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Published on: February 8, 2019
Giant cell arteritis: A rare cause of posterior vasculitis
Marilita M Moschos1, Yan Guex-Crosier
1Department of Ophthalmology, University of Athens, Greece. moschosmarilita@yahoo.fr
Insights
Giant cell arteritis (GCA) can cause posterior vasculitis, a condition affecting vision. Prompt diagnosis and treatment with systemic prednisolone are crucial for resolution.
Area of Science:
- Ophthalmology
- Rheumatology
- Vascular Medicine
Background:
- Giant cell arteritis (GCA) is a systemic vasculitis primarily affecting large and medium-sized arteries.
- Posterior segment ocular involvement in GCA, though less common than anterior segment, can lead to significant visual impairment.
Observation:
- This report details three cases of subacute GCA presenting with posterior vasculitis.
- Patients exhibited decreased vision, confirmed by ophthalmologic examination and fluorescein angiography.
- Laboratory findings included elevated erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) levels.
Findings:
- Temporal artery biopsy confirmed the diagnosis of GCA in all three patients.
- Posterior vasculitis was the primary ocular manifestation in these cases.
- Systemic prednisolone therapy led to resolution of symptoms and inflammatory markers.
Implications:
- GCA should be considered in the differential diagnosis of posterior vasculitis, especially with elevated ESR and CRP.
- Early recognition and treatment of GCA are vital to prevent irreversible vision loss.
- This highlights the importance of a comprehensive ophthalmologic evaluation in suspected GCA cases.
Purpose:
To report three cases of posterior vasculitis associated with subacute giant cell arteritis (GCA).
Methods:
Three patients with decreased vision underwent complete ophthalmologic examination and fluorescein angiography.
Results:
All patients presented posterior vasculitis. Patient 1 had an erythrocyte sedimentation rate (ESR) of 38 mm/hr and a C-reactive protein (CRP) of 28mg/L. Patient 2 and 3 had an ESR of 104 and 95 mm/hr and a CRP of 42 and 195 mg/L accordingly. Diagnosis was established by temporal artery biopsy. Resolution was observed after systemic prednisolone therapy.
Conclusion:
GCA should be suspected when posterior vasculitis and relatively high ESR and CRP are present.
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