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C3 glomerulopathy associated with both hypertensive retinopathy and purtscher-like retinopathy.
Zaidi, Moosa; Mishra, Kapil; Nguyen, Huy Vu; Miller, Paul Peter; Ghoraba, Hashem; Karaca, Irmak; Matsumiya, Wataru; Nguyen, Quan Dong; Leung, Loh-Shan Bryan.
  • Zaidi M; Department of Ophthalmology, Byers Eye Institute, Stanford University School of Medicine, 2452 Watson Court, Palo Alto, CA, 94303, USA.
  • Mishra K; Department of Ophthalmology, Byers Eye Institute, Stanford University School of Medicine, 2452 Watson Court, Palo Alto, CA, 94303, USA.
  • Nguyen HV; Department of Ophthalmology, Byers Eye Institute, Stanford University School of Medicine, 2452 Watson Court, Palo Alto, CA, 94303, USA.
  • Miller PP; Department of Pathology, Stanford University School of Medicine, Lane Building, L235, 300 Pasteur Drive, Stanford, CA, 94305, USA.
  • Ghoraba H; Department of Ophthalmology, Byers Eye Institute, Stanford University School of Medicine, 2452 Watson Court, Palo Alto, CA, 94303, USA.
  • Karaca I; Department of Ophthalmology, Byers Eye Institute, Stanford University School of Medicine, 2452 Watson Court, Palo Alto, CA, 94303, USA.
  • Matsumiya W; Department of Ophthalmology, Byers Eye Institute, Stanford University School of Medicine, 2452 Watson Court, Palo Alto, CA, 94303, USA.
  • Nguyen QD; Department of Ophthalmology, Byers Eye Institute, Stanford University School of Medicine, 2452 Watson Court, Palo Alto, CA, 94303, USA.
  • Leung LB; Department of Ophthalmology, Byers Eye Institute, Stanford University School of Medicine, 2452 Watson Court, Palo Alto, CA, 94303, USA.
Am J Ophthalmol Case Rep ; 27: 101683, 2022 Sep.
Article in English | MEDLINE | ID: covidwho-1995948
ABSTRACT

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.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Case report / Cohort study / Observational study / Prognostic study Language: English Journal: Am J Ophthalmol Case Rep Year: 2022 Document Type: Article Affiliation country: J.ajoc.2022.101683

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Case report / Cohort study / Observational study / Prognostic study Language: English Journal: Am J Ophthalmol Case Rep Year: 2022 Document Type: Article Affiliation country: J.ajoc.2022.101683