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Updated: May 26, 2026

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Recent advances in diagnostic strategies for giant cell arteritis
Tanaz A Kermani1, Kenneth J Warrington
1Division of Rheumatology, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA. Kermani.Tanaz@mayo.edu
Insights
Giant cell arteritis (GCA) diagnosis relies on temporal artery biopsy. Advanced imaging aids GCA diagnosis, especially for large-vessel involvement when biopsy is negative, preventing irreversible vision loss.
Area of Science:
- Rheumatology
- Ophthalmology
- Vascular Medicine
Background:
- Giant cell arteritis (GCA) is a systemic vasculitis affecting major arteries.
- Ciliary artery involvement can cause irreversible ischemic optic neuropathy and blindness.
- Prompt glucocorticoid treatment is crucial to prevent vision loss, necessitating accurate diagnosis.
Purpose of the Study:
- To review diagnostic methods for Giant cell arteritis.
- To evaluate the role of imaging in GCA diagnosis.
- To highlight the limitations of current diagnostic tools.
Main Methods:
- Review of clinical features and laboratory findings in GCA.
- Discussion of histopathologic examination of the superficial temporal artery (TA).
- Evaluation of various imaging modalities for temporal artery assessment.
Main Results:
- Clinical and laboratory findings for GCA lack sensitivity and specificity.
- Temporal artery biopsy remains the gold standard for GCA diagnosis.
- Advanced imaging modalities show promise as adjuncts, particularly for large-vessel GCA.
Conclusions:
- Accurate diagnosis of GCA is essential due to the risks of prolonged glucocorticoid therapy.
- While TA biopsy is standard, noninvasive imaging offers valuable diagnostic support.
- Imaging advancements are improving GCA detection in cases with atypical presentations or negative biopsies.
Abstract:
Giant cell arteritis (GCA) is a systemic vasculitis that affects the aorta and its major branches. Involvement of the ciliary artery can result in ischemic optic neuropathy and subsequent blindness, which is typically irreversible. If GCA is suspected, treatment with glucocorticoids should be initiated promptly to prevent further vision loss. However, given the need for prolonged therapy with glucocorticoids and the morbidity associated with their use, diagnosis should be confirmed. Clinical features and laboratory findings are neither sensitive nor specific for GCA. The mainstay of diagnosis remains histopathologic examination of a section of the superficial temporal artery. Several imaging studies have been used to evaluate the temporal artery but, at present, their utility as alternatives to a temporal artery biopsy is limited. Recent advances in imaging modalities have allowed detailed noninvasive imaging of the large arteries and are a useful adjunct for the diagnosis of GCA, particularly in patients with primarily large-vessel involvement in whom temporal artery biopsy is often negative.
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