Purpose: To evaluate multifocal evanescent white dot syndrome (MEWDS) patients with and without overlapping multifocal choroiditis (MFC).

Methods: Thirty-four patients diagnosed between November 2008 and August 2018 at 2 hospitals were retrospectively reviewed. Multimodal imaging including optical coherence tomography angiography (OCTA) was assessed.

Results: Twenty-seven (79%) patients were women (overall mean age, 30 years). Five developed MFC lesions in the affected eyes, and one developed MFC in the unaffected fellow eye. Another developed combined MEWDS and MFC in the fellow eye during follow-up. Eyes with MFC had thicker choroids (316.5 and 197.3 µm, respectively; = .001) at presentation, which became thinner after resolution ( = .043). Those with subfoveal MFC had poor visual prognosis ( = .019). Areas of suspected choriocapillaris flow deficit were identified on OCTA.

Conclusion: Some MEWDS patients may develop overlapping MFC in the same or fellow eyes, presenting with increased choroidal thickness which decreased after resolution.

Download full-text PDF

Source
http://dx.doi.org/10.1080/09273948.2020.1795206DOI Listing

Publication Analysis

Top Keywords

evanescent white
8
white dot
8
dot syndrome
8
overlapping multifocal
8
multifocal choroiditis
8
mewds patients
8
developed mfc
8
fellow eye
8
mfc fellow
8
mfc
6

Similar Publications

Stage 1 Extensive Macular Atrophy with Pseudodrusen-Like Appearance Complicated by Multiple Evanescent White Dot Syndrome-Like Reaction.

Ocul Immunol Inflamm

December 2024

Harvard Retinal Imaging Lab, Retina Service, Department of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.

Purpose: To describe a case of early-stage Extensive Macular Atrophy with Pseudodrusen-like appearance (EMAP) presenting with acute monocular loss and atypical retinal lesions suggestive of posterior uveitis.

Methods: Case report with longitudinal follow-up including visual field testing and multimodal imaging.

Results: A 53-year-old woman presented with sudden vision loss in her right eye (RE).

View Article and Find Full Text PDF

An update of multimodal imaging in white dot syndrome.

Oman J Ophthalmol

October 2024

Department of Uvea, Sankara Nethralaya, Chennai, Tamil Nadu, India.

The white dot syndromes are a group of phenotypically similar disorders characterized by multiple lesions at the level of the outer retina, retinal pigment epithelium, and choroid. Common white dot syndromes whose imaging modalities have been described in this article are multiple evanescent white dot syndrome, acute posterior multifocal placoid pigment epitheliopathy, acute zonal occult outer retinopathy, multifocal choroiditis and panuveitis, punctate inner choroidopathy, serpiginous choroiditis, and birdshot chorioretinopathy. The various imaging modalities help us to better understand the pathophysiology of the various entities and help in diagnosing, monitoring, and prognosticating them.

View Article and Find Full Text PDF
Article Synopsis
  • Indocyanine green angiography (ICGA) is crucial for diagnosing and tracking choroidal inflammation, particularly choroidal vasculitis, which is often missed by doctors not using this method during posterior uveitis assessments.
  • The study analyzes ICGA signs of choroidal vasculitis, highlighting two main patterns: choriocapillaritis, which shows hypofluorescent areas indicating inflammation, and stromal choroidal vasculitis, characterized by leaking hyperfluorescent vessels.
  • Overall, choroidal vasculitis is commonly found in patients with inflammatory choroid issues, and understanding its ICGA features can improve diagnosis and treatment outcomes.
View Article and Find Full Text PDF

Purpose: To describe the multimodal imaging findings of a rare case of multiple evanescent white dot syndrome (MEWDS) associated with COVID-19.

Methods: A case report was analyzed and described alongside COVID-19 associated MEWDS cases identified in the current literature.

Results: A healthy 20-year-old man was evaluated after a three-day history of blurry vision occurring two months after COVID-19 infection.

View Article and Find Full Text PDF
Article Synopsis
  • A 16-year-old female experienced blurred vision in her left eye and was diagnosed with possible multiple evanescent white dot syndrome (MEWDS) secondary to acute retinal pigment epitheliitis (ARPE) after evaluation at the ophthalmology department.
  • Initial tests showed significant differences in visual acuity between her eyes, with abnormalities in retinal structure identified through imaging techniques like optical coherence tomography (OCT) and fundus autofluorescence (FAF).
  • After a two-week period with no treatment, her visual acuity improved and retinal abnormalities resolved, but there was an increase in white spots observed, indicating the complex nature of the two conditions—ARPE and MEWDS—making them potentially difficult to differentiate.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!