gms | German Medical Science

102. Jahrestagung der DOG

Deutsche Ophthalmologische Gesellschaft e. V.

23. bis 26.09.2004, Berlin

Alterations in the structure of the epiretinal membranes in PVR: assumptions and reality

Meeting Abstract

  • corresponding author C. Vidinova - Clinic of Ophthalmology, Military Medical Academy, Sofia, Bulgaria
  • L. Voinov - Clinic of Ophthalmology, Military Medical Academy, Sofia, Bulgaria
  • N. Vidinov - Department of Anatomy, Medical University, Sofia, Bulgaria
  • P. Gougoutchkova - Department of Ophthalmology, Medical University, Sofia, Bulgaria

Evidenzbasierte Medizin - Anspruch und Wirklichkeit. 102. Jahrestagung der Deutschen Ophthalmologischen Gesellschaft. Berlin, 23.-26.09.2004. Düsseldorf, Köln: German Medical Science; 2004. Doc04dogDO.03.07

Die elektronische Version dieses Artikels ist vollständig und ist verfügbar unter: http://www.egms.de/de/meetings/dog2004/04dog024.shtml

Veröffentlicht: 22. September 2004

© 2004 Vidinova et al.
Dieser Artikel ist ein Open Access-Artikel und steht unter den Creative Commons Lizenzbedingungen (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.de). Er darf vervielfältigt, verbreitet und öffentlich zugänglich gemacht werden, vorausgesetzt dass Autor und Quelle genannt werden.


Gliederung

Text

Objective

Proliferative Vitreoretinopathy (PVR) is known to be the main cause for failure of the routine retinal detachment surgery. Our aim was to follow and document the changes in the ultrastructure of the epiretinal membranes in different stages of PVR.

Methods

Epiretinal membranes were taken during vitrectomy of 34 patients with different stages of PVR and further analysed with transmission and scanning electron microscopy, according to routine techniques. Patients were precisely ophtalmologically examined prior to operation and an OCT image of the fundus was made in all cases.

Results

In the relatively early stages of the disease (B-C1 stages) mainly retinal pigment epithelial (RPE) cells, fibroblasts and occasional glial cells were found. Moreover some of the RPE cells showed altered characteristics- limited number of pigment granules, changes in shape, clustering of mitochondrial complexes around the cell nucleus. In the extracellular matrix single collagen fibres -type II were observed. In contrast, the epiretinal membranes from the developed stages of PVR were comprised mostly of fibroblasts and considerably diminished number of RPE cells. Cells with marks of degenerations were generally found. Rough collagen bundles type I were seen in the matrix and the number of proteoglycan complexes was significantly enlarged.

Conclusions

Our results point out that epiretinal membranes in PVR are dynamic structures, constantly changing their cell and matrix composition with the progression of the disease. The morphological changes together with the clinical (OCT) data are important to consider when discussing the most appropriate therapeutical approach for each case.