Abstract
Purpose: To describe myopic nontractional foveal detachment associated with pachychoroid diseases. Methods: This retrospective study included 15 myopic eyes which had nontractional serous foveal detachment. The eyes were divided into myopic central serous chorioretinopathy (CSC) group (n = 8) and a myopic pachychoroid neovascularization (PNV) group (n = 7) according to the presence of type 1 choroidal neovascularization on multimodal imaging. The findings of multimodal imaging and treatment response were described. Results: In myopic CSC group, pachychoroid features such as pachyvessels, choroidal vascular hyperpermeability and punctate hyperfluorescent spots were noted in 8 eyes (100%), 8 eyes (100%), 5 eyes (62.5%) respectively. The above features were noted in 7 eyes (100%), 5 eyes (83.3%), 5 eyes (83.3%), respectively, in the myopic PNV group. Five of 8 eyes in myopic CSC and all 7 eyes received treatment including anti-vascular endothelial growth factor injection and/or photodynamic therapy. However, only five eyes had a complete response. Conclusions: The pachychoroid phenotype may coexist with high myopia and lead to myopic nontractional serous foveal detachment. Our series suggest that the response to treatment for these conditions would be limited.
| Original language | English |
|---|---|
| Article number | 288 |
| Journal | BMC Ophthalmology |
| Volume | 21 |
| Issue number | 1 |
| DOIs | |
| State | Published - Dec 2021 |
| Externally published | Yes |
Keywords
- Central serous chorioretinopathy
- Myopia
- Myopic nontractional foveal detachment
- Pachychoroid neovascularization
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