E. Chrysomali et al., BENIGN NEURAL TUMORS OF THE ORAL CAVITY - A COMPARATIVE IMMUNOHISTOCHEMICAL STUDY, Oral surgery, oral medicine, oral pathology, oral radiology and endodontics, 84(4), 1997, pp. 381-390
To determine if immunohistochemistry can be used as adjunct to the dia
gnosis and classification of oral benign neural tumors, we stained 77
neurally differentiated tumors with a panel of neural-associated antib
odies (S-100 protein, CD57, epithelial membrane antigen, factor XIIIa,
CD34; CD68, collagen IV). Using standard histologic criteria, we iden
tified 13 schwannomas, 16 neurofibromas, 23 traumatic neuromas, 16 pal
isaded and encapsulated neuromas, and 9 granular cell tumors from arch
ived oral pathology specimens. Silver stains showed that neurofibromas
, traumatic neuromas, and palisaded and encapsulated neuromas consiste
ntly contained axon filaments. Although all neural tumors contained S-
100-positive cells, schwannomas and palisaded and encapsulated neuroma
s contained the most. All tumors expressed CD57; traumatic neuromas we
re stained intensely and the others stained weakly. The consistent epi
thelial membrane antigen capsular staining of schwannomas and the abse
nce of factor XIIIa-positive dendritic/spindle cells helped distinguis
h these tumors from others. Many CD34-positive cells were found in sch
wannomas, and few were found in palisaded and encapsulated neuromas. V
ariable numbers CD68-positive cells were seen in all neural tumor type
s; some of these cells appeared to be macrophages and mast cells, but
many were thought to be Schwann cells expressing this antigen. Collage
n IV staining, apparently representing basement membrane, was generall
y a feature of all benign neural tumors. The immunophenotype of the gr
anular cells of the GCTs was S-100+, CD57+, and collagen IV+ supportin
g the putative neural origin of these tumors. We conclude that neural
origin/differentiation of a connective tissue tumor can be confirmed w
ith stains for S-100 protein, epithelial membrane antigen, CD57, and c
ollagen IV. Staining patterns and intensities associated with the pane
l of antibodies tested can be useful in tumor classification.