Background: Our purpose was to describe the different morphological features in adult onset foveomacular vitelliform dystrophy (AOFVD), using en face enhanced depth imaging (EDI) spectral-domain optical coherence tomography (SD-OCT).

Methods: Thirty eyes of 22 consecutive patients presenting with diagnosis of AOFVD were enrolled. Diagnosis of AOFVD was concluded based on fundus examination, autofluorescence imaging, fluorescein angiography and SD-OCT. En face OCT imaging was obtained with the Spectralis EDI SD-OCT; 97 inverted sections (nine averaged B-scans per image) were acquired.

Results: On en face OCT, vitelliform lesions appeared as regular concentric rings of different reflectivity. From the periphery to center of the ring, we observed: (1) the hypereflective ring representing the inner segment/ outer segment (IS/OS) junction, which was continuous in 23 out of 30 eyes, and (2) a well-detectable hyporeflective ring between the IS/OS junction and vitelliform material in 20 out of 30 eyes; the innermost composant of the lesion was hypereflective, and it corresponded to vitelliform material. In eight out of 30 eyes, a hyporeflective "croissant"-shaped lesion with inferior concavity in the upper part of the hyperreflective material was present. Hypereflective retinal pigment epithelium (RPE) elevations or bumps were detected in 25 out of 30 eyes. These areas of focal RPE thickening or bumps appeared to be intensely hypereflective on infrared reflectance imaging.

Conclusion: En face imaging of the retina helps visualizing the distribution of vitelliform material in AOFVD. The sedimentation of vitelliform lesions is characterized by a upper "croissant"-shaped hypoflectivity. The bumps/thickening of RPE appeared as hypereflective lesions on IR imaging.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00417-013-2493-2DOI Listing

Publication Analysis

Top Keywords

vitelliform material
12
face enhanced
8
enhanced depth
8
depth imaging
8
optical coherence
8
coherence tomography
8
features adult
8
adult onset
8
onset foveomacular
8
foveomacular vitelliform
8

Similar Publications

Potential New Phenotypic Presentation of Pentosan Polysulfate Sodium Maculopathy.

J Vitreoretin Dis

August 2024

Retinal Consultants of Orange County, Fullerton, CA, USA.

Article Synopsis
  • - The case study highlights a new phenotypic presentation of maculopathy potentially linked to pentosan polysulfate sodium in a 55-year-old woman with interstitial cystitis who experienced vision changes after 10 years of treatment.
  • - Examination revealed retinal pigment epithelial hyperplasia and neurosensory retinal detachments that could easily be mistaken for other common eye conditions like age-related macular degeneration.
  • - Early diagnosis is critical; stopping the offending medication can prevent serious, irreversible damage to the retina and preserve vision.
View Article and Find Full Text PDF
Article Synopsis
  • The study aimed to simplify the electro-oculography (EOG) method and integrate it into the full-field electroretinogram (ffERG) protocol for better screening of retinal issues.
  • A comparison was made between standard EOG and the new screening EOG protocol with 20 control subjects and 5 patients with Best vitelliform macular dystrophy (BVMD), revealing both methods had similar accuracy in detecting retinal pigment epithelium (RPE) dysfunction.
  • Results showed the screening protocol was not only effective but also easier and more comfortable for patients, making it a potential preliminary test for assessing RPE function.
View Article and Find Full Text PDF

Adult-onset foveomacular vitelliform dystrophy (AOFVD) is a rare condition affecting the macula that presents diagnostic and management challenges due to its varied manifestations and clinical overlap with other retinal disorders. As vitelliform lesions can occur in various conditions, such as Best disease and age-related macular degeneration, clinical presentation, multimodal imaging findings, and genetic testing can aid in accurate diagnosis. Although AOFVD typically affects both eyes, unilateral involvement can occur.

View Article and Find Full Text PDF

Multifocal Vitelliform Paravascular Retinopathy (MVPR): A New Disorder in the Vitelliform Spectrum.

Am J Ophthalmol

January 2025

From the Stein Eye Institute (W.S., D.S.), University of California, Los Angeles, California, USA; Greater Los Angeles VA Healthcare Center (D.S.), Los Angeles, California, USA. Electronic address:

Purpose: To describe a new retinal phenotype characterized by bilateral, multifocal, subretinal vitelliform lesions along the vascular arcades that we refer to as multifocal vitelliform paravascular retinopathy (MVPR).

Design: Observational case series.

Methods: Multimodal retinal imaging including color fundus photography, fundus autofluorescence and cross sectional and en-face optical coherence tomography was performed to evaluate and characterize the lesions of MVPR.

View Article and Find Full Text PDF

Sub retinal pigment epithelium hyporeflective spaces preceding large drusen collapse.

Retina

August 2024

Retinal Disorders and Ophthalmic Genetics Division, Stein Eye Institute, University of California Los Angeles, David Geffen School of Medicine at UCLA, Los Angeles, California, United States.

Purpose: To describe and study hyporeflective sub retinal pigment epithelium (RPE) spaces in large drusen and drusenoid pigment epithelial detachment prior to collapse.

Method: Retrospective longitudinal study which enrolled patients with large and very large drusen due to intermediate age-related macular degeneration (AMD). The following optical coherence tomography (OCT) parameters were assessed: Drusen size (maximum width and height), OCT biomarkers of RPE atrophy, presence of intraretinal and subretinal fluid (IRF, SRF), acquired vitelliform lesion and sub RPE regions of hyporeflectivity within the PED compartment.

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!