Professional Documents
Culture Documents
• 2 main forms:
Giant Cell Arteritis (GCA)
Almost always >50y
Takayasu Arteritis (TAK)
Almost always <50y
• Pathophysiology
Activation of adventitial dendritic cells, recruitment of CD4+ T-
lymphocytes and infiltration of macrophages, resulting in cytokine
driven neovascularisation and intimal hyperplasia. (2)
Giant Cell Arteritis
About
• Immune-mediated, ischaemic condition, caused by inflammation in the wall of
medium to large arteries
• 2-3:1 (F:M), Caucasians
• Risk of permanent vision loss, large vessel stenosis, aortic aneurysm
Presentation/Assessment
• Headache
• Systemic symptoms – fever, anorexia, fatigue
• 15% patients with PUO will have GCA
• Visual disturbances
• Raised CRP
Giant Cell Arteritis
Management
• Rheumatology review/advice
• Prednisone
• Consider temporal artery biopsy
• Histology: inflammation of inner media and intima;
granulomas
• Low dose aspirin
• PPI (omeprazole)
• Regular follow-up
References
1. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855435/
2. https://journals.sagepub.com/doi/10.1177/1358863X18802989
3. Health pathways