Purtscher-like retinopathies (PLRs) are occlusive retinal microangiopathies arising from non-traumatic etiologies with characteristic fundus findings. We present a case of PLR secondary to typical hemolytic uremic syndrome (HUS) that achieved an excellent visual outcome with treatment of the systemic disease alone. This report highlights that PLR should be considered as a differential for retinopathy in the setting of systemic illness. Furthermore, the treatment of the precipitant cause should be prioritized, with ongoing monitoring of visual function and screening for chronic ischemic complications.
Cite this paper
Zhang, L. , Meyerov, J. , Dong, M. and Singh, N. (2024). Purtscher-Like Retinopathy in Hemolytic Uremic Syndrome: A Case Report. Open Access Library Journal, 11, e2445. doi: http://dx.doi.org/10.4236/oalib.1112445.
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