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An ultrastructural investigation of an early manifestation of the posterior polymorphous dystrophy of the cornea.

Publication ,  Journal Article
Sekundo, W; Lee, WR; Kirkness, CM; Aitken, DA; Fleck, B
Published in: Ophthalmology
August 1994

BACKGROUND: Posterior polymorphous dystrophy of the cornea is an uncommon, but well-recognized, congenital disease affecting Descemet's membrane and endothelium. Visual impairment usually is minimal and slowly progressive. Edema develops in a small number of patients, necessitating a corneal graft in middle age. An early manifestation of posterior polymorphous dystrophy with corneal edema present at birth or soon thereafter is extremely rare; only a few ultrastructural reports are available. METHODS: The corneal button of a 5-month-old baby with posterior polymorphous dystrophy was examined by conventional light and electron microscopy. FINDINGS: The anterior banded zone of Descemet's membrane was thinned (2 microns) in the axial part of the cornea, contained defects in the paraxial part, and was absent at the periphery. Where present, the anterior banded zone was lined posteriorly by a fibrocellular layer (containing fibroblast-like spindle cells and striated collagen fibrils) and a fibrillar layer forming an abnormal posterior collagenous layer. This layer was lined posteriorly by degenerate overlapping endothelial cells, which also were in apposition to the stroma in regions with an absent anterior banded zone. The defects in Descemet's membrane were used by the abnormal keratocytes to migrate between the anterior banded zone and the posterior collagenous layer. At the periphery, a multilayer of spindle cells was present behind the stroma. CONCLUSIONS: Failure to produce a continuous anterior banded zone indicates an onset of the disease before the twelfth week of gestation. It appears that, in posterior polymorphous dystrophy, there is a mosaic of better preserved and dystrophic endothelial cells and that the presence or absence of the normal components of Descemet's membrane is determined by the proportion of dystrophic cells in the endothelial cell population.

Duke Scholars

Published In

Ophthalmology

DOI

ISSN

0161-6420

Publication Date

August 1994

Volume

101

Issue

8

Start / End Page

1422 / 1431

Location

United States

Related Subject Headings

  • Pedigree
  • Ophthalmology & Optometry
  • Male
  • Keratoplasty, Penetrating
  • Infant
  • Humans
  • Endothelium, Corneal
  • Descemet Membrane
  • Corneal Dystrophies, Hereditary
  • Consanguinity
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Sekundo, W., Lee, W. R., Kirkness, C. M., Aitken, D. A., & Fleck, B. (1994). An ultrastructural investigation of an early manifestation of the posterior polymorphous dystrophy of the cornea. Ophthalmology, 101(8), 1422–1431. https://doi.org/10.1016/s0161-6420(94)31155-9
Sekundo, W., W. R. Lee, C. M. Kirkness, D. A. Aitken, and B. Fleck. “An ultrastructural investigation of an early manifestation of the posterior polymorphous dystrophy of the cornea.Ophthalmology 101, no. 8 (August 1994): 1422–31. https://doi.org/10.1016/s0161-6420(94)31155-9.
Sekundo W, Lee WR, Kirkness CM, Aitken DA, Fleck B. An ultrastructural investigation of an early manifestation of the posterior polymorphous dystrophy of the cornea. Ophthalmology. 1994 Aug;101(8):1422–31.
Sekundo, W., et al. “An ultrastructural investigation of an early manifestation of the posterior polymorphous dystrophy of the cornea.Ophthalmology, vol. 101, no. 8, Aug. 1994, pp. 1422–31. Pubmed, doi:10.1016/s0161-6420(94)31155-9.
Sekundo W, Lee WR, Kirkness CM, Aitken DA, Fleck B. An ultrastructural investigation of an early manifestation of the posterior polymorphous dystrophy of the cornea. Ophthalmology. 1994 Aug;101(8):1422–1431.
Journal cover image

Published In

Ophthalmology

DOI

ISSN

0161-6420

Publication Date

August 1994

Volume

101

Issue

8

Start / End Page

1422 / 1431

Location

United States

Related Subject Headings

  • Pedigree
  • Ophthalmology & Optometry
  • Male
  • Keratoplasty, Penetrating
  • Infant
  • Humans
  • Endothelium, Corneal
  • Descemet Membrane
  • Corneal Dystrophies, Hereditary
  • Consanguinity