Serpiginous choroiditis represents an inflammation, often asymmetric, situated at the level of the inner choroid, which is related to the retinal pigment epithelium and the choriocapillaris. It is known as a primarily idiopathic, but there are authors who consider it an autoimmune process. Many times, fundus autofluorescence is the investigation which is guiding the diagnosis, the management, also the follow-up together with the determination of the progressive visual prognosis. Local treatment is proven to be sometimes an adjunctive treatment often effective. SC = Serpiginous choroiditis; RPE = Retinal pigment epithelium.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256075PMC

Publication Analysis

Top Keywords

serpiginous choroiditis
12
retinal pigment
8
pigment epithelium
8
macular serpiginous
4
choroiditis case
4
case report
4
report serpiginous
4
choroiditis represents
4
represents inflammation
4
inflammation asymmetric
4

Similar Publications

Purpose: To describe the clinical and imaging characteristics of the acute progressive phase of a recently proposed clinical entity, Multizonal Outer Retinopathy and Retinal Pigment Epitheliopathy (MORR), a variant of Acute Zonal Occult Outer Retinopathy (AZOOR).

Methods: Single observational case report.

Results: We present the case of a 49-year-old myopic female with progressive outer retinopathy most consistent with a diagnosis of MORR.

View Article and Find Full Text PDF

Purpose: To report a complex case of serpiginous-like choroiditis (SLC) in a patient with anti-neutrophil cytoplasmic antibody (ANCA)-anti-proteinase 3 (PR3)-associated vasculitis with systemic involvement.

Methods: Case report.

Results: A 40-year-old male from a tuberculosis (TB)-endemic region presented with bilateral active SLC lesions.

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

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!