The growth of a cholesteatoma requires angioneogenesis in the connecti
ve tissue of the perimatrix. Angioneogenesis is also needed for wound
healing as a host response to tissue injury. Normal wound repair is co
nducted through a wide number of growth factors. Basic fibroblast grow
th factor (b-FGF) plays a pivotal role in wound repair. This cytokine
exerts its effects through stimulation of a wide range of target cells
. B-FGF is chemotactic and mitogenic for fibroblasts, endothelial cell
s and keratinocytes. In addition, b-FGF can stimulate the production o
f collagenase and plasminogen activators to enhance fibroblast prolife
ration and angioneogenesis. Its necessity for normal wound repair has
been confirmed by several workers. Method: In order to demonstrate ang
ioneogenesis in the cholesteatoma perimatrix the distribution of b-FGF
as the pivotal cytokine of the process was investigated in the perima
trix of 18 cholesteatoma specimens. Results: B-FGF could be observed i
n 12 of 18 specimens (66%) in close approximation to histological sign
s of inflammation and wound healing. Areas with b-FGF also exhibited p
roliferation of the covering squamous epithelium. Cholesteatoma matrix
tissue without inflammation or any sign of wound healing did not expr
ess b-FGF (6 of 18). Conclusion: Histological changes and distribution
pattern of b-FGF in the perimatrix of cholesteatoma in the present st
udy indicate that the perimatrix cells and substances of the wound hea
ling cascade may play an important role in cholesteatoma development,
angiogenesis and growth.