Coincident Pellucid Marginal Degeneration and Fuchsiridocyclitis: a case report
Ali Hendi Alghamdi

TL;DR
A rare case of two eye conditions, Pellucid Marginal Degeneration and Fuchs' uveitis, is reported, highlighting the challenges in diagnosis and treatment.
Contribution
This case report documents the rare coexistence of PMD and FHI, emphasizing the need for individualized surgical planning.
Findings
PMD and FHI coexistence is exceptionally rare and poses diagnostic and surgical challenges.
Multimodal imaging and tailored surgical strategies are essential for optimal outcomes.
Postoperative vigilance is crucial due to risks of glaucoma and persistent inflammation.
Abstract
We report a rare coexistence of Pellucid Marginal Degeneration (PMD) and Fuchs' heterochromic iridocyclitis (FHI) in a 40-year-old female. The overlap of corneal ectasia and chronic uveitis created significant diagnostic and surgical challenges, highlighting the importance of individualized planning in complex anterior segment diseases. The patient presented with painless, progressive visual decline in the right eye. Clinical examination revealed inferior corneal thinning, mature cataract, pigmented keratic precipitates, and peripheral anterior synechiae (PAS). Corneal tomography confirmed PMD with a characteristic “crab-claw” pattern. The patient underwent phacoemulsification with posterior chamber intraocular lens implantation. Postoperatively, visual acuity improved, although optic disc cupping and persistent PAS underscored the need for long-term glaucoma surveillance. The…
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Taxonomy
TopicsCorneal surgery and disorders · Glaucoma and retinal disorders · Immune Response and Inflammation
