Literature DB >> 15013878

The white dot syndromes.

David A Quillen1, Janet B Davis, Justin L Gottlieb, Barbara A Blodi, David G Callanan, Tom S Chang, Robert A Equi.   

Abstract

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

Entities:  

Mesh:

Year:  2004        PMID: 15013878     DOI: 10.1016/j.ajo.2004.01.053

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  35 in total

1.  Photoreceptor atrophy in acute posterior multifocal placoid pigment epitheliopathy demonstrated by optical coherence tomography.

Authors:  Tina A Scheufele; Andre J Witkin; Lisa S Schocket; Adam H Rogers; Joel S Schuman; Tony H Ko; James G Fujimoto; Elias Reichel; Jay S Duker
Journal:  Retina       Date:  2005-12       Impact factor: 4.256

2.  Fundus autofluorescence in serpiginous choroiditis.

Authors:  Felice Cardillo Piccolino; Andrea Grosso; Elisa Savini
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2008-09-19       Impact factor: 3.117

Review 3.  The use of SD-OCT in the differential diagnosis of dots, spots and other white retinal lesions.

Authors:  Elena Zaharova; Jerome Sherman
Journal:  Eye Brain       Date:  2011-10-25

4.  Vascular rarefaction at the choriocapillaris in acute posterior multifocal placoid pigment epitheliopathy viewed on OCT angiography.

Authors:  Reiko Kinouchi; Noriko Nishikawa; Akihiro Ishibazawa; Akitoshi Yoshida
Journal:  Int Ophthalmol       Date:  2016-07-28       Impact factor: 2.031

5.  [White dot syndromes : Principles, diagnostics, and treatment].

Authors:  Dominika Pohlmann; Sibylle Winterhalter; Uwe Pleyer
Journal:  Ophthalmologe       Date:  2019-12       Impact factor: 1.059

6.  White dot syndromes: a 20-year study of incidence, clinical features, and outcomes.

Authors:  Nakhleh E Abu-Yaghi; Stella P Hartono; David O Hodge; Jose S Pulido; Sophie J Bakri
Journal:  Ocul Immunol Inflamm       Date:  2011-12       Impact factor: 3.070

7.  Cone photoreceptor abnormalities correlate with vision loss in a case of acute posterior multifocal placoid pigment epitheliopathy.

Authors:  In Hwan Hong; Sung Pyo Park; Ching Lung Chen; Hyoung Kyun Kim; Stephen H Tsang; Stanley Chang
Journal:  Ophthalmic Surg Lasers Imaging Retina       Date:  2014 Jan-Feb       Impact factor: 1.300

8.  Temporally independent association of multiple evanescent white dot syndrome and optic neuritis.

Authors:  Christopher D Conrady; Therese Sassalos; Wayne T Cornblath; David N Zacks; Mark W Johnson
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2021-05-29       Impact factor: 3.117

Review 9.  Retinal Diseases that Can Masquerade as Neurological Causes of Vision Loss.

Authors:  Tanyatuth Padungkiatsagul; Loh-Shan Leung; Heather E Moss
Journal:  Curr Neurol Neurosci Rep       Date:  2020-09-15       Impact factor: 5.081

Review 10.  [White dot syndrome].

Authors:  W Göbel
Journal:  Ophthalmologe       Date:  2008-01       Impact factor: 1.059

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