Literature DB >> 3061350

Posterior polymorphous dystrophy--a histopathologic presentation.

K Matsumoto1, P A Weber, T A Makley.   

Abstract

The corneal button from a 34-year-old woman with posterior polymorphous dystrophy was studied by light and electron microscopy. Ultrastructural findings showed coexistence of epithelial-like cells and abnormal endothelial cells, and Descemet's membrane composed of a normal anterior banded layer, and an irregular posterior homogeneous and collagenous layer. We suggest that these abnormal endothelial cells are in the process of transforming into epithelial-like cells.

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Year:  1988        PMID: 3061350

Source DB:  PubMed          Journal:  Ann Ophthalmol        ISSN: 0003-4886


  3 in total

1.  Exclusion of COL8A1, the gene encoding the alpha2(VIII) chain of type VIII collagen, as a candidate for Fuchs endothelial dystrophy and posterior polymorphous corneal dystrophy.

Authors:  J E Urquhart; S Biswas; G C M Black; F L Munier; J Sutphin
Journal:  Br J Ophthalmol       Date:  2006-11       Impact factor: 4.638

2.  A clinicopathologic study of posterior polymorphous dystrophy:implications for pathogenetic mechanism of the associated glaucoma.

Authors:  A B Threlkeld; W R Green; H A Quigley; Z de la Cruz; W J Stark
Journal:  Trans Am Ophthalmol Soc       Date:  1994

3.  Recurrence of posterior polymorphous corneal dystrophy is caused by the overgrowth of the original diseased host endothelium.

Authors:  Stanislava Merjava; Eva Malinova; Petra Liskova; Martin Filipec; Zuzana Zemanova; Kyra Michalova; Katerina Jirsova
Journal:  Histochem Cell Biol       Date:  2011-06-22       Impact factor: 4.304

  3 in total

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