Format

Send to:

Choose Destination
See comment in PubMed Commons below
Rheumatol Int. 2008 Nov;29(1):1-7. doi: 10.1007/s00296-008-0662-0. Epub 2008 Aug 21.

Giant cell arteritis.

Author information

  • 1Department of Neurology, The Second Xiangya Hospital, Central South University, Changsha, China. higherwx@163.com

Abstract

Giant cell arteritis (GCA) is an immune-mediated chronic vasculitis of large- and medium-sized vessels usually occurring in White individuals aged over 50 years, in Western countries. The pathological hallmark of GCA is granulomatous inflammation of the involved vessels. Headache of new-onset is the most common clinical manifestation, and permanent vision loss is the most feared complication of GCA. The level of clinical suspicion for GCA should be based upon patient age, clinical symptoms, laboratory evaluation, and imaging findings. However, the diagnostic gold standard is achieved by histologic confirmation by temporal artery biopsy. Corticosteroids remain the only proven treatment for GCA and the prognosis for visual recovery is poor.

PMID:
18716781
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Springer
    Loading ...
    Write to the Help Desk