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Peripapillary pachychoroid neovasculopathy: A novel entity
Javier Montero Hernández1, Lidia Remolí Sargues1, Clara Monferrer Adsuara1
1Department of Ophthalmology, Consorcio Hospital General Universitario of Valencia, Valencia, Spain.
Peripapillary pachychoroid neovasculopathy is a newly identified condition within pachychoroid spectrum disease. This case report details its features and successful treatment, advancing understanding of choroidal neovascularization.
Area of Science:
- Ophthalmology
- Medical Imaging
- Pathology
Background:
- Pachychoroid disease spectrum is a group of conditions characterized by choroidal thickening.
- Peripapillary pachychoroid syndrome is a recently described variant.
- Understanding its pathogenic mechanisms and association with neovascularization is crucial.
Observation:
- A 51-year-old woman presented with macular pigmentary changes.
- Spectral-domain optical coherence tomography revealed pigment epithelium detachment and pachyvessels.
- Optical coherence tomography angiography demonstrated extensive neovascularization.
Findings:
- Diagnosis of peripapillary pachychoroid neovasculopathy was established.
- Indocyanine green angiography confirmed pachyvessels and choroidal hyper-permeability.
- Intravitreal aflibercept treatment led to favorable visual and anatomical outcomes.
Implications:
- This case contributes to defining peripapillary pachychoroid neovasculopathy as a distinct entity.
- It enhances comprehension of choroidal neovascularization pathogenesis in pachychoroid disorders.
- It highlights effective treatment strategies for this condition.
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