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Ghosh P et al. – Giant cell arteritis (GCA) is a vasculitis of large and medium–sized vessels that predominantly affects the elderly. GCA should be recognized as a medical emergency owing to its associated critical ischemia, which frequently causes neuro–ophthalmic complications. The pathogenesis of GCA is unclear, but it is speculated that the disease process is triggered by an infectious agent or an autoantigen (through molecular mimicry) being sensed by Toll–like receptors on immature dendritic cells in the tunica adventitia of arteries. Reparative processes then cause revascularization and intimal hyperplasia. This results in vascular occlusion and consequent tissue ischemia. Features predictive of visual loss in GCA include jaw claudication, diplopia and temporal artery abnormalities on physical examination. Modern imaging with duplex ultrasonography and fluorodeoxyglucose positron emission tomography shows promise for early diagnosis and detection of major artery involvement in GCA. However, temporal artery biopsy remains the gold–standard investigation. Early recognition and urgent institution of high–dose corticosteroids is the mainstay of treatment. Studies have found mixed experiences of using conventional disease–modifying drugs and biological therapies.

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