The Practical Lab - Cytology Flashcards

1
Q

What is cytology looking at?

A
  • fluid (bronchoalveolar lavage, CSF, synovial fluid, body cavities
  • tissue samples(lumps, bumps, lymph nodes)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What characteristics should you note for a lump?

A
  • localisation
  • firm/soft
  • dimensions
  • painful/non-painful
  • ulcerated/non-ulcerated
  • cutaneous/sub-cutaneous
  • adherent/non-adherent
  • how does the aspirate look?
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Why would you do a suction FNA?

A

-for hard, cutaneous or subcutaneous tissue
- on bone lesions
- when non-suction technique is unsuccessful

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

When might you do a non-suction FNA?

A
  • on soft cutaneous or subcutaneous masses
  • lymph nodes
  • vascular lesions/organs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How do you do a suction FNA?

A

draw back on plunger once inside mass, relax plunger then remove

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How do you do a non-suction FNA?

A

use just the needle, draw up air in a syringe, attach needle then push plunger

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

hat other collection methods are there other than FNA?

A

impression smear, scraping, ear swab (imprint then roll on slide), biopsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is malassezia?

A

fungus (yeast) peanut shaped and usually present in slow numbers on normal skin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What should you do after collecting a cytology sample?

A
  • dry quickly with air or hair dryer
  • sample must be completely dry before staining or packaging to send away
    -label smears with pencils
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How would you stain a cytology sample?

A

diff quick

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What other staining can you use other than diff quick?

A
  • giemsa/modified weight
  • methylene blue
  • toluidine blue
  • ziehl/nielsen
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is involved in diff quick staining?

A

solution A - methanol- fixation
solution B - eosin - eosiniphilic (base) staining
solution C - methylene blue - basophilic (acid) staining

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Which stain deteriorates quicker than others?

A

methylene blue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are you looking for under the microscope aat low magnification (10x)?

A
  • cellularity
  • preservation
  • staining
  • haemodilution
  • cell distribution
  • background
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are you looking for under the microscope at high magnification (40x)?

A
  • cellular vs non-cellular elements
  • inflammatory vs neoplastic
  • malignant vs benign
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are you looking for under the microscope at high magnification (100x)?

A
  • presence of cytoplasmic granules
  • nuclear detail
  • presence of pathogens (bacteria, fungi, protazoa)
17
Q

What do neutrophils look like?

A

crispp nuclear outlines with dark purple chromatin, pale clear to slightly eosinophilic cytoplasm

18
Q

What are degenerate neutrophils?

A

neutrophils affected by toxic change

19
Q

What do degenerate neutrophils look like?

A

loss of segmentation, lighter coloured ‘fluffy’ nuclear chromatin and a swollen appearance

20
Q

What do histamine granules look like?

A

tiny purple dots

21
Q

What does a lipoma look like under the microscope?

A

chicken wire