Purpose: To determine which human corneal diseases show similar abnorm
al corneal surfaces, characterized by conjunctival epithelial ingrowth
(conjunctivalization), vascularization, and chronic keratitis (i.e,,
a constellation of signs termed limbal stem cell dysfunction [deficien
cy], which have been noted in experimental rabbit models). Methods: A
total of 134 impression cytology specimens of the perilimbal region co
llected from 1984 to 1994 were reviewed. Limbal deficiency was diagnos
ed if conjunctival goblet cells were found on the corneal surface, Res
ults: Ninety-four patients were found to have limbal deficiency. Categ
ory 1 comprised 53 patients with a clear history showing limbal stem c
ell destruction by chemical/thermal burns, Stevens-Johnson syndrome, m
ultiple surgeries and cryotherapies, contact lens wear, and severe mic
robial keratitis. Patients in category 2 (n = 41), did not have such a
history, but gradual loss of stem cell functions over time was disclo
sed and included diverse causes such as aniridia, multiple endocrine d
eficiencies, neurotrophic keratopathy, peripheral inflammatory keratop
athy or limbitis, and idiopathy. The 40 remaining patients with suspic
ious findings did not have limbal deficiency, Conclusions: Impression
cytology can be used to diagnose and monitor corneal diseases with lim
bal deficiency, which manifest distinct clinical problems and are gene
rally poor candidates for penetrating keratoplasty. The identification
of category 1 diseases allows one to consider limbal (stem cell) tran
splantation for surface reconstruction, The presence of category 2 dis
eases indicates that limbal stem cell functions can be modulated by de
velopmental, hormonal, neuronal, vascular, and inflammatory factors in
the limbal stroma.