grading, staging and classification Flashcards

1
Q

why classify tumours?

A

because tumours differ in:

  • cell origin and therefore distribution
  • behaviour

helpful in clinical presentation, prognosis and treatment

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2
Q

tumour grading

A

is a measure of the RATE of tumour growth based on histology

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3
Q

what are the 3 different factors taken into account when grading breast tissue

A
  • differentiation
  • nuclear changes
  • mitotic activity
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4
Q

tumour staging

A

is the measure of the EXTEND of tumour based on clinical, radiological and pathological features

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5
Q

Difference between grading and staging

A

Rate x Duration = extend

grading = rate of growth
staging = extend of growth
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6
Q

TNM staging

A
T = extend of tumour
N = lymph nodes involved
M = metastasis
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7
Q

spread of cancer

A
local spread 
&
metastasis 
-lymphatic spread
- venous spread
- serosal cavities
- nerves
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8
Q

carcinomas

A
  • most common malignant tumours
  • cancers originating from epithelial tissues
  • preceded by in situ growth phase
  • cytokeratin positive
  • spread to lymph nodes, bone, viscera
    treatment mainly surgical
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9
Q

spread to bone

A
  • pathological fracture
  • hypercalcaemia
  • pain
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10
Q

benign epithelial tumours

A
  • adenomas, in glands
  • morphology (regular tight packed cells)
  • some are premalignant
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11
Q

Melanocytic tumours

A

common tumours of the skin, also other sites
- benign (Naevi) and malignant (melanoma)
- arise during embryogenesis from the neural crest
- can define in situ phase for melanoma (unlike CT tumours)
- spread via lymphatics and blood stream
- morphology = cytokeratin negative, S100 positive
treatment mainly surgical

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12
Q

connective tissue tumours

A
  • cannot define in situ pahse
  • spread via blood stream, mainly to lungs
  • sarcomas rare, benign tumours common
  • mainly cytokeratin negative
  • spindle shape under microscope
    treatment = surgery + radiation + chemotherapy
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13
Q

lymphomas

A
  • all malignant
  • no in situ phase
  • spread to other lymph nodes
  • cytokeratin negative
  • leukocyte common antigen positive
  • can be Hodgkin’s or non-Hodgkin’s, and B cells
    treatment = chemotherapy + radiotherapy
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14
Q

Hodgkin’s lymphoma

A

characterized by a multinucleated cell called:

reed-Sternberg cell

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15
Q

Non-Hodgkin’s lymphoma

A

small cell = low grade
-go for a long time, usually incurable

large cell = high grade
- some can be treated and cured by chemotherapy

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16
Q

Leukaemia

A
  • uncommon
  • only malginant type
  • no in situ phase
  • bone marrow
    treatment = chemotherapy
17
Q

the most aggressive cancers present with

A

undifferentiated
poorly differentiated
anaplastic (de-differentiated)
pleomorphic (very inrregular nuclear)

18
Q

immunohistochemistry

A
  • cytokeratin = carcinoma
  • leukocyte common antigen = lymphoma
  • S100 = melanoma