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Giant Cell Arteritis Fumiaki Suzuki 1 , Kazumi Kimura 1 1Department of Neurology, Nippon Medical School Keyword: 巨細胞性動脈炎 , 側頭動脈炎 , giant cell arteritis , GCA , cranial-GCA , large vessel-GCA , temporal arteritis , cranial GCA , large-vessel GCA pp.496-502
Published Date 2021/5/1
DOI https://doi.org/10.11477/mf.1416201791
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Abstract

Giant cell arteritis (GCA), also referred to as temporal arteritis, is a variant of large-vessel vasculitis. GCA should be considered in the differential diagnosis in patients aged >50 years, who present with headache, abrupt onset of visual disturbances, unexplained fever, a high erythrocyte sedimentation rate, and high serum C-reactive protein levels. Diagnosis of GCA is based on accurate interpretation of laboratory data, temporal artery biopsy findings, and imaging study results. Imaging modalities used for GCA include positron emission tomography, computed tomography (CT), CT angiography, and conventional magnetic resonance angiography. Biopsy is the gold standard for diagnosis of GCA. Glucocorticoids (GCs) are used as standard treatment to induce remission and also for maintenance therapy. However, clinicians should be aware of the adverse effects of GC treatment, including hyperglycemia, an immunocompromised state, and delirium. If adverse effects outweigh the benefits of GC treatment, it is necessary to consider switching to or adding an immunosuppressant to the therapeutic regimen.


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電子版ISSN 1344-8129 印刷版ISSN 1881-6096 医学書院

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