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Published on: February 8, 2019
Correlations between histopathological findings and clinical manifestations in biopsy-proven giant cell arteritis
Francesco Muratore1, Luigi Boiardi1, Alberto Cavazza2
1Rheumatology Unit, Department of Internal Medicine, Azienda Ospedaliera ASMN, Istituto di Ricovero e Cura a Carattere Scientifico, Reggio Emilia, Italy.
Insights
Temporal artery biopsy (TAB) findings can predict giant cell arteritis (GCA) complications. Histopathological features like giant cells and calcifications correlate with cranial ischemic events and visual loss, aiding patient management.
Area of Science:
- Rheumatology
- Pathology
- Vascular Medicine
Background:
- Giant cell arteritis (GCA) is a systemic vasculitis affecting large and medium arteries.
- Temporal artery biopsy (TAB) is a key diagnostic tool for GCA.
- Understanding the correlation between TAB histopathology and clinical outcomes is crucial for patient management.
Purpose of the Study:
- To investigate the association between histopathological features identified in temporal artery biopsies (TABs) and the clinical manifestations of giant cell arteritis (GCA).
- To identify specific pathological findings in TAB that predict adverse outcomes in patients with biopsy-proven GCA.
Main Methods:
- A retrospective analysis of temporal artery biopsies (TABs) from patients with biopsy-proven GCA was conducted.
- Histopathological features including inflammation severity, intimal hyperplasia, thrombosis, calcifications, giant cells, and necrosis were evaluated by a blinded pathologist.
- Clinical data, including cranial ischemic events (CIEs) and visual manifestations, were correlated with TAB findings.
Main Results:
- In 274 patients with GCA, cranial ischemic events (CIEs) occurred in 58.8% and permanent visual loss in 18.6%.
- Predictors for CIEs included older age, lower ESR, presence of giant cells, and laminar necrosis on TAB.
- Predictors for permanent visual loss included lower CRP and the presence of calcifications on TAB.
Conclusions:
- Histopathological features observed in temporal artery biopsies (TABs) can predict specific clinical manifestations of giant cell arteritis (GCA).
- Findings such as giant cells, laminar necrosis, and calcifications are associated with increased risk of CIEs and visual loss.
- These correlations have potential implications for tailoring patient management strategies in GCA.
Objective:
To correlate histopathological features of positive temporal artery biopsy (TAB) and clinical manifestations of the disease in a large single-center population-based cohort of patients with biopsy-proven giant cell arteritis (GCA).
Methods:
A pathologist with expertise in vasculitis and blinded to clinical data and final diagnosis reviewed all TABs performed for suspected GCA at our hospital between January 1986 and December 2013. Histopathologic features evaluated were: the severity of inflammation and intimal hyperplasia, both graded on a semiquantitative scale (mild = 1, moderate = 2, severe = 3), the presence of intraluminal acute thrombosis, calcifications, giant cells, fibrinoid necrosis and laminar necrosis.
Results:
274 patients had a final diagnosis of biopsy-proven GCA and were included in the study. Cranial ischemic events (CIEs) were observed in 161 (58.8%), visual manifestations in 79 (28.8%) and permanent (partial or complete) visual loss in 51 (18.6%) patients. Predictors for the development of CIEs were older age (OR = 1.057, 95% CI 1.019-1.097, p = 0.003), lower ESR values (OR = 0.990, 95% CI 0.981-0.999, p = 0.026) as well as the presence of giant cells (OR = 1.848, 95% CI 1.045-3.269, p = 0.035) and laminar necrosis at TAB (OR = 2.334, 95% CI 1.187-4.587, p = 0.014). Predictors for the development of permanent visual loss were lower CRP values (OR = 0.906, 95% CI 0.827-0.992, p = 0.033) and the presence of calcifications at TAB (OR = 3.672, 95% CI 1.479-9.121, p = 0.005). Fibrinoid necrosis was not observed in any of the TABs evaluated.
Conclusion:
Pathological features of TAB may predict some manifestations of GCA. These findings may have implications for patients' management.
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