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Terrien marginal degeneration.
Ding, Yanning; Murri, Michael S; Birdsong, Orry C; Ronquillo, Yasmyne; Moshirfar, Majid.
Afiliação
  • Ding Y; HDR Research Center, Hoopes Vision, Draper, UT, United States.
  • Murri MS; John A. Moran Eye Center, Department of Ophthalmology and Visual Sciences, University of Utah School of Medicine, Salt Lake City, UT, United States.
  • Birdsong OC; HDR Research Center, Hoopes Vision, Draper, UT, United States.
  • Ronquillo Y; HDR Research Center, Hoopes Vision, Draper, UT, United States; Department of Biology, University of Utah, Salt Lake City, Utah, United States.
  • Moshirfar M; HDR Research Center, Hoopes Vision, Draper, UT, United States; John A. Moran Eye Center, Department of Ophthalmology and Visual Sciences, University of Utah School of Medicine, Salt Lake City, UT, United States; Department of Biology, University of Utah, Salt Lake City, Utah, United States; Utah Lio
Surv Ophthalmol ; 64(2): 162-174, 2019.
Article em En | MEDLINE | ID: mdl-30316804
ABSTRACT
Terrien marginal degeneration, a rare disease resulting in peripheral corneal thinning, commonly occurs in middle-aged males and usually manifests clinically with decreased visual acuity from increased corneal astigmatism. Although the exact etiology is unknown, hypotheses focus on possible degenerative and inflammatory origins. Histopathologic studies often reveal characteristic findings of innumerable intracellular and extracellular vacuoles in the affected stroma. Distinguishing Terrien marginal degeneration from other peripheral corneal diseases such as Mooren ulcer and pellucid marginal degeneration is important. Nonsurgical interventions include spectacles, rigid gas-permeable contact lenses, and scleral lenses; however, when the corneal thickness is ≤150 µm, surgical interventions including tectonic grafting and lamellar keratoplasty may be necessary.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofias Hereditárias da Córnea / Doenças Raras Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofias Hereditárias da Córnea / Doenças Raras Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article