Abstract |
In a retrospective, clinico-histological study, 84 corneas from 73 patients with diagnosed Fuchs' dystrophy (FD) were examined after penetrating keratoplasty. Seven types of posterior corneal degeneration were found: six with diversely arranged and pronounced guttae and a thickened Descemet's membrane, and a seventh with no guttae in either eye. This last variant appeared histologically in only two patients. Whether it represents a different syndrome can only be speculated. Our study showed, however, that the frequency of cornea guttata (CG) in FD is statistically significant in all the histological variants.
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Authors | W Lisch, M Buob, K P Steuhl |
Journal | Klinische Monatsblatter fur Augenheilkunde
(Klin Monbl Augenheilkd)
Vol. 198
Issue 2
Pg. 83-6
(Feb 1991)
ISSN: 0023-2165 [Print] Germany |
Vernacular Title | Cornea guttata und Fuchssche Hornhaut-Endothel-Epithel-Dystrophie. Klinisch-histologische Studie bei 73 Patienten. |
PMID | 2041372
(Publication Type: English Abstract, Journal Article)
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Topics |
- Aged
- Aged, 80 and over
- Cornea
(pathology)
- Corneal Edema
(pathology)
- Corneal Opacity
(pathology)
- Descemet Membrane
(pathology)
- Female
- Fuchs' Endothelial Dystrophy
(pathology, surgery)
- Humans
- Keratoplasty, Penetrating
- Male
- Microscopy
- Retrospective Studies
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