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A Case Report of Pediatric-Onset Ms Associated Uveitis Publisher



Mahdizad Z1 ; Zarei M1 ; Fakhredin H1, 5 ; Samiee R2 ; Heidari H3 ; Ebrahimiadib N4
Authors
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Authors Affiliations
  1. 1. Ophthalmology Department, Retina Service, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Student`S Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Multiple Sclerosis Research Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Ophthalmology Department, Ocular Immunology and Uveitis Foundation, Waltham, MA, United States
  5. 5. Retina & amp
  6. 6. Vitreous Service, Farabi Comprehensive Center of Excellence in Ophthalmology, Qazvin Square, Tehran, 1336616351, Iran

Source: Journal of Ophthalmic Inflammation and Infection Published:2024


Abstract

Background: To report a case of Pediatric-onset MS associated uveitis managed with local and systemic medications. Case presentation: An 11-year-old boy who was diagnosed with Pediatric-onset MS (POMS) with the first presentation of left optic neuritis in another center, was referred to our clinic with the complaint of non-improved vision in the left eye despite receiving IV 5gr methylprednisolone. After the ophthalmologic examinations, the patient was diagnosed as bilateral POMS-associated intermediate uveitis, and local treatment with corticosteroid was administered to both eyes. He was continued on systemic therapy such as Rituximab and five sessions of plasmapheresis. After four months, the patient's vision improved from FC at 50cm to 9/10 in the left eye. The intensity of intraocular inflammation decreased in both eyes. In fluorescein angiography findings, the optic disc, as well as vascular leakage, subsided bilaterally. Conclusion: Despite its rarity, POMS-associated uveitis presents a considerable challenge that necessitates the collaborative efforts of neurologists and ophthalmologists to achieve the most effective treatment outcomes. © The Author(s) 2024.