Cranial involvement in giant cell arteritis

被引:3
作者
Bosch, Philipp [1 ]
Espigol-Frigole, Georgina [2 ]
Cid, Maria C. [2 ]
Mollan, Susan P. [3 ,4 ]
Schmidt, Wolfgang A. [5 ]
机构
[1] Med Univ Graz, Dept Rheumatol & Immunol, A-8036 Graz, Austria
[2] Univ Barcelona, Inst Invest Biomed August Pi I Sunyer, Hosp Clin, Dept Autoimmune Dis, Barcelona, Spain
[3] Univ Hosp Birmingham NHS Fdn Trust, Birmingham Neuroophthalmol, Birmingham, England
[4] Univ Birmingham, Inst Metab & Syst Res, Translat Brain Sci, Birmingham, England
[5] Immanuel Hosp Berlin, Med Ctr Rheumatol Berlin Buch, Dept Rheumatol, Berlin, Germany
关键词
COLOR DOPPLER SONOGRAPHY; ACUTE MIDDLE MACULOPATHY; POLYMYALGIA-RHEUMATICA; AMERICAN-COLLEGE; DOUBLE-BLIND; DIAGNOSTIC-ACCURACY; SERUM MARKERS; FOLLOW-UP; TOCILIZUMAB; CLASSIFICATION;
D O I
10.1016/S2665-9913(24)00024-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Since its first clinical description in 1890, extensive research has advanced our understanding of giant cell arteritis, leading to improvements in both diagnosis and management for affected patients. Imaging studies have shown that the disease frequently extends beyond the typical cranial arteries, also affecting large vessels such as the aorta and its proximal branches. Meanwhile, advances in comprehending the underlying pathophysiology of giant cell arteritis have given rise to numerous potential therapeutic agents, which aim to minimise the need for glucocorticoid treatment and prevent flares. Classification criteria for giant cell arteritis, as well as recommendations for management, imaging, and treat-to-target have been developed or updated in the last 5 years, and current research encompasses a broad spectrum covering basic, translational, and clinical research. In this Series paper, we aim to discuss the current understanding of giant cell arteritis with cranial manifestations, describe the clinical approach to this condition, and explore future directions in research and patient care.
引用
收藏
页码:e384 / e396
页数:13
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