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Middle East Afr J Ophthalmol ; 29(3): 159-162, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-37408726

RESUMO

Anterior scleritis is rarely diagnosed with a peripheral amelanotic subretinal mass. We reported a rare case of a 31-year-old woman who was referred for suspected left eye choroidal melanoma. The patient had granulomatosis with polyangiitis with a history of treated left eye necrotizing anterior scleritis. Her left eye examination revealed 20/60 vision, superotemporal diffuse scleral injection, and thinning. Dilated fundus examination of the left eye showed a large peripheral amelanotic subretinal mass below the area of anterior scleritis, optic disc hyperemia, and subretinal fluid. The patient was successfully treated with intravenous methylprednisolone, rituximab infusions, and oral methotrexate. Two months after treatment, her vision improved to 20/20, with inactive anterior scleritis and a significant reduction in the subretinal mass with complete resolution of optic disc hyperemia and subretinal fluid. High index of suspicion of this atypical presentation of anterior scleritis is important to avoid aggressive modalities of treatment.


Assuntos
Granulomatose com Poliangiite , Hiperemia , Esclerite , Feminino , Humanos , Adulto , Granulomatose com Poliangiite/complicações , Granulomatose com Poliangiite/diagnóstico , Esclerite/diagnóstico , Esclerite/tratamento farmacológico , Esclerite/etiologia , Hiperemia/complicações , Metilprednisolona , Glucocorticoides/uso terapêutico
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