Abstract
Acute exudative polymorphous vitelliform maculopathy is an extremely rare retinal disorder, that has been considered as a form of paraneoplasic retinopathy, found in patients with a underlying primary tumor. Symptoms of acute exudative polymorphous vitelliform maculopathy include preceding headache followed by acute onset of vision loss. The fundus of a patient with this condition typically demonstrates bilateral, subretinal white-yellow deposits in the macular region. The report of a rare disease which has a strong association with underlying neoplasia is extremely relevant whereas it helps better comprehend its genuine history, possible complicacy and prognosis.
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Neves, G. de F., & Bastos, A. L. C. de M. (2017). Acute exsudative polymorphous vitelliform maculopathy: Case report. Revista Brasileira de Oftalmologia, 76(2), 94–97. https://doi.org/10.5935/0034-7280.20170019
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