Pathology Flashcards

1
Q

What are the most common lab errors?

a) analytical
b) pre-analytical error
c) post-analytical error

A

b) pre-analytical error

Mislabelling where the specimen and requisition don’t have the same label

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2
Q

Once a specimen arrives to the lab, what is the first step the pathologist takes?

A

Weight and measure its dimensions

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3
Q

Why do we ink margins?

A
  • For orientation and mapping (proximal to distal)
  • You ink all portions that where separated from adjacent tissue, where separation from that plane required a physical act
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4
Q

Positivity of a margin suggests what?

A

Suggests non-resection, and that local control of the tumour is still needed

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5
Q

Do you paint/ink skin?

A

No, because it is in contact with air and was not in contact with adjacent tissue.

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6
Q

What is a positive margin?

A

=Tumour is touching ink

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7
Q

Very low grade tumours, can do a capsular exicision, true or false?

A

True

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8
Q

High grade Sarcoma, can do a capsular exicision, true or false?

A

False,

Do a wide-local excision

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9
Q

What is the goal of processing?

A

To convert a gross specimen into thin cassettes/slides that can examine under a microscope

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10
Q

How thin does a specimen need to be cut into before it can be examined under a microscope?

A

1 to 2 cells thick.

Need a single optical plane

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11
Q

How big is a cell?

A

5 microns

5/1000th of a mm

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12
Q

What instrument is used to cut a specimen into smaller slices?

A

Microtome

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13
Q

Why can’t you cut/linearize a specimen directly with a microtome?

A

It has water in it, that causes surface tension. The tissue cannot be cut or linearized properly.

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14
Q

What are 2 ways to solidify water?

A
  • Freeze water

- Remove water and replace it with another solid

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15
Q

Tissue processing essentially replaces water with what?

A

Parrafin wax

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16
Q

Once a tissue is parrafin wax solidified, is it fixed yet?

A

No

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17
Q

What does a fixative do in fixation?

A

Tissue is killed

Methylated and cross-linked the proteins (denatured them)

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18
Q

What are examples of fixative?

A

Formalin
D5
Alcohol

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19
Q

When can you NOT fix a tissue?

A

When a viable tissue is required for analysis

Ex tissue culture, bacterial culture, gram stain

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20
Q

Does fixation kill DNA?

A

No

only denatures protein

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21
Q

What is tissue fixation?

A

Rendering tissue SOLID and invulnerable to autolysis

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22
Q

What is tissue processing?

A

Rendering tissue solid

solidifying water with paraffin wax, or frozen section

23
Q

Why don’t we do frozen section on every specimen?

A

Tissue distorted and contour/shape is lost.

24
Q

What does “defer to permanent” mean?

A

Distortion artifact of frozen section is too severe and is interfering with safe/accurate diagnosis.

25
Parrafin wax, 2 important properties?
Completely viscous at high temperature | Complete solid at cool temperatures
26
One full gear turn of the microtome gives what thickness of cut?
5 microns
27
H&E stain is essentially what?
A fabric dye
28
Why use H&E stain? i.e. what is histochemistry?
To differentially highlight different elements in a tissue by exploiting their different chemical properties (i.e. nucleic acids vs protein)
29
What molecule a radically different charge properties than any other?
DNA | phosphodiester back bone (tons of negative charge)
30
Cationic dye is what colour? Anionic
Cationic - Blue (DNA) | Anionic - Red (cytoplasm)
31
What are 4 kinds of special stains?
- Histochemistry - Immunohistochemistry - In situ hybridization - Immunofluoresence
32
Name a tumor where cytogenics of the tumour is diagnostic?
Lymphoma (Burkitt's) | 8q14 mic oncogene translocated under immunoglobulin promoter
33
POS may ask about specific translocations associated with certain tumours, true or false?
True
34
Can a karyotype be done on fixed tissue?
Depends on the kind of fixation
35
Why did we start using Karyotypes in medicine? (cytogenics)
The application of cytogenics was first applied in obstretics, for diagnosis of Trisomy disorders.
36
What stage of cell cycle are cells trapped into for cytogenic/karyotype analysis?
Trap them in metaphase
37
Giemsa uses what chemical property to differentiate between structure?
Redox status
38
Giemsa is what kind of stain?
A silver-impregnated stain
39
What is a tissue/tumor of epithelial origin?
Carcinoma
40
What is a tissue/tumor of mesenchymal origin?
Sarcoma
41
What is a tissue that is CD45+ve? | S100 +ve?
Lymphoma
42
Tissue that is S100 +ve?
Melanoma
43
What tumor has almost all cells in S-phase (i.e. is growing so quickly)? What is the problem with that?
Burkitt's lymphoma In S-phase means Tremendous apoptosis --> Tumor lysis
44
What is a sarcoma of skeletal muscle origin called?
Rhabdomyosarcoma
45
What is a vascular sarcoma?
Angiosarcoma
46
List 4 skeletal muscle markers (Histogenesis)
MMMD - Myogensis - Myoglobin - MyoD1 - Desmin
47
List 2 smooth muscle markers
- Actin | - Smooth Muscle actin
48
List 2 neural tissue markers
- S100 | - PgP9.5
49
List 4 Vascular markers
- CD31 - Cd34 - Factor VIII - D240 (lymphatics)
50
What are 6 ancillary studies one can use?
- Electron microscopy - FISH - Conventional Cytogenetics - Flow cytometry - Molecular studies - Microbiology cultures
51
What is the fixative for electron microscopy?
Glutaraldehyde
52
What stain do you use/see on a frozen section?
H&E
53
What is "Tissue Fix"?
Formaldehyde 2-5% | A fixative
54
Histology vs Cytology?
Histology - see the tissue/cell in its 3D architecture | Cytology - individual aggregated disorganized cells