Cytology Sample Collection - Ex 6 Flashcards

1
Q

Sample Collection - Solid Mass

A
  1. Aspiration 2. Fenestration 3. Impression smear
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Sample Collection - Fluid-filled Mass

A
  1. Aspiration - direct smear - concentration preparation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Sample Collection - Excised Tissue

A
  1. Imprint - blot tissue thoroughly - roll 2. Swab
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Sample Collection Guidelines

A
  1. Sample multiple areas 2. Aspirate edges of large lesions 3. Do NOT heat fix!! 4. Do NOT expose to formalin!
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Aspiration/Fenestration

A
  • Sterile 22G needle - 6 or 12 cc syringes - Stains - Scope
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

FNA - steps

A
  1. attach needle to syringe and position needle in the mass 2. rapidly pull back several times 3. release pressure and withdraw lesion 4. take needle off –> pull air into syringe 5. reattach needle to syringe and expel air through to push cells onto slide 6. use additional glass slides to smear sample 7. air dry and stain
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

FNF - steps *good for firm, nodular lesions

A
  1. 18 to 20 G needle 2. repeatedly reposition the needle in the mass without withdrawing needle from skin 3. expel cells in the needle hub onto a slide using air-filled syringe 4. use additional slide to smear 5. air dry & stain
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Impression Smear - steps

A
  1. gently press clean glass slide onto the surface of the lesion 2. air dry and stain **good for ulcerated lesion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Fluid-filled lesions

A
  1. perform FNA 2. place portion of fluid into sterile tube for bacti or fungal culture 3. place additional fluid in an EDTA or heparinized tube 4. make direct smear *if cellularity is low - centrifuge and remove the supernatant and smear the cell pellet
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Imprint - steps

A
  1. cut section 2. blot vigorously to minimize blood contamination 3. press onto the slide multiple times
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Artifacts

A
  1. US/lubricant gel - eosinophilic material obscures cells - AVOID at all costs 2. glove powder 3. pollen 4. anucleated squamous epithelial cells - skin surface contaminants - finger prints on slides
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What can damage cells?

A
  • heat fixation - formalin fixation - poor sample handling *cell lysis, samples too thick, or poor staining technique
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Staining - Cytology

A
  1. Romanowski-type stain - diff-quick - extra time in fix for thick samples - send through stains twice if needed 2. Gram stain - only useful to determine if bacteria are Gram-+/- - NOT a ‘cytological’ stain
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Slide Examination

A

* Cellularity - high vs low * Cellular components - inflammation - hyperplasia - neoplasia * Background - blood - protein - broken cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Cytologic Interpretation - Cysts

A

poorly cellular fluid-filled

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Cytologic Interpretation - Hemorrhage

A

blood erythrophagia

17
Q

Cytologic Interpretation - Inflammation

A

purulent pyogranulomatous lymphocytic eosinophilic

18
Q

Cytologic Interpretation - Mixed

A

inflammatory & non-inflammatory cells

19
Q

If a cytologic description does not make your clinical findings…

A

… question it! *small sample, may not represent lesion *consider re-aspiration or biopsy with histopathology

20
Q
A

Gel

21
Q
A

More Gel

22
Q
A

Glove Powder

23
Q
A

Pine Pollen

24
Q
A

Surface Epithelium