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Bilateral Granulomatous Iridocyclitis Associated with Early-Onset Juvenile Psoriatic Arthritis

PURPOSE: The purpose of this study is to report on a case of bilateral granulomatous iridocyclitis in a patient with early-onset juvenile psoriatic arthritis (JPsA). METHODS: The method used is an observational case report. Observations. A 3-year-old Hispanic girl was sent to our uveitis service for...

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Detalles Bibliográficos
Autores principales: Nieves-Ríos, Christian, Requejo Figueroa, Guillermo A., Ayala Rodríguez, Sofía C., Santiago-Díaz, Alejandra, Rodriguez-Garcia, Eduardo J., Perez, Alejandro L., Rivera-Grana, Erick, Figueroa-Díaz, Adriana C., Martín-García, Rafael, Oliver, Armando L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9568322/
https://www.ncbi.nlm.nih.gov/pubmed/36249177
http://dx.doi.org/10.1155/2022/3990406
Descripción
Sumario:PURPOSE: The purpose of this study is to report on a case of bilateral granulomatous iridocyclitis in a patient with early-onset juvenile psoriatic arthritis (JPsA). METHODS: The method used is an observational case report. Observations. A 3-year-old Hispanic girl was sent to our uveitis service for further evaluation of her granulomatous uveitis. The initial ophthalmologic examination revealed bilateral band keratopathy, large mutton-fat keratic precipitates, multiple posterior synechiae, and 4+ anterior chamber cells. The physical exam was notable for left knee edema and right axillary rash. Laboratory testing was remarkable for an erythrocyte sedimentation rate of 80 mm/h, positive antinuclear antibodies (1 : 1, 280), and negative human leukocyte antigen B27. A cutaneous biopsy was obtained, which confirmed the diagnosis of a psoriatic rash. Treatment with oral prednisolone and topical prednisolone acetate with atropine sulfate resulted in the complete resolution of the uveitis. Conclusion and Importance. Bilateral granulomatous iridocyclitis may be a rare presentation of ocular involvement in patients with early-onset JPsA.