Abstract (EN):
Background: Special stains to demonstrate microorganisms or intra- and extracellular substances have not been evaluated in detail regarding their applicability and usefulness in destained cytologic specimens. Objectives: The aim of this study is to compare the results of routine special stains on destained slides previously stained with Hemacolor and on fresh (unstained) specimens. Methods: Archival Hemacolor-stained fine needle aspirate specimens of inflammation with infectious agents ( bacterial, mycobacterial, and fungal infections), neoplasia ( melanoma, myxosarcoma, and mammary adenocarcinoma), and hemorrhage ( pericardial effusion) from 14 dogs and 7 cats were selected. Cells in a minimum of 4 fields were photographed and 5 slides from each case were then destained by different methods ( alcohol acid or microwave). Seven special stains were applied selectively to the destained slides, depending on the cytologic findings: periodic acid Schiff, Grocott-Gomori methenamine silver, Gram's, Ziehl-Neelsen, Alcian blue, Fontana-Masson, and Prussian blue. The same fields were rephotographed and 2 observers evaluated the slides qualitatively, with comparison to fresh cytologic specimens from similar lesions. Results: Special stains applied to destained slides demonstrated the expected cellular and extracellular material or organisms independent of the destaining method. Staining intensity, nonspecific staining ( background), cell morphology, and nuclear counterstaining results were similar to those of special stains applied to fresh unstained slides. Conclusions: Destaining does not appear to affect the results of routine special staining for cytologic specimens. Destaining before special stains may be a valuable diagnostic strategy when few slides are present or only stained slides are available.
Language:
English
Type (Professor's evaluation):
Scientific
Contact:
rmarcos@icbas.up.pt
No. of pages:
9