G. Bang et al., DNA FLOW-CYTOMETRY OF RECLASSIFIED SUBTYPES OF MALIGNANT SALIVARY-GLAND TUMORS, Journal of oral pathology & medicine, 23(7), 1994, pp. 291-297
Malignant salivary gland tumors are rare, constitute a heterogeneous g
roup and are often difficult to diagnose histologically. This is borne
out by the fact that in the present study 43.2% of 118 salivary gland
tumors originally diagnosed as mucoepidermoid, acinic cell and adenoi
d cystic carcinomas had their original diagnosis altered upon reclassi
fication. Patients with confirmed adenoid cystic carcinomas had a much
worse prognosis than those with mucoepidermoid and acinic cell carcin
omas. DNA flow cytometry showed that very few of the above mentioned t
hree types of malignant neoplasms revealed aneuploid DNA stemlines, in
dicating that this is not a relevant prognostic tumor marker within th
e groups. However, several of the tumors that had their diagnosis chan
ged, mostly to undifferentiated adeno- or squamous cell carcinomas, sh
owed aneuploid DNA stemlines. The survival lime of patients with aneup
loid tumors was considerably reduced compared to those with diploid tu
mors. Among confirmed acinic cell, mucoepidermoid and adenoid cystic c
arcinomas the S-phase fraction was a significant prognostic factor, as
it was among all tumors examined. This indicates that DNA aneuploidy
and S-phase fractions are potential prognostic factors for malignant s
alivary gland tumors, and that DNA flow cytometry may assist the chara
cterization of such tumors.