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Sarcoidosis-related Uveitis: Clinical Presentation, Disease Course, and Rates of Systemic Disease Progression After Uveitis Diagnosis.
Ma, Shirley P; Rogers, Sophie L; Hall, Anthony J; Hodgson, Lauren; Brennan, Jessica; Stawell, Richard J; Lim, Lyndell L.
Afiliação
  • Ma SP; Centre for Eye Research Australia, East Melbourne, Victoria, Australia; Department of Ophthalmology, Alfred Health, Prahran, Victoria, Australia; Ocular Immunology Clinic, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
  • Rogers SL; Centre for Eye Research Australia, East Melbourne, Victoria, Australia.
  • Hall AJ; Eye Surgery Associates, East Melbourne, Victoria, Australia; Department of Ophthalmology, Alfred Health, Prahran, Victoria, Australia.
  • Hodgson L; Centre for Eye Research Australia, East Melbourne, Victoria, Australia.
  • Brennan J; Centre for Eye Research Australia, East Melbourne, Victoria, Australia.
  • Stawell RJ; Eye Surgery Associates, East Melbourne, Victoria, Australia; Ocular Immunology Clinic, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
  • Lim LL; Centre for Eye Research Australia, East Melbourne, Victoria, Australia; Eye Surgery Associates, East Melbourne, Victoria, Australia; Ocular Immunology Clinic, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia. Electronic address: limllp@unimelb.edu.au.
Am J Ophthalmol ; 198: 30-36, 2019 02.
Article em En | MEDLINE | ID: mdl-30243930
OBJECTIVE: To document the clinical presentation, treatment, and visual outcome of sarcoid uveitis and to determine the timing and potential risk factors of sarcoidosis progression to symptomatic systemic disease from the time of sarcoid uveitis diagnosis. DESIGN: Retrospective, interventional case series. METHODS: Subjects: Patients with dual diagnoses of uveitis and presumed/biopsy-proven sarcoidosis. PROCEDURE: Retrospective review of 143 patient records from the Royal Victorian Eye and Ear Hospital and Eye Surgery Associates in Melbourne, Australia, between October 1990 and April 2014 coded with the dual diagnoses of uveitis and sarcoidosis. Only patients with uveitis and presumed or biopsy-proven sarcoidosis (N = 113) were included. MAIN OUTCOME MEASURES: Ascertainment of rate and time (months) to the development of symptomatic systemic sarcoidosis from uveitis onset; comparison of the patient demographics, characteristics of uveitis, treatment, and visual outcome between those who developed systemic sarcoidosis and those who remained systemically asymptomatic. RESULTS: Uveitis was the initial presenting complaint of sarcoidosis in 78.8% (n = 89). Twenty-three patients had concurrent undiagnosed systemic disease at presentation and 29 subsequently developed symptomatic sarcoidosis in an organ uninvolved at uveitis onset. The median time to the development of symptomatic systemic sarcoidosis was 12 months. No statistically significant association was ascertained between any particular uveitis characteristic and extraocular sarcoidosis progression. CONCLUSION: Uveitis was the initial presentation of sarcoidosis in the vast majority of our subjects. Concurrent undiagnosed systemic sarcoidosis was common at the time of uveitis onset. A high index of suspicion for subsequent systemic progression should also be maintained, especially within the first 5 years of the uveitis diagnosis.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoidose / Uveíte / Oftalmopatias Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Ophthalmol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoidose / Uveíte / Oftalmopatias Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Ophthalmol Ano de publicação: 2019 Tipo de documento: Article