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Authordc.contributor.authorUrzúa Salinas, Cristhian Alejandro
Authordc.contributor.authorHerbort, Carl P.
Authordc.contributor.authorTakeuchi, Masaru
Authordc.contributor.authorSchlaen, Ariel
Authordc.contributor.authorConcha del Río, Luz E.
Authordc.contributor.authorUsui, Yoshihiko
Authordc.contributor.authorCuitino, Loreto
Authordc.contributor.authorPapasavvas, Ioannis
Admission datedc.date.accessioned2023-09-26T19:45:21Z
Available datedc.date.available2023-09-26T19:45:21Z
Publication datedc.date.issued2022
Cita de ítemdc.identifier.citationJournal of Ophthalmic Inflammation and Infection (2022) 12:17es_ES
Identifierdc.identifier.other10.1186/s12348-022-00293-3
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/195853
Abstractdc.description.abstractBackground Appraisals of Vogt-Koyanagi-Harada disease (VKH) have become progressively more complete, since its first description in 1906. The availability of new investigational methods has improved our knowledge of the immunopathology, clinicopathology, diagnosis, and management of VKH disease. This review aimed to describe some of the steps that led to better characterization of VKH as a clinical entity. Methods We searched on PubMed for articles that described the history of VKH disease and analyzed the progress in disease appraisal with new investigational and imaging methods. In particular, we searched for articles that investigated the clinicopathology, diagnosis, and management of VKH. Findings The following developments were considered essential for improving the appraisal and understanding of VKH: (1) the history of the disease, (2) immunopathological mechanisms, (3) clinicopathology, (4) the importance of distinguishing initial-onset from chronic disease, (5) relevant imaging modalities, among which indocyanine green angiography is crucial, (6) diagnostic criteria that facilitate early diagnosis, and (7) the need for early, prolonged, aggressive treatment that combines steroidal and non-steroidal immunosuppression. Conclusion Based on these findings, the definition of VKH has improved. VKH disease starts in the choroidal stroma and later involves other structures when it is not diagnosed and treated early. Indocyanine green angiography and enhanced depth imaging optical coherence tomography facilitate early diagnosis and precise monitoring of choroidal inflammation. ICGA is clearly the gold standard for appraisals and follow-ups in VKH disease, however EDI-OCT should be especially considered in those areas where ICGA is not fully available. These modalities have contributed substantially to a "cure" for VKH, when treatment is introduced within the therapeutic window of opportunity.es_ES
Patrocinadordc.description.sponsorshipNational Agency for Research and Development (ANID) grant Fondecyt Regular 1212038 Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) CONICYT FONDECYT 11191215es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherSpringeres_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
Sourcedc.sourceJournal of Ophthalmic Inflammation and Infectiones_ES
Keywordsdc.subjectChronic VKHes_ES
Keywordsdc.subjectInitial-onset acute VKHes_ES
Keywordsdc.subjectVogt-Koyanagi-Harada diseasees_ES
Keywordsdc.subjectUveomeningoencephalitic syndromees_ES
Títulodc.titleVogt-Koyanagi-Harada disease: the stepby- step approach to a better understanding of clinicopathology, immunopathology, diagnosis, and management: a brief reviewes_ES
Document typedc.typeArtículo de revistaes_ES
dc.description.versiondc.description.versionVersión publicada - versión final del editores_ES
dcterms.accessRightsdcterms.accessRightsAcceso abiertoes_ES
Catalogueruchile.catalogadorapces_ES
Indexationuchile.indexArtículo de publícación WoSes_ES


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Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States