Purpose: To report a rare case of central vision loss in a patient with choroideremia.
Patients and methods: A retrospective, interventional case report.
Results: A 13-year-old male with history of choroideremia presented with subacute loss of central acuity in his left eye. Examination and diagnostic testing revealed subretinal fibrosis secondary to a choroidal neovascular membrane (CNVM). A trial of anti-vascular endothelial growth factor (VEGF) therapy with the injection of intravitreal bevacizumab was attempted. Mild improvements in acuity and anatomy were noted.
Conclusion: Choroideremia is a rare hereditary choroidal dystrophy that predominantly affects males in the first and second decades of life. Visual acuity is usually spared until later in life. CNVM is a rare manifestation of choroideremia with only a handful of case reports presented in the literature. This case is unique in that it is the first reported case that received treatment with intravitreal anti-VEGF therapy.
- Anti-VEGF therapy
- Chorioretinal degeneration
- Choroidal neovascular membrane
- Hereditary choroidal dystrophy
- Intravitreal bevacizumab injection
ASJC Scopus subject areas