Laser-Induced Photic Injury Phenocopies Macular Dystrophy

Lijuan Zhang, Andrew Zheng, Hongping Nie, Kavita V. Bhavsar, Yu Xu, David H. Sliney, Stephen L. Trokel, Stephen H. Tsang

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Objective: To describe the phenotypes associated with laser-induced retinal damage in children.Methods: Five patients with maculopathy and reduced visual acuity associated with laser pointer use were evaluated. Best-corrected visual acuity, retinal structure, and function were monitored with color fundus, infrared (IR), and red-free images, fundus autofluorescence (AF), spectral domain-optical coherence tomography (SD-OCT), and full-field electroretinography (ERG).Results: All five laser pointer injury patients had retinal lesions resembling a macular dystrophy (one bilateral and four unilateral). These lesions were irregular in shape but all had a characteristic dendritic appearance with linear streaks radiating from the lesion. Photoreceptor damage was present in all patients, but serial OCT monitoring showed that subsequent photoreceptor recovery occurred over time in the eyes of at least four patients. One patient also had bilateral pigment epithelial detachments (PED). Both hyper-and hypoautofluorecence were observed in the laser damage area.Conclusions: In general, OCT and IR images are quite useful to diagnose laser damage, but AF is not as sensitive. Laser pointer damage in children can occasionally be misdiagnosed as a macular dystrophy disease, but the distinctive lesions and OCT features are helpful for differentiating laser damage from other conditions.

Original languageEnglish (US)
Pages (from-to)59-67
Number of pages9
JournalOphthalmic Genetics
Volume37
Issue number1
DOIs
StatePublished - Jan 2 2016

Keywords

  • macular dystrophy
  • phenocopy
  • photic injury

ASJC Scopus subject areas

  • Ophthalmology
  • Pediatrics, Perinatology, and Child Health
  • Genetics(clinical)

Fingerprint

Dive into the research topics of 'Laser-Induced Photic Injury Phenocopies Macular Dystrophy'. Together they form a unique fingerprint.

Cite this