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Published on: August 6, 2021
Vancomycin-Associated Hemorrhagic Occlusive Retinal Vasculitis: A Clinical-Pathophysiological Analysis
Bozho Todorich1, Lisa J Faia1, Aristomenis Thanos1
1Associated Retinal Consultants, PC, Royal Oak, Michigan; Department of Ophthalmology, Oakland University William Beaumont School of Medicine, Rochester, Michigan.
Vancomycin-related hemorrhagic occlusive retinal vasculopathy (HORV) causes severe vision loss. Histopathology reveals necrotizing retinal vasculopathy and choroiditis, not vasculitis, suggesting a complex pathophysiology.
Area of Science:
- Ophthalmology
- Pathology
- Retinal Diseases
Background:
- Vancomycin-related hemorrhagic occlusive retinal vasculopathy (HORV) is a rare but severe condition.
- Understanding its pathophysiology is crucial for diagnosis and management.
Observation:
- Two patients with HORV post-cataract surgery presented with vision loss and pain.
- Clinicopathologic correlation included multimodal imaging, UBM, and histology.
- Histology showed iris/ciliary body infarction, hemorrhagic retinal necrosis, and occlusive choroidal vasculopathy.
Findings:
- HORV involves necrotizing retinal vasculopathy without retinal vasculitis.
- Chronic nongranulomatous choroiditis with T-cell infiltration was observed.
- A unique glomeruloid endothelial cell proliferation was noted in the choroid.
Implications:
- HORV pathophysiology is complex, differing from leukocytoclastic retinal vasculitis.
- Ocular pain may indicate severe ciliary body ischemia in HORV.
- These findings refine understanding of this vision-threatening condition.
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