W. Sekundo et P. Seifert, HYDROXYAPATITE ORBITAL IMPLANT - A LIGHT-MICROSCOPIC AND ELECTRON-MICROSCOPIC AND IMMUNOHISTOCHEMICAL STUDY, Ophthalmology, 105(3), 1998, pp. 539-543
Objective: This study aimed to characterize the constituents of the in
grown host tissue in explanted orbital coral spheres by means of light
electron microscopy and immunohistochemistry and to compare findings
at different intervals after implantation, Design and Methods: A micro
scopic retrospective laboratory study of three explanted coral spheres
from three different patients was undertaken. The first specimen was
an infected hydroxyapatite orbital implant, which was removed after 18
.5 months and processed for standard light microscopy and transmission
electron microscopy. Immunohistochemistry was performed using vimenti
n, actin, CD-68, and CD-34 marker, Two other explanted spheres (after
3 weeks and 2.5 months) were examined by light microscopy only, becaus
e no fibrovascular ingrowth could be detected, Results: On light micro
scopy, the pores of the first coral were filled entirely with the fibr
ovascular tissue, A basophilic line reminiscent of calcium deposition
was seen along hydroxyapatite spicules, where it often was associated
with newly formed bony lamellae, Similar lines were seen partially in
the 2.5-month specimen but not in the 3-week specimen, Immunohistochem
istry of the first specimen enhanced visualization of the capillary ne
twork when the CD-34 marker was used. The fibrovascular tissue was uni
formly vimentin-positive and partially actin-positive. On transmission
electron microscopy, typical fibroblasts and myofibroblasts were obse
rved, The latter were separated by thin sheets of banded collagen and
formed pseudoepithelial structures, Proliferating vessels often showed
high endothelial cells, Conclusions: The fibrovascular ingrowth conta
ins not only vimentin-positive regular fibroblasts but also actin-posi
tive myofibroblasts. Interaction between the invading tissue and hydro
xyapatite structures leads to long-term ossification.