Retinal arterial occlusive vasculitis following IgA nephropathy: A case report.
Vazquez-Membrillo MiguelRamírez-Solís FelipeZepeda-Palacio ClaudiaShrivastava AnuragLin KiraMarlon Rafael Garcia-RoaRomero-Morales VeronicaVillalpando-Gomez YolandaCorredor-Casas SoniaPublished in: European journal of ophthalmology (2022)
Although it is among the most commonly occurring forms of glomerulonephritis leading to renal failure, IgA nephropathy rarely presents with a bilateral retinal vasculopathy. Schölein - Henoch purpura, the other primary disease associated with glomerular IgA deposition, may be indistinguishable from primary IgA nephropathy. A comprehensive retinal examination with multimodal functional and structural ophthalmic diagnostic testing in conjunction with renal biopsy was needed to confirm the diagnosis. It is critical to include primary renal pathology when formulating a differential diagnosis for cases of bilateral retinal vasculitis, particularly in young otherwise healthy patients.