Abstract
Giant cell arteritis (GCA) is a systemic granulomatous vasculitis of unknown etiology that typically involves the branches of the carotid artery (the temporal artery, in particular). However, it may affect any medium- or large-sized artery which makes establishment of its diagnosis even more difficult [1]. As early as in the tenth century, the famous Arabian physician Ali ibn Isa recommended removal of the temporal artery in order to treat migraine in patients with a simultaneous chronic eye disease often terminating in loss of sight [2]. From the clinical point of view, temporal arteritis was for the first time described by Hutchinson in 1890; the histopathological features related to the clinical syndrome were outlined by Horton in 1932, but it was as late as in 1938 that Jennings recognized that blindness might be a severe complication of the disease [3]. Later Gilmour, a pathologist, found out that temporal arteritis could involve also other arteries, and he was the first to use the term “giant cell arteritis.”
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Rovenský, J., Kozák, I. (2017). Giant Cell Arteritis, Polymyalgia Rheumatica, and Ocular Involvement. In: Rovenský, J., Leeb, B., Štvrtinová, V., Imrich, R. (eds) Polymyalgia Rheumatica and Giant Cell Arteritis. Springer, Cham. https://doi.org/10.1007/978-3-319-52222-7_16
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