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C3 glomerulopathy associated with both hypertensive retinopathy and purtscher-like retinopathy

PURPOSE: This article reports the case of a 21-year-old woman with both hypertensive retinopathy and Purtscher-like retinopathy in association with C3 glomerulopathy. OBSERVATIONS: The patient was referred for bilateral painless vision loss with posterior pole cotton wool spots, optic disc edema, an...

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Detalles Bibliográficos
Autores principales: Zaidi, Moosa, Mishra, Kapil, Nguyen, Huy Vu, Miller, Paul Peter, Ghoraba, Hashem, Karaca, Irmak, Matsumiya, Wataru, Nguyen, Quan Dong, Leung, Loh-Shan Bryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395975/
https://www.ncbi.nlm.nih.gov/pubmed/36016724
http://dx.doi.org/10.1016/j.ajoc.2022.101683
Descripción
Sumario:PURPOSE: This article reports the case of a 21-year-old woman with both hypertensive retinopathy and Purtscher-like retinopathy in association with C3 glomerulopathy. OBSERVATIONS: The patient was referred for bilateral painless vision loss with posterior pole cotton wool spots, optic disc edema, and confluent retinal whitening suggesting a mixed picture of hypertensive retinopathy, with initial blood pressure 236/152, and Purtscher-like retinopathy. She was subsequently diagnosed with C3 glomerulopathy which likely caused her severe hypertension and which likely occurred alongside Purtscher-like retinopathy due to a shared pathogenesis of complement dysregulation. Follow up examination and imaging revealed gradual improvement in visual acuity, almost complete resolution of fundus exam abnormalities, improvement in macular nonperfusion, resolution of disc leakage and choroidal leakage, resolution of macular edema, and residual outer retinal hyperreflective foci in both eyes. CONCLUSION AND IMPORTANCE: This case represents the first report of both Purtscher-like retinopathy and hypertensive retinopathy occurring in association with C3 glomerulopathy. It supports investigation of anti-complement therapy as a potential treatment for Purtscher-like retinopathy.