Retinal vascular abnormality of non-perfusion and neovascularization in a toddler with neurofibromatosis type 1.

Retin Cases Brief Rep

Department of Ophthalmology, Eye Diseases and Optometry Institute, Peking University People's Hospital, Beijing, China.

Published: October 2024

Purpose: This report describes the case of a 13-month-old boy diagnosed with neurofibromatosis type 1, who presented with retinal vascular abnormalities including extensive non-perfusion and neovascularization. We also discuss the observed changes following photocoagulation treatment.

Methods: A 13-month-old boy presented to the Department of Ophthalmology at Peking University People's Hospital with a reduction in the width of the left palpebral fissure for the past 6 months.

Results: The boy exhibited more than six café-au-lait spots larger than 5 mm in diameter on his trunk and legs. Fundus examination of the left eye revealed significant neovascularization in the temporal periphery of the retina, with late leakage and non-perfusion also noted temporally in fluorescein angiography (FA). Magnetic resonance imaging of the brain and orbits showed an enlarged left sphenoid body, a widened left cavernous sinus, and a large plexiform neurofibroma. Laser treatment was performed on the left eye. Five months later, the neovascularization was controlled.

Conclusion: Careful fundus examinations and systemic reviews, especially FA, are essential. Timely laser treatment is crucial for controlling disease progression and preventing retinal detachment.

Download full-text PDF

Source
http://dx.doi.org/10.1097/ICB.0000000000001673DOI Listing

Publication Analysis

Top Keywords

retinal vascular
8
non-perfusion neovascularization
8
neurofibromatosis type
8
13-month-old boy
8
left eye
8
laser treatment
8
left
5
vascular abnormality
4
abnormality non-perfusion
4
neovascularization
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!