Page 24 - Differential Diagnosis in Small Animal Cytology, The Skin and Subcutis
P. 24

Collection, Preparation

  VetBooks.ir   2               and Staining of Cytology

                                Specimens







             2.1  Materials


             •	  Needles (21–25G) and syringes (2–10 ml) for fine-needle sampling of cutaneous and
                   subcutaneous masses with/without aspiration.
             •	  Cotton swabs, ideally dampened with saline, for swab sampling.
             •	  Glass slides, possibly with frosted end for ease of labelling and identification.
             •	  Plain and EDTA tubes for fluid specimens (e.g. cystic, fluid-filled lesions, abscesses, etc.) for
                 culture and cytology, respectively. The EDTA sample is not suitable for culture, due to its
                 bacteriostatic effect.
             •	  Slide holders to protect smears from breakage when sent to an external laboratory for evaluation.

             2.2  Sampling Techniques


             Fine-needle sampling with aspiration
             •	  Advantages
                 Suitable for sampling most skin lesions, especially those with poor tendency to exfoliate
                 (e.g. mesenchymal proliferations).
             •	  Disadvantages
                 The excessive negative pressure applied during the process may cause cellular damage, espe-
                 cially of more fragile cell types (e.g. lymphoid cells). Excessive haemodilution of the sample
                 may also occur.
             •	  Technique
                 Connect the needle to the syringe. Insert the needle within the mass. Apply suction and
                 redirect the needle multiple times. Discontinue suction before withdrawal. Detach the syr-
                 inge and draw in some air. Reattach the syringe to needle and expel the sampled material
                 on to labelled glass slides.
             Fine-needle sampling without aspiration
             •	  Advantages
                 Suitable for sampling skin lesions with good tendency to exfoliate. This technique better
                 preserves the morphology of fragile cells and minimizes blood contamination.
             •	  Disadvantages
                 May yield an insufficient cell harvest from poorly exfoliative masses.
             •	  Technique
                 Insert the needle within the mass and re-direct it multiple times in different areas of the
                 lesion. Withdraw the needle, attach the syringe containing some air and expel the material
                 on to labelled glass slides.


             © Francesco Cian and Paola Monti 2019. Differential Diagnosis in Small Animal Cytology    11
             (F. Cian and P. Monti)
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