This presentation given by Tracy Stokol, BVSc, PhD and Associate Professor in Clinical Pathology at Cornell University, consists of a review of sample collection, smear preparation and staining of cytology samples. The lecture will conclude with instructions on general slide evaluation for common lesions diagnosed on cytology and clinical cases to practice your skills.
Date: July 2014
Venue: 2014 ASPCA/Cornell Maddie's® Shelter Medicine Conference
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The smear type is not dictated by the type of sample (e.g., fluid, solid tissue aspirate, biopsy).
History details are not required.
They should be keep out of contact with formalin.
Unstained slides are coverslipped.
All of the above.
True
False
You should press the bottom and top slide together.
Slides must be at a 90 degree angle.
You should put your drop of blood or aspirate close to the frosted edge.
A and B.
A, B and C.
Is dictated by the clarity of the sample.
Is dictated by the color of the sample.
Is dictated by the amount of the sample.
Is dictated by the weight of the sample.
All of the above.
Use fresh cut surface to avoid ulcerations.
Blot first for impression smears.
Scalpel blade scrapings are hard to stain adequately.
All of the above.
A and B.
True
False
Identify good areas to look at (i.e., cells are well spread and well stained).
Initially identify anything that appears strange.
Take a closer look at unusual areas on the slide.
Visualize cells with oil immersion.
A and B.
Further evaluate areas that appear strange.
Visualize cells with oil immersion.
Identify blood, inflammation and tissue cells.
All of the above.
None of the above.
Erythrocytosis.
Bacteriopsonin.
Cell lysis.
Anti-mortem: clostridial overgrowth, exfoliation of mesothelial cells, autolysis.
All of the above.
Inadequate staining (insufficient time, smear too thick)
Time for the stained sample to air dry
Diff-quick staining
Impression smears of fresh cut samples
All of the above
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