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American Journal of Ophthalmology 2004-Mar

The white dot syndromes.

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
David A Quillen
Janet B Davis
Justin L Gottlieb
Barbara A Blodi
David G Callanan
Tom S Chang
Robert A Equi

Maneno muhimu

Kikemikali

OBJECTIVE

To review the distinctive and shared features of the white dot syndromes, highlighting the clinical findings, diagnostic test results, proposed etiologies, treatments, and prognosis.

METHODS

Review.

METHODS

Review of the literature.

RESULTS

Common white dot syndromes are reviewed, including acute posterior multifocal placoid pigment epitheliopathy, birdshot chorioretinopathy, diffuse unilateral subacute neuroretinitis, multiple evanescent white dot syndrome, multifocal choroiditis with panuveitis, serpiginous choroiditis, and acute zonal occult outer retinopathy.

CONCLUSIONS

The white dot syndromes are a group of disorders characterized by multiple whitish-yellow inflammatory lesions located at the level of the outer retina, retinal pigment epithelium, and choroid. For clinicians and researchers alike, they present significant diagnostic and therapeutic challenges.

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