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Vogt-Koyanagi-Harada disease: the step-by-step approach to a better understanding of clinicopathology, immunopathology, diagnosis, and management: a brief review.
Urzua, Cristhian A; Herbort, Carl P; Takeuchi, Masaru; Schlaen, Ariel; Concha-Del-Rio, Luz E; Usui, Yoshihiko; Cuitino, Loreto; Papasavvas, Ioannis.
Afiliação
  • Urzua CA; Laboratory of Ocular and Systemic Autoimmune Diseases, Faculty of Medicine, University of Chile, Santiago, Chile. cristhian.urzua@uchile.cl.
  • Herbort CP; Department of Ophthalmology, University of Chile, Santiago, Chile. cristhian.urzua@uchile.cl.
  • Takeuchi M; Facultad de Medicina, Clinica Alemana-Universidad del Desarrollo, Santiago, Chile. cristhian.urzua@uchile.cl.
  • Schlaen A; Retinal and Inflammatory Eye Diseases, Centre for Ophthalmic Specialised Care (COS), Lausanne, Switzerland.
  • Concha-Del-Rio LE; Department of Ophthalmology, National Defense Medical College, Tokorozawa, Saitama, Japan.
  • Usui Y; Hospital Universitario Austral, Hospital de Clinicas de Buenos Aires, Buenos Aires, Argentina.
  • Cuitino L; Inflammatory Eye Disease Clinic, Dr. Luis Sanchez Bulnes Hospital, Asociación para Evitar la Ceguera en México (APEC), Mexico City, CDMX, Mexico.
  • Papasavvas I; Department of Ophthalmology, Tokyo Medical University, Tokyo, Japan.
J Ophthalmic Inflamm Infect ; 12(1): 17, 2022 May 12.
Article em En | MEDLINE | ID: mdl-35553272
BACKGROUND: 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Screening_studies Idioma: En Revista: J Ophthalmic Inflamm Infect Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Chile País de publicação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Screening_studies Idioma: En Revista: J Ophthalmic Inflamm Infect Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Chile País de publicação: Alemanha