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Flashcards in Cytology in practice Deck (42):
1

Why do cytology?

quick, easy, cheap, non-invasive, low risk, screening tool, can establish a diagnosis or disease process

2

Limitations - cytology

relies on sample quality (collector skill, smear, tissu eexfoliation, site of collection), interpreter of smears, no information about tissue architecture (vs histopathology), diagnostic challenges

3

Histopathology - advantages

more expensive (sterile), slow (48 hr), poor detail for round cell tumours

4

Histopathology - disadvantages

tissue architecture, tumour grading, immunohistochemistry more available.

5

What samples can you take for cytology?

ASPIRATION OR IMPRINTS: superficial masses, LN, organs and deep masses
FLUIDS: body cavity, joints, respiratory space, CSF

6

When to do fine needle biopsy?

solid or fluid filled masses, visual or US guidance, no negative pressure applied to syringe, small guage needle (22-24), insert into mass several times, masses with necrotic centre you must sample the wall not just the centre then use air filled syringe to expel cells onto slide.

7

Distinguish FNA and FNP

FNA = fine needle aspirate. negative pressure applied to syringe. use only if FNB not possible.

FNB = fine needle biopsy, NO negative pressure applied to syringe. first choice method.

8

What makes a smear of a good quality? 3

cells nicely spread out, not ruptured, not just chromatin fibres from nuclei visible.

9

3 goals of smear preparation

thin areas with good cell spread, minimise cell damage, minimise blood content

10

Another name for a touch impression?

Imprint

11

What are imprints good for?

Evaluation of excised tissue or superficial lesions. Made before the tissue is placed in 10% buffered formalin and submitted for histopathology

12

How to make an imprint

Use fresh cute surface of tissue, blot until dry, imprint directly onto glass slide, tissue should be roled agaunst the slide, 4-5 imprints per slide, allow to air dry and then stain.

13

How is fluid collected? 3

With EDTA - clot prevention
sterile pot - bacteriology
fresh - slide preparation (direct smear, line preparation, squash preparation, concentration techniques)

14

What is the most important thing to determine from a cytology smear?

Inflammatory or neoplastic

15

What to determine if lesion is inflammatory

Septic or non-septic

16

What to determine if lesion is neoplastic

Round cell, epithelial or spindle cell

17

Indicators of sample quality - 5

-enough cells to examine
-preservation of cells
-adequate spreading
-representative of the lesion?
-do we expect normal cells/what are normal cells from this area?

18

How to tell if sample is inflammatory?

Dominated by inflammatory cells - neutrophils, eosinophils, lymphocytes, macrophages

19

How to tell if sample is neoplastic?

Sample dominated by tissue cells

20

What if the sample is BOTH inflammatory AND neoplastic?

Need experience/2nd opinion to tell if:
-inflammation with secondary dysplasia OR
-neoplasia with secondary inflammation

21

Indicators of septic inflammation

contains bacteria/organisms, degenerate/lytic neutrophils, bacteria must be intracellular, if extracellular may be contaminants

22

Indicators of non-septic inflammation

no bacteria or organisms seen, neutrophils are non-degenerate, lack of identifiable bacteria and presence of non-degenerate neutrophils

23

Outline degenerative changes in neutrophils 4

-nuclear change
-nucleus swells, loses lobulation and becomes paler (chromatin less condensed)
-secondary to release of bacterial toxins
-if present, consider septic inflammation even if bacteria not seen.

24

What does an increased number of macrophages suggest? What if neutrophils are present too?

-Inflammatory lesion - a granulomatous inflammation (e.g. mycobacterium spp).
-If neutrophils too - pyogranulomatous inflammation (fungal infections).

25

What inflammatory reaction is seen with a FB?

Either granulomatous or pyogranulomatous

26

Describe round cells - 6

individual cells, small to medium size, round to oval cells and nuclei, well defined cell broders, good cell yield

27

List the finite list of Round (discrete) cell tumours - 6

lymphoma, plasmacytoma, histiocytoma, mast cell tumour, transmissible venereal tumour (TVT), (melanoma)

28

Describe epithelial cells

often found in sheets/rafts/clusters, large cell size, cell to cell junctions, oval to angular in shape, round nuclei which are centrally located, cytoplasm often abundant, good cell yield.

29

Examples of epithelial cell tumours

sebaceous, mammary, liver

30

Describe mesenchymal cells

individual cells or clumps, small to medium size cells, spindle to fusiform to stellate, indistinct cell borders, elongated nucleus, poor exfoliation, matrix production (collagen, osteoid).

31

Name for benign epithelial tumour

adenoma

32

Define carcinoma

Malignant epithelial cell

33

Define fibroma

benign mesenchymal tumour

34

What is a malignant mesenchymal tumour called?

fibrosarcoma

35

What does the behaviour of plasmacytoma tumours depend on?

Depends on type

36

What are criteria of malignancy?

Cytoplasmic and nuclear features:
-uniformity vs. pleomorphism (carcinoma, sarcoma)
-monotony (lymphoma)

-nuclear criteria are most reliable
-need at least 3 nuclear criteria of malignancy before calling a tumour malignant

37

Define anisocytosis

variation in cell size

38

Cellular criteria of malignancy 3

anisocytosis, macrocytosis, cell crowding

39

Nuclear criteria of malignancy - 11

anisokaryosis, multinucleation (vary in size, odd numbers of nuclei), macrocytosis, high N:C ratio (in large cells), increased mitotic figures, abnormal mitotic figures, coarse chromatin, nuclear moulding,macronucleoli, varying nucleolar shape and size

40

Important points to remember when submititng samples to the lab - 8

send multiple unstained smears, label slides/tubes, use pencil, signalment, history, important clinical findings, describe location of lesion, duration and rate of growth, previous lesions and diagnosis, current therapy

41

Common problems with cytology samples - 5

formalin fumes (ruins blood smears), refrigerating glass slides (--> shatter), breakage during shipping, lack of freshly made smears, (flies)

42

What are the most common causes of masses/tumours and are easy to identify? 4

lipoma, mast cell tumour, melanoma, follicular cyst

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