| CASE REPORT |
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| Year : 2022 | Volume
: 36
| Issue : 4 | Page : 397-399 |
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How challenging can it be to treat Behçet uveitis?
Merih Oray, Zafer Cebeci, Nur Kir, Ilknur Tugal-Tutkun
Department of Ophthalmology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey
Correspondence Address:
Merih Oray
Istanbul Tip Fakultesi, Goz Hastaliklari A.D. 34390, Capa, Istanbul
Turkey
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/sjopt.sjopt_74_22
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A 20-year-old male Behçet uveitis (BU) patient presented with visual acuities (VAs) of hand movement in OD and counting fingers at 1 m in OS following treatment with corticosteroid monotherapy elsewhere. He had active intraocular inflammation OU along with macular hole and retinal detachment in OS. Infliximab (IFX) was started and vitreoretinal surgery was performed. He had infusion reaction with IFX, hepatotoxicity and depression with interferon, and resistance to adalimumab and tocilizumab therapies. Cytomegalovirus retinitis developed in OD following intravitreal dexamethasone implant and endophthalmitis developed in OS. At the 33rd month of follow-up, the patient was in clinical remission; however, there was persistent angiographic inflammation under certolizumab pegol, cyclosporine, mycophenolate mofetil, and low-dose prednisolone treatment. The left eye was phthisical and VA was 0.4 in OD. Immunomodulatory treatment is given based on the severity of inflammation in BU and needs to be closely monitored for efficacy and adverse effects.
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