Abstract 99. Jahrestagung der DOG, 29. 9. - 2. 10. 01 im ICC, Berlin

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Impressum



Histopathologic evaluation of retrocorneal membranes in failed corneal grafts

Wenkel H., Calabrese S., Seitz B., Küchle M., Naumann G. O. H.

Department of Ophthalmology, University Erlangen-Nürnberg, Schwabachanlage 6, D-91054 Erlangen

Purpose: To elucidate the frequency and typical patterns of retrocorneal membranes in graft failure after penetrating keratoplasty.
Patients and methods: Out of all 2800 penetrating keratoplasties performed between 1988 and 1998 all corneal buttons surgically excised for graft failure after penetrating keratoplasty were re-evaluated histopathologically. Out of 407 performed re-keratoplasties 371 corneal buttons (from 308 patients) were available for examination with sufficient clinical data. There were 180 male and 128 female patients with an age range from 6 to 88 years (median 62 years). The examined corneal buttons had been surgically excised 2 weeks to 37 years after the preceding penetrating keratoplasty (mean 3.5 years).
Results: A fibrous retrocorneal membrane was observed in 45% of the grafts with a thickness ranging from 2µm to 520µm (median 20µm). In 38 corneas there was iris tissue attached to the cornea, 68% (26/38) of these corneas presented retrocorneal membranes. Reendothelialization of the retrocorneal membrane was seen in 75 (45%) of the specimens. In 32% of the corneal buttons (120/371) the graft-host junction was visible. 56% of these corneas showed a retrocorneal membrane that had direct contact to the junction area in 92%. The occurrence of a retrocorneal membrane was not correlated to the original corneal disease leading to penetrating keratoplasty. Retrocorneal membranes were seen in corneal buttons excised 3 months to 28 years after the preceding keratoplasty.
Conclusions: Retrocorneal fibrous membranes were frequently seen in failed corneal grafts (45%). They seem to arise from downgrowth of stromal keratocytes through the graft-host junction but may also be a product of altered (metaplastic) endothelial cells.




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