Purpose. We reviewed the records of patients with chronic cicatricial disea
se of the conjunctiva for differences in prognosis between clinical and his
topathological subgroups of the disease and in therapeutic options.
Patients. In 30 patients (58 eyes) with an average age of 69 years (52-86)
chronic cicatricial disease of the conjunctiva was diagnosed clinically. On
ly in 22/30 patients conjunctival biopsies could be performed. The correlat
ion of histopathological and immunohistochemical diagnoses with clinical co
urse under systemic immunosuppression was studied.
Results. 15/22 biopsies led to a classification into different subgroups. U
nder systemic immunosuppression disease ceased to progress fora mean time o
f 15 months in 13 of 15 patients with positive biopsies and in 9 of 15 with
out classification. The results after cyclosporine A therapy (4 of 5 patien
ts stabilized after a mean of 27.5 months) and mycophenolate mofetil (8 of
11 patients stabilized at a mean of 7.8 months) were better than those afte
r therapy with dapsone,azathioprine and cyclophosphamide.
Conclusions. Histopathological and immunohistochemical examinations led to
a classification in two-thirds of the patients with clinical aspects of chr
onic cicatricial disease of the conjunctiva. There was no correlation betwe
en different histopathological subgroups, success of therapy and prognosis
of the disease. There is little hope in using new systemic immunosuppressio
n such as cyclosporine A and mycophenolate mofetil.