Oncology 1 Flashcards

1
Q

Stages of cancer diagnostics

A
  1. diagnosis- what is it?
  2. Staging- How far has it gone?
  3. Treatment- What to do with it?
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2
Q

Potential diagnostic tests

A
  1. FNA
  2. Biopsy
  3. Bone marrow sampling
    4.Clonality test
  4. Flow cytometry
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3
Q

Fine needle aspirate

A

First diagnostic test that should be conducted
-use 22-23G needle
-can use ultrasound guided

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4
Q

Mast cell tumours and FNA

A

-release histamines as soon as they are poked with FNA technique
=brusing, reaction= give antihistmines immediately

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5
Q

Cytology tips

A
  1. Are there nucleated cells?
  2. Is the population uniform?
  3. What type of cells are they?
  4. Malignancy criteria?
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6
Q

Cancer cell types

A
  1. Epithelial
  2. Mesenchymal
  3. Round cell tumor
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7
Q

Epithelial tumours

A

-Arise from the cell of surface layer (organs, glands, skin)
=adenomas and carcinomas

-will be clustered together (“want to hold hands”)

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8
Q

Mesenchymal tumors

A

-will be spread out (“no tight connections between cells”)
-tail present

=sarcomas (from fibrous tissue, nerves, etc.)

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9
Q

Round cell tumors

A

-Cancers of blood
-Round, individualized (don’t need to be clumped together)

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10
Q

Round cell tumors DDx

A

-lymphoma
-Mast cell tumor
-Histiocytic sarcoma
-Histiocytoma
-Plasma cell tumour
-Melanoma
-Transmissible venereal tumour

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11
Q
A

Mesenchymal tumour

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12
Q
A

Round cell tumour
-this one is mast cell tumour (see granules)

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13
Q
A

Round cell tumor

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14
Q
A

Lymphoma

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15
Q
A

Mast cell tumours

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16
Q
A

Histiocytic sarcoma

17
Q
A

Plasma cell tumours

18
Q
19
Q

Histopathology

A

Collect tissue biopsy/sample of the mass
-can tell us about the border and invasiveness of the tissues

20
Q

Adenoma vs adenocarcinoma in histopathology

A

Adenoma= very clear border

Adenocarcinoma= no clear border, invasive into normal tissues

21
Q

Potential tissue biopsy methods

A
  1. Tru-cut- used to prevent bleeding
  2. Punch- superficial
  3. Wedge- when can’t do punch or when tumor is large
  4. Excisional- used when tumour is small
22
Q

When should you do a biopsy?

A

-When differential diagnosis makes sense
-If the result will change the case management

23
Q

Biopsy for plasma cell tumors or histiocytoma?

A

Excise immediately

24
Q

Biopsy for histiocytic sarcoma soft tissue sarcoma, hemangiosarcoma?

A

Treat differently

25
Q

Parts of a histopathology report

A
  1. Diagnosis
  2. Grade, Mitotic count
  3. Margins
26
Q

What should be the next step if results do not fit?

A

Ask for a second opinion
-See major clinical decision 17-39%
-See minor clinical decision= 14-21%

27
Q

Immunohistochemistry (IMC)

A
  1. Diagnostic confirmation
  2. Prognosis
28
Q

Cancers appearing on bloodwork, not as a mass

A

May see cytopenia, increased cell count, circulating atypical cells, monoclonal gammopathy

29
Q

Bone marrow sampling

A

Use needles under GA/sedation and gain cavity
-common in humerus, ileus, ileus to wing

30
Q

Lymphocytes- Neoplastic vs Reactive

A
  • Makes it hard to differentiate
    -cancel out with either PCR or flow cytometery
31
Q

PCR

A

Lymphoma cells, Reactive lymphocytes and non-lymphatic cells have different bands appearing on PCR

32
Q

Cell markers for PCR

A

B cell= Ig

T cell: TCR

33
Q

Lymphoma is…

A

monoclonal

34
Q

Reactive lymphocytes

A

Polyclonal cells

35
Q

Flow cytometery

A

*Used for lymphocytic cancers
1. lymphocytes in fluid
2. When cell passes through tube, they can be grabbed

**cells must be alive

36
Q

Cancer screening

A

Cancer mutation genes leak contents into the blood and tests can detect their presence