Atypical Mid-Late Phase ICGA Hyperfluorescence in a Secondary MEWDS Case: A Distinct Disease or a Shift in Our Understanding of MEWDS?
This case describes an unusual secondary MEWDS presentation with unique imaging findings. The peculiar ICGA behavior and evolving FAF patterns may suggest either a distinct disease or a shift in our understanding of MEWDS involving photoreceptoritis, early RPE dysfunction, followed by more advanced RPE damage. The findings underscore the need for a nuanced approach to interpreting white-dot syndromes.
Authors
- Yoo-Ri Chung (ORCID: https://orcid.org/0000-0002-6871-6721)
- Sara Touhami (ORCID: https://orcid.org/0000-0001-8346-3067)
- Bahram Bodaghi (ORCID: https://orcid.org/0000-0002-0962-5301)
- Maria Vittoria Cicinelli
- Francesc March
- Victoria Konikowski
Institutions
- Vita-Salute San Raffaele University (IT)
- Universitat de Girona (ES)
- Sorbonne Université (FR)
- Istituti di Ricovero e Cura a Carattere Scientifico (IT)
- Hôpital Tenon (FR)
- Istituto di Ricovero e Cura a Carattere Scientifico San Raffaele (IT)
- Ajou University (KR)
Publication Details
- Journal
- Ocular Immunology and Inflammation
- Published
- 2025-04-17
- DOI
- https://doi.org/10.1080/09273948.2025.2493363
- Citations
- 2
- Primary Topic
- Cardiac tumors and thrombi
- Type
- article
- Field-Weighted Citation Impact
- 2.78