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Recurrent Neuroretinitis: A Unique Presentation of Behçet's Disease in a Child
Gilad Rabina1, Gil Amarilyo2, Dinah Zur1
1Department of Ophthalmology, Tel Aviv Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Insights
This case study highlights neuroretinitis as a rare manifestation of pediatric Behçet's disease (BD). Early diagnosis and comprehensive treatment are crucial for managing ocular symptoms and preventing vision loss in children with BD.
Area of Science:
- Ophthalmology
- Rheumatology
- Pediatrics
Background:
- Behçet's disease (BD) is a rare multisystemic inflammatory disorder.
- Ocular involvement is common in BD, but neuroretinitis is an uncommon presentation, especially in pediatric cases.
Observation:
- A 4.5-year-old girl with fever, erythema nodosum, arthritis, and aphthae was diagnosed with BD.
- She presented with recurrent neuroretinitis and macular star appearance in the left eye.
- Ocular findings included anterior and intermediate uveitis, progressing to significant vision loss.
Findings:
- The patient received treatment with IV methylprednisolone, oral betamethasone, infliximab, and colchicine.
- Systemic remission and quiescent uveitis were achieved.
- Long-term follow-up revealed a remnant juxtafoveal retinal scar but preserved visual acuity.
Implications:
- This is the first reported case of neuroretinitis as a manifestation of pediatric BD.
- Ophthalmologists should consider BD in the differential diagnosis of neuroretinitis in children.
- Prompt diagnosis and multidisciplinary management are essential for favorable visual outcomes in pediatric BD with ocular involvement.
Abstract:
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.
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