Juvenile temporal arteritis
Other Names for this Disease
- Juvenile giant cell arteritis
- Juvenile cranial arteritis
- Juvenile polymyalgia rheumatica
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vasculitis, a group of conditions that cause inflammation of the blood vessels. Unlike the classic form of temporal arteritis, this condition is generally diagnosed in late childhood or early adulthood and only affects the temporal arteries (located at the lower sides of the skull, directly underneath the temple). Affected people often have no signs or symptoms aside from a painless nodule or lump in the temporal region. The exact underlying cause of the condition is unknown. It generally occurs sporadically in people with no family history of the condition. Juvenile temporal arteritis is often treated with surgical excision and rarely recurs.Juvenile temporal arteritis is a rare form of
Last updated: 11/9/2015
- Kolman OK, Spinelli HM, Magro CM. Juvenile temporal arteritis. J Am Acad Dermatol. February 2010; 62(2):308-314.
- Juvenile temporal arteritis. Orphanet. January 2005; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=26137.
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- The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Juvenile temporal arteritis. Click on the link to view a sample search on this topic.