Giant cell arteritis and scleritis: A rare association
1Department of Internal Medicine, University Hospital of Strasbourg, 1 porte de l'hôpital, 67000 Strasbourg, France.
Caspian Journal of Internal Medicine
|August 17, 2022
Summary
Giant cell arteritis (GCA) can cause scleritis, an eye inflammation. Tocilizumab, an anti-IL6 therapy, is a promising treatment for GCA-related scleritis, especially when corticosteroids are ineffective.
Area of Science:
- Ophthalmology
- Rheumatology
- Immunology
Background:
- Giant cell arteritis (GCA) is a large-vessel vasculitis affecting the elderly, often causing ischemic complications.
- Ocular involvement in GCA typically manifests as anterior ischemic optic neuropathy, leading to irreversible vision loss.
- Scleritis is a rare but significant ocular manifestation of GCA.
Observation:
- A patient with GCA presented with recurrent isolated scleritis (anterior and posterior, unilateral and bilateral) despite corticosteroid therapy.
- The patient exhibited corticosteroid dependence and resistance to methotrexate.
- Tocilizumab, an anti-IL6 biologic, was initiated due to treatment resistance.
Findings:
- Recurrent scleritis in GCA can occur independently of other systemic inflammatory markers.
- Corticosteroid dependence and methotrexate resistance present a therapeutic challenge in managing GCA-associated scleritis.
- Tocilizumab demonstrated potential efficacy in managing refractory GCA-related scleritis.
Implications:
- This case highlights the importance of considering scleritis in GCA, even without other overt signs of inflammation.
- Tocilizumab represents a viable therapeutic option for refractory GCA-associated scleritis.
- Further research is warranted to establish treatment guidelines for GCA-related scleritis, particularly concerning biologic therapies.
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