Erschienen in:
12.07.2023
Autoimmune Inflammatory Eye Disease: Demystifying Clinical Presentations for the Internist
verfasst von:
Richmond Woodward, Sri Meghana Konda, Dilraj S. Grewal
Erschienen in:
Current Allergy and Asthma Reports
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Ausgabe 8/2023
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Abstract
Purpose of Review
Provide a framework for recognizing key symptoms and clinical findings in patients with autoimmune inflammatory eye disease.
Recent Findings
The most common manifestations of autoimmune inflammatory eye disease are episcleritis, scleritis, uveitis (anterior, intermediate, posterior, and panuveitis), and keratoconjunctivitis sicca. Etiologies can be idiopathic or in association with a systemic autoimmune condition. Referral of patients who may have scleritis is critical for patients presenting with red eyes. Referral of patients who may have uveitis is critical for patients presenting often with floaters and vision complaints. Attention should also be directed to aspects of the history that might suggest a diagnosis of a systemic autoimmune condition, immunosuppression, drug-induced uveitis, or the possibility of a masquerade condition. Infectious etiologies should be ruled out in all cases.
Summary
Patients with autoimmune inflammatory eye disease may present with ocular or systemic symptoms alone, or in combination. Collaboration with ophthalmologists and other relevant specialists is vital to optimal long-term medical care.