Image analysis and flow cytometric DNA studies of benign and malignant body cavity fluids: Reappraisal of the role of current methods in the differential diagnosis of reactive versus malignant conditions
O. Lazcano et al., Image analysis and flow cytometric DNA studies of benign and malignant body cavity fluids: Reappraisal of the role of current methods in the differential diagnosis of reactive versus malignant conditions, MOD PATHOL, 13(7), 2000, pp. 788-796
Citations number
43
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Cytologic examination of body fluids is commonly performed in the clinical
laboratory. Determination of the presence of malignancy may sometimes be di
fficult. In this study, we prospectively studied 60 body fluids with a pane
l of antibodies, including MOC-31, epithelial membrane antigen, carcinoembr
yonic antigen, B72.3, keratin, desmin, and CA-125. DNA and S-phase studies
were performed both by now cytometry and image analysis. Thirty-seven fluid
s were classified as benign and 23 were classified as malignant. The sensit
ivity of the antibodies for identification of carcinoma in descending order
of percentage detection rate were MOC-31 (95%), epithelial membrane antige
n (93%), B72.3 (84%), and carcinoembryonic antigen (80%). Desmin stained me
sothelial cells in all cases. CA-125 gave similar results but was less spec
ific. Flow cytometry detected 14 of 20 malignant fluids and image analysis
17 of 23 by identifying an aneuploid population. Benign reactive mesothelia
l cells were not aneuploid. Tetraploidy due to reactive mesothelial cells w
as found in 9 of 37 body fluids. Their S-phase fraction was low (average, 3
.2%). Tetraploidy in malignant cells was distinguished from the reactive me
sothelial cells by high S-phase (average, 25.95). S-phase had some use as a
discriminating factor, because no benign reactive cases had more than 17%.
However, 7 of 23 malignant cases had a value below 17%. DNA analysis by im
age was more sensitive the and specific than now. Either may be used when i
mmunocytochemistry is nondiagnostic or cannot be performed.