Adult foveomacular vitelliform dystrophy

Detalhes bibliográficos
Autor(a) principal: Balarin,Valdir
Data de Publicação: 2013
Outros Autores: Lira,Rodrigo Pessoa Cavalcanti, Berezowsky,Michel, Torigoe,Andrea Mara Simões
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista Brasileira de Oftalmologia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0034-72802013000300013
Resumo: Adult foveomacular vitelliform dystrophy is a rare pathology. Less than 1% of the reported cases display perifoveal capillary permeability. The three-year follow-up period of the case revealed a rare form, which had not yet been documented. The patient was a 40-year-old female with normal visual acuity, and a minor complaint of metamorphopsia on the left eye. Retinography showed a perifoveal yellowish subretinal area OS.Angiography showed perifoveal leakage OS. Follow up showed that, over 3 years, capillary incompetence disappeared and the yellow area underwent alterations, becoming atrophic OS. Angiography also showed hyperfluorescence (windows defect). Towards the end, it resembled the appearance of late stage of Best's Disease.
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spelling Adult foveomacular vitelliform dystrophyMaculaMacular degenerationMacular edemaTelangiectasisCase reportsAdult foveomacular vitelliform dystrophy is a rare pathology. Less than 1% of the reported cases display perifoveal capillary permeability. The three-year follow-up period of the case revealed a rare form, which had not yet been documented. The patient was a 40-year-old female with normal visual acuity, and a minor complaint of metamorphopsia on the left eye. Retinography showed a perifoveal yellowish subretinal area OS.Angiography showed perifoveal leakage OS. Follow up showed that, over 3 years, capillary incompetence disappeared and the yellow area underwent alterations, becoming atrophic OS. Angiography also showed hyperfluorescence (windows defect). Towards the end, it resembled the appearance of late stage of Best's Disease.Sociedade Brasileira de Oftalmologia2013-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0034-72802013000300013Revista Brasileira de Oftalmologia v.72 n.3 2013reponame:Revista Brasileira de Oftalmologia (Online)instname:Sociedade Brasileira de Oftalmologia (SBO)instacron:SBO10.1590/S0034-72802013000300013info:eu-repo/semantics/openAccessBalarin,ValdirLira,Rodrigo Pessoa CavalcantiBerezowsky,MichelTorigoe,Andrea Mara Simõeseng2013-10-31T00:00:00Zoai:scielo:S0034-72802013000300013Revistahttps://rbo.emnuvens.com.br/rbo/indexhttps://old.scielo.br/oai/scielo-oai.phpsob@sboportal.org.br||rbo@sboportal.org.br1982-85510034-7280opendoar:2013-10-31T00:00Revista Brasileira de Oftalmologia (Online) - Sociedade Brasileira de Oftalmologia (SBO)false
dc.title.none.fl_str_mv Adult foveomacular vitelliform dystrophy
title Adult foveomacular vitelliform dystrophy
spellingShingle Adult foveomacular vitelliform dystrophy
Balarin,Valdir
Macula
Macular degeneration
Macular edema
Telangiectasis
Case reports
title_short Adult foveomacular vitelliform dystrophy
title_full Adult foveomacular vitelliform dystrophy
title_fullStr Adult foveomacular vitelliform dystrophy
title_full_unstemmed Adult foveomacular vitelliform dystrophy
title_sort Adult foveomacular vitelliform dystrophy
author Balarin,Valdir
author_facet Balarin,Valdir
Lira,Rodrigo Pessoa Cavalcanti
Berezowsky,Michel
Torigoe,Andrea Mara Simões
author_role author
author2 Lira,Rodrigo Pessoa Cavalcanti
Berezowsky,Michel
Torigoe,Andrea Mara Simões
author2_role author
author
author
dc.contributor.author.fl_str_mv Balarin,Valdir
Lira,Rodrigo Pessoa Cavalcanti
Berezowsky,Michel
Torigoe,Andrea Mara Simões
dc.subject.por.fl_str_mv Macula
Macular degeneration
Macular edema
Telangiectasis
Case reports
topic Macula
Macular degeneration
Macular edema
Telangiectasis
Case reports
description Adult foveomacular vitelliform dystrophy is a rare pathology. Less than 1% of the reported cases display perifoveal capillary permeability. The three-year follow-up period of the case revealed a rare form, which had not yet been documented. The patient was a 40-year-old female with normal visual acuity, and a minor complaint of metamorphopsia on the left eye. Retinography showed a perifoveal yellowish subretinal area OS.Angiography showed perifoveal leakage OS. Follow up showed that, over 3 years, capillary incompetence disappeared and the yellow area underwent alterations, becoming atrophic OS. Angiography also showed hyperfluorescence (windows defect). Towards the end, it resembled the appearance of late stage of Best's Disease.
publishDate 2013
dc.date.none.fl_str_mv 2013-06-01
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0034-72802013000300013
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0034-72802013000300013
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Oftalmologia
publisher.none.fl_str_mv Sociedade Brasileira de Oftalmologia
dc.source.none.fl_str_mv Revista Brasileira de Oftalmologia v.72 n.3 2013
reponame:Revista Brasileira de Oftalmologia (Online)
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