Central cloudy corneal dystrophy of Francois. A clinicopathologic study.
Arch Ophthalmol
; 115(8): 1058-62, 1997 Aug.
Article
en En
| MEDLINE
| ID: mdl-9258229
ABSTRACT
Central cloudy corneal dystrophy of Francois was first described in 1955 by J. Francois; its pathophysiology remains unknown. An 80-year-old woman with bilateral central cloudy corneal dystrophy of Francois was examined after having undergone a combined penetrating keratoplasty and cataract extraction. The corneal button was obtained. Light microscopy revealed stromal staining for acid mucopolysaccharide. Transmission electron microscopy revealed extracellular vacuoles, some of which had fibrillogranular material and electron-dense deposits. Fibrillogranular material was present in and around some keratocytes. Numerous endothelial vacuoles contained light-staining fibrillogranular material and round electron-dense granules. Our findings suggest that the opacities in patients with central cloudy corneal dystrophy of Francois are due to the extracellular accumulation of mucopolysaccharide and lipidlike material. Further studies are needed to elucidate the nature of these deposits.
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Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Distrofias Hereditarias de la Córnea
/
Opacidad de la Córnea
Límite:
Aged
/
Aged80
/
Female
/
Humans
Idioma:
En
Revista:
Arch Ophthalmol
Año:
1997
Tipo del documento:
Article
País de afiliación:
Estados Unidos