2013
DOI: 10.1097/ico.0b013e3182a64833
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Peripheral Pigmented Placoid Corneal Endotheliopathy

Abstract: Four healthy patients were noted to have PPPCE lesions. Although their etiology remains unknown, PPPCE behavior, morphology, and inferior corneal location suggest an origin from iris stromal melanocytes or iris pigment epithelium.

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Cited by 2 publications
(2 citation statements)
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“…To our knowledge, there have been 5 patients described to have PPPCE in the literature. Chen et al describe 4 asymptomatic patients (mean age, 53 years) with well-circumscribed brown pigmented lesions with scalloped or fimbriated edges located in the peripheral inferior corneal endothelium, similar to this patient. All 4 patients had brown irides.…”
Section: Discussionsupporting
confidence: 53%
“…To our knowledge, there have been 5 patients described to have PPPCE in the literature. Chen et al describe 4 asymptomatic patients (mean age, 53 years) with well-circumscribed brown pigmented lesions with scalloped or fimbriated edges located in the peripheral inferior corneal endothelium, similar to this patient. All 4 patients had brown irides.…”
Section: Discussionsupporting
confidence: 53%
“…There are few noncorneal conditions like chronic anterior uveitis, uncontrolled glaucoma, complicated intraocular surgeries, and immune-mediated endotheliopathy, which can cause endothelial dysfunction. [ 12 13 14 15 16 17 18 ] Nonsyphilitic deep interstitial keratitis shown by Holt and Watson had nummular features with vascularization along with inflammatory signs in anterior chamber. [ 10 ] All the above conditions are often symptomatic and are caused by the anterior stromal involvement with vascularization unlike nonvascular posterior opacity or semilunar sign of anterior scleritis.…”
Section: Discussionmentioning
confidence: 99%