Painful ophthalmoplaegia secondary to orbital myositis.

To cite: Hoffman J, Fayers T. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015210106 DESCRIPTION A 53-year-old man with rheumatoid arthritis presented with 1 week of progressive right-sided proptosis, diplopia and pain on eye movement, particularly when looking to the left. Examination demonstrated marked lid swelling, limited right elevation and dextroelevation with pain on adduction (figure 1A). The affected eye was injected and chemosed. There was no evidence of optic nerve compromise. The patient was started on intravenous antibiotics for presumed orbital cellulitis. CT scan demonstrated thickening of the right lateral and superior rectus muscles and their tendinous insertions (figure 2). The patient was diagnosed with orbital myositis and treated with 80 mg oral prednisolone. His symptoms improved almost immediately and 24 h later his ophthalmoplaegia and diplopia had resolved (figure 1B). He was discharged on a reducing corticosteroid regime. Orbital myositis typically presents with painful diplopia. Pain is often worst when looking in the opposite direction to the action of the affected muscles, that is, when the muscle is stretched. It forms part of the idiopathic orbital inflammatory disease spectrum and is associated with systemic inflammatory diseases such as rheumatoid arthritis, sarcoidosis, Crohn’s disease, systemic lupus erythematous and antineutrophil cytoplasmic antibody-associated vasculitis. The aetiology is unknown but recent research suggests an association with IgG4. Differential diagnoses include orbital cellulitis, orbital neoplasm, carotid– cavernous fistulae, arteriovenous malformations and thyroid eye disease. Since it can mimic orbital cellulitis, intravenous antibiotics are often started empirically; the lack of response may raise the suspicion of an alternative diagnosis. In contrast to orbital cellulitis, there is no fever, and white cell count and inflammatory markers are normal. CT/MRI is very useful to aid diagnosis. Treatment with high-dose corticosteroids usually produces a dramatic response. It can recur and refractory cases may require treatment with immunosuppressant drugs or radiotherapy.