Medical

White Dot Syndrome

Any of a group of idiopathic multifocal inflammatory conditions involving the retina and the choroid characterised by the appearance of white dots in the fundus, which typically affect young, healthy, myopic women
Examples Multiple evanescent white dot syndrome (MEWDS), multifocal choroiditis & panuveitis (MCP), punctate inner choroidopathy (PIC), acute posterior multifocal placoid pigment epitheliopathy (APMPPE), serpiginous choroiditis, birdshot retinochoroidopathy
DiffDx Diffuse unilateral subacute neuroretinitis, punctate outer retinal toxoplasmosis, sarcoidosis, tuberculosis, syphilis, presumed ocular histoplasmosis, septic emboli, pars planitis, and sympathetic ophthalmia
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.
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References in periodicals archive
Several features of PCD could also be consistent with postinflammatory changes of a retinal white dot syndrome [19, 56-65].
Freund et al., "Fundus autofluorescence and photoreceptor bleaching in multiple evanescent white dot syndrome," Ophthalmic Surgery, Lasers and Imaging Retina, vol.
Multiple evanescent white dot syndrome (MEWDS) was first described in 1984 as a rare, sudden onset of unilateral chorioretinopathy, with the predominant sign being multifocal yellow-white spots throughout the retina [1, 2].
Gilbert, "Multiple evanescent white dot syndrome. I.
In PubMed, the term "multifocal evanescent white dot syndrome," using all or parts of the term, brought up 151 articles.
Multiple Evanescent White Dot Syndrome. Multiple evanescent white dot syndrome (MEWDS) is a retinochoroiditis that is typically described in young myopic females and is occasionally preceded by a viral prodrome.
The recent use of "en-face" enhanced-depth imaging spectral-domain optical coherence tomography (EDI SD-OCT) helps distinguish the retinal layers involved in the physiopathology of multiple evanescent white dot syndrome (MEWDS).
Miller, "Distinguishing white dot syndromes with patterns of choroidal hypoperfusion on optical coherence tomography angiography," Ophthalmic Surgery, Lasers and Imaging Retina, vol.
Though rare, lyme disease should be considered in the differential diagnosis of white dot syndromes (see pages 241-243).
Practical knowledge and current developments are delivered in an engaging question-and-answer format through 21 chapters covering the basic mechanisms of ocular inflammation; signs, symptoms, and classification of uveitis; laboratory testing techniques; local and systemic treatments for all forms of uveitis; complications of the disease; systemic disease associations of uveitic conditions; differential diagnosis of different presentations; pars planitis and intermediate uveitis; infectious and autoimmune forms of posterior uveitis; and a review of the white dot syndromes. For current ophthalmology residents and fellows in training, and current practitioners wishing to augment their scope and depth of knowledge in the diagnosis and treatment of uveitis.
Punctate inner choroidopathy (PIC) is a posterior uveitis belonging to the group of idiopathic white dot syndromes. It tends to present in young to middle aged women with myopia [1].
White dot syndromes have been associated with various diseases that are characterized by delayed hypersensitivity reaction such as sarcoidosis, tuberculosis, schistosomiasis and also Lyme disease.
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