巨细胞动脉炎表现为狂躁、精神病和认知功能障碍1例。

Q4 Medicine Case Reports in Psychiatry Pub Date : 2023-01-01 DOI:10.1155/2023/7989712
Heidi Madeleine Latvala, Solveig Klæbo Reitan, Arne Einar Vaaler
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引用次数: 0

摘要

背景:巨细胞动脉炎(GCA)是一种影响中、大动脉的自身免疫性血管炎。血管炎症可导致动脉腔狭窄,急性闭塞可导致视力丧失和中风。典型症状包括头痛、发热和下颌跛行。然而,越来越多的人认识到非典型的表现。案例演示。我们报告一个70岁的妇女的情况下,波动性躁狂症状和精神错乱,除了头痛和肌肉骨骼疼痛。诊断为GCA后,皮质类固醇治疗逐渐改善躯体症状。结论:皮质类固醇可导致躁狂症状暂时性加重,持续治疗3 ~ 4周后症状改善,提示症状极有可能与GCA有关。患者表现出临床特征和临床过程,据我们所知,以前没有描述或发表过。因此,GCA在精神病人群中可能是一种未被诊断的疾病,在老年非典型新发精神疾病的病例中应予以考虑。
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Giant Cell Arteritis Presenting with Mania, Psychosis, and Cognitive Dysfunction: A Case Report.

Background: Giant cell arteritis (GCA) is an autoimmune vasculitis affecting medium- and large-sized arteries. Vascular inflammation may lead to narrowing of the arterial lumen, and acute occlusion may result in vision loss and stroke. The classical symptoms include headache, fever, and jaw claudication. However, there is an increasing recognition of atypical presentations. Case Presentation. We report a case of a 70-year-old woman presenting with fluctuating manic symptoms and confusion, in addition to headache and musculoskeletal pain. After diagnosis of GCA, treatment with corticosteroids gradually improved the somatic symptoms.

Conclusion: Corticosteroids led to a temporary exacerbation of manic symptoms, which improved after 3 to 4 weeks of continuous treatment, indicating that the symptoms were most likely associated with GCA. The patient manifested with clinical features and a clinical course that has, to our knowledge, not been described or published before. Therefore, GCA may be an underdiagnosed disease in psychiatric populations and should be considered in case of atypical, new-onset psychiatric disorders in the elderly.

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来源期刊
Case Reports in Psychiatry
Case Reports in Psychiatry Medicine-Psychiatry and Mental Health
CiteScore
1.00
自引率
0.00%
发文量
49
审稿时长
12 weeks
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