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Recurrent Neuroretinitis: A Unique Presentation of Behçet's Disease in a Child
We describe a case of Behçet's disease (BD) in a young child that presented with recurrent neuroretinitis and developed retinal lesions during follow-up. A 4.5-year-old girl presented with fever of 39.5°C, erythema nodosum in her legs, bilateral knee arthritis, and perineum aphthae. On ocular e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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S. Karger AG
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588684/ https://www.ncbi.nlm.nih.gov/pubmed/33173499 http://dx.doi.org/10.1159/000509158 |
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author | Rabina, Gilad Amarilyo, Gil Zur, Dinah Harel, Liora Habot-Wilner, Zohar |
author_facet | Rabina, Gilad Amarilyo, Gil Zur, Dinah Harel, Liora Habot-Wilner, Zohar |
author_sort | Rabina, Gilad |
collection | PubMed |
description | We describe a case of Behçet's disease (BD) in a young child that presented with recurrent neuroretinitis and developed retinal lesions during follow-up. A 4.5-year-old girl presented with fever of 39.5°C, erythema nodosum in her legs, bilateral knee arthritis, and perineum aphthae. On ocular examination, visual acuity was 20/25 in both eyes. Right eye examination was normal and the left eye (LE) showed mild anterior and intermediate uveitis, normal optic disc, and a macular star appearance. Laboratory workup demonstrated elevated C-reactive protein levels, a normal abdominal ultrasound, and a normal colonoscopy. The patient was diagnosed with BD. One month post initial presentation, the patient presented with visual acuity of finger counting in the LE with significant anterior uveitis, mild intermediate uveitis, and recurrent neuroretinitis. Under treatment of IV methylprednisolone, oral betamethasone, infliximab, and colchicine, a complete systemic remission was noticed, and uveitis became quiescent. On last examination, 4.5 years post first presentation, visual acuity was 20/25 in both eyes and the LE demonstrated a remnant of a juxtafoveal retinal scar. To the best of our knowledge, this is the first case of neuroretinitis presenting as a manifestation of pediatric BD. Ophthalmologists should be aware of these unique manifestations of ocular BD. |
format | Online Article Text |
id | pubmed-7588684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-75886842020-11-09 Recurrent Neuroretinitis: A Unique Presentation of Behçet's Disease in a Child Rabina, Gilad Amarilyo, Gil Zur, Dinah Harel, Liora Habot-Wilner, Zohar Case Rep Ophthalmol Case Report We describe a case of Behçet's disease (BD) in a young child that presented with recurrent neuroretinitis and developed retinal lesions during follow-up. A 4.5-year-old girl presented with fever of 39.5°C, erythema nodosum in her legs, bilateral knee arthritis, and perineum aphthae. On ocular examination, visual acuity was 20/25 in both eyes. Right eye examination was normal and the left eye (LE) showed mild anterior and intermediate uveitis, normal optic disc, and a macular star appearance. Laboratory workup demonstrated elevated C-reactive protein levels, a normal abdominal ultrasound, and a normal colonoscopy. The patient was diagnosed with BD. One month post initial presentation, the patient presented with visual acuity of finger counting in the LE with significant anterior uveitis, mild intermediate uveitis, and recurrent neuroretinitis. Under treatment of IV methylprednisolone, oral betamethasone, infliximab, and colchicine, a complete systemic remission was noticed, and uveitis became quiescent. On last examination, 4.5 years post first presentation, visual acuity was 20/25 in both eyes and the LE demonstrated a remnant of a juxtafoveal retinal scar. To the best of our knowledge, this is the first case of neuroretinitis presenting as a manifestation of pediatric BD. Ophthalmologists should be aware of these unique manifestations of ocular BD. S. Karger AG 2020-10-08 /pmc/articles/PMC7588684/ /pubmed/33173499 http://dx.doi.org/10.1159/000509158 Text en Copyright © 2020 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Case Report Rabina, Gilad Amarilyo, Gil Zur, Dinah Harel, Liora Habot-Wilner, Zohar Recurrent Neuroretinitis: A Unique Presentation of Behçet's Disease in a Child |
title | Recurrent Neuroretinitis: A Unique Presentation of Behçet's Disease in a Child |
title_full | Recurrent Neuroretinitis: A Unique Presentation of Behçet's Disease in a Child |
title_fullStr | Recurrent Neuroretinitis: A Unique Presentation of Behçet's Disease in a Child |
title_full_unstemmed | Recurrent Neuroretinitis: A Unique Presentation of Behçet's Disease in a Child |
title_short | Recurrent Neuroretinitis: A Unique Presentation of Behçet's Disease in a Child |
title_sort | recurrent neuroretinitis: a unique presentation of behçet's disease in a child |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588684/ https://www.ncbi.nlm.nih.gov/pubmed/33173499 http://dx.doi.org/10.1159/000509158 |
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