Malignant cells in fine needle aspirates possess a cell surface protease wh
ich can be targeted with fluorescent affinity probes. Cells with active GB
exhibit cell surface fluorescence when stained with such affinity probes. T
he nuclei of all cells on the slides can be counterstained with a nuclear f
luorescent stain. Malignant cells are then located by their cell surface fl
uorescence and their diagnosis confirmed by examining their fluorescent nuc
lei. Normal cells and benign cells exhibit no cell surface fluorescence and
can be ignored This technique can be used to rapidly select cells of cytol
ogical interest in FNA samples obtained routinely and might be adapted for
automated screening of FNA.