Latvala Heidi Madeleine, Reitan Solveig Klæbo, Vaaler Arne Einar
Department of Addiction, Division of Mental Health and Addiction, University Hospital of Northern Norway, Åsgårdvegen 40, 9016 Tromsø, Norway.
Department of Internal Medicine, Finnmark Hospital Trust, Sykehusveien 35, 9601 Hammerfest, Norway.
Case Rep Psychiatry. 2023 Feb 11;2023:7989712. doi: 10.1155/2023/7989712. eCollection 2023.
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. . 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.
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.
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。血管炎症可能导致动脉管腔狭窄,急性闭塞可能导致视力丧失和中风。典型症状包括头痛、发热和颌部间歇性运动障碍。然而,非典型表现越来越受到关注。我们报告一例70岁女性病例,除头痛和肌肉骨骼疼痛外,还伴有波动性躁狂症状和意识模糊。诊断为GCA后,使用皮质类固醇治疗使躯体症状逐渐改善。
皮质类固醇导致躁狂症状暂时加重,持续治疗3至4周后症状改善,表明这些症状很可能与GCA有关。据我们所知,该患者的临床表现和病程此前未被描述或报道过。因此,GCA在精神科人群中可能是一种诊断不足的疾病,在老年人出现非典型新发精神障碍时应予以考虑。