为这些药物可能导致严重且往往不可逆的神经并发症。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验