Aim-To investigate effects of photodynamic therapy (PDT) on human choroidal
neovascularisation (CNV)
Methods-Two patients with recurrences after PDT with verteporfin underwent
surgical extraction of the CNV. Immediately after surgical excision the sub
foveal neovascular membranes were divided for light microscopic and for ele
ctron microscopic processing. For light microscopy tissues were embedded in
paraffin. Sections were stained with haematoxylin and eosin, and the perio
dic acid Schiff (PAS) reaction was performed to determine histological diag
nosis and to ensure tissue quality. For electron microscopy the specimens w
ere fixed in glutaraldehyde and embedded in epoxy resin. Semithin sections
were stained with uranyl acetate and lead citrate and examined with a trans
mission electron microscope.
Results-Light microscopy showed thick fibrovascular membranes in both cases
. On the outer surface remnants of retinal pigment epithelial cells resting
on thickened inner aspect of Bruch's membrane were found. On the retinal s
ide some outer segments were found. The membrane showed areas with irregula
rly shaped vessels. Electron photomicrographs showed occluded vessels withi
n the CNV containing thrombotic masses and/or ultrastructural damage of the
neovascular endothelium. Most of the vessels presented regressive changes
with vacuolisation and fragmentation of the neovascular endothelium accompa
nied by disintegration of the endothelial cell layer. Extravasation of red
blood cells was observed. Occasionally, vessels with normal endothelium con
taining intact red blood cells were observed. Some vessels contained immatu
re endothelial cells. At some locations the retinal pigment epithelium cell
s (RPE) were metaplastic showing highly vacuolised cytoplasm.
Conclusions-These findings suggest that the evidence of fluorescein leakage
from the CNV and enlargement of the neovascular complex following PDT coul
d be related to new vessel growth and recanalisation of occluded vessels. A
dditionally, RPE disturbances were observed in the specimens. This finding
may be related to the original pathology or could indicate that PDT treatme
nt may result in RPE atrophy.