Flashcards on Retinal and Uveal Disorders in Ophthalmology

Retinal and Uveal Disorders in Ophthalmology Explained

1 / 69

What are White Dot Syndromes (WDS)?

A group of idiopathic inflammatory chorioretinopathies characterized by whitish‑yellow lesions in the choroid, RPE, choriocapillaris and/or sensory re

Tap to flip · Swipe to navigate

White dot syndromes overview

69 cards

Card 1

Question: What are White Dot Syndromes (WDS)?

Answer: A group of idiopathic inflammatory chorioretinopathies characterized by whitish‑yellow lesions in the choroid, RPE, choriocapillaris and/or sensory re

Card 2

Question: What tissues are primarily involved in WDS lesions?

Answer: Choroid, retinal pigment epithelium (RPE), choriocapillaris and/or sensory retina (and sometimes vitreous).

Card 3

Question: Are White Dot Syndromes considered infectious diseases?

Answer: As a group they are considered idiopathic inflammatory (not infectious); individual entities may be suspected of infectious triggers but no consistent

Card 4

Question: What underlying mechanism is presumed for WDS?

Answer: An autoimmune mechanism is presumed (immune reaction to choriocapillaris/RPE in predisposed individuals).

Card 5

Question: What common clinical finding unites the WDS group?

Answer: The presence of multiple yellow‑white lesions (white dots) at some point in the disease course—though not every entity always shows obvious 'white dot

Card 6

Question: How are WDS generally diagnosed?

Answer: Based on medical history, demographics, clinical exam and ancillary testing (FA, ICGA, FAF, OCT, electrodiagnostics, labs, clinical course).

Card 7

Question: What are general management options for WDS?

Answer: Observation, local or systemic steroids, immunomodulatory agents, laser photocoagulation or photodynamic therapy depending on the entity and complicat

Card 8

Question: Which WDS is typically unilateral?

Answer: Multiple Evanescent White Dot Syndrome (MEWDS) is typically unilateral.

Card 9

Question: Which WDS conditions are listed in this overview?

Answer: MEWDS, AZOOR, APMPPE, PIC, Multifocal choroiditis and panuveitis (MCP), ARPE (acute retinal pigment epitheliitis/Krill's disease), Birdshot retinochor

Card 10

Question: Which WDS are more common in younger patients and which in older?

Answer: Most WDS affect younger patients; exceptions include Birdshot retinochoroidopathy and Serpiginous choroiditis which occur in older individuals.