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Neuro-ophthalmic sarcoidosis
Robert P Baughman1, Kenneth L Weiss2, Karl C Golnik3
1Department of Medicine.
Eye and Brain
|May 26, 2017
Summary
Neuro-ophthalmic sarcoidosis affects one-third of patients, commonly involving the optic nerve. Treatment includes systemic therapy, often starting with corticosteroids, with steroid-sparing agents and TNF inhibitors for chronic or refractory cases.
Area of Science:
- Ophthalmology
- Neurology
- Immunology
Background:
- Neurosarcoidosis frequently impacts the visual system, with optic nerve involvement being the most common presentation.
- Differential diagnosis is crucial, as other conditions like multiple sclerosis can mimic neuro-ophthalmic sarcoidosis.
- Sarcoidosis diagnosis relies on identifying its multi-organ involvement and specific diagnostic tests.
Purpose of the Study:
- To summarize the key aspects of neuro-ophthalmic sarcoidosis, including its manifestations, diagnosis, and treatment strategies.
Main Methods:
- Review of existing literature on neuro-ophthalmic sarcoidosis.
- Analysis of common clinical presentations and diagnostic criteria.
- Evaluation of therapeutic approaches, including corticosteroids, cytotoxic agents, and biologic therapies.
Main Results:
- Approximately one-third of neurosarcoidosis patients experience neuro-ophthalmic disease.
- Optic nerve compromise is the most frequent ocular manifestation.
- Systemic therapy is generally required, with corticosteroids as first-line treatment.
Conclusions:
- Neuro-ophthalmic sarcoidosis necessitates systemic treatment, often involving a stepwise approach.
- Steroid-sparing agents like methotrexate and azathioprine are valuable for managing chronic disease.
- Tumor necrosis factor inhibitors show promise for refractory neuro-ophthalmic sarcoidosis.
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