tumour pathology Flashcards

1
Q

what is cancer the homeostasis of?

A

cancer is the homeostasis between cell accumulation by proliferation and cell death, (less cell death, more proliferation)

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2
Q

what is a tumour?

how many cell types are involved within a tumour?

what does “cancer growth is autonomous to themselves” mean?

A
  • a tumour is a neoplasm - “New growth”
  • it is usually just one cell type with supporting tissue structures
    • Neoplastic cells
    • Stroma “normal-like cells” (connective tissue, fibroblasts, blood vessels, immune cells)
  • cancer growth is autonomous to themselves, meaning:
    • Response to physiological stimuli lost or abnormal, allowing unregulated growth
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3
Q

what is the trend between new number of cases of cancer and age?

A

number of new cases of cancer increase with age

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4
Q

what are the top 5 most common cancers?

A
  1. breast
  2. prostate
  3. lung
  4. bowel
  5. skin

most common cancers arise from the epithelial component of the organ system

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5
Q

what do neoplastic cells do?

A

neoplastic cells are not good neighbours, as they affect the tissue locally and distally

  • they are disruptive to the environment
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6
Q

what are the 6 hallmarks of cancer?

A
  1. evading apoptosis
  2. self-sufficiency in growth signals (don’t require any help to grow)
  3. insensitivity to anti-growth signals
  4. tissue invasion and metastasis
  5. limitless replicative potential
  6. sustained angiogenesis
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7
Q

what are 5 characteristics of benign tumours compared to 5 characteristics of malignant tumours

A

benign:
1. well circumscribed
2. slow growth
3. no necrosis
4. non-invasive
5. no metastasis

malignant:
1. poorly circumscribed
2. rapid growth
3. often necrotic
4. invasive
5. metastasis

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8
Q

describe the clinical relevance of benign tumours?

how do they cause disregulation of the local environments?

A
  • Benign tumour (not always clinically benign)
    • Does not invade surrounding structures
    • Does not metastasise
    • Not always clinically benign as they may (cause disregulation of the local environment):
      • have space occupying effects
      • Obstruction
      • Epilepsy
      • Conduction abnormalities
      • cause haemorrhage
      • Pulmonary
      • Gastrointestinal
      • affect hormone production
      • Pituitary
      • Adrenal
      • Endocrine pancreas
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9
Q

describe the clinical relevance of malignant tumours?

what are 4 ways a malignant tumour can spread?

A
  • Malignant tumour - secondary growth of cancer cells at a site distant to the original tumour
    – Invades
    – Metastasises
    • A colony of malignant cells established at a point distant from the original tumour
    how it can spread:
    1. Directly invade locally (‘cancer the crab’)
    2. Via the lymphatics
    3. Via the bloodstream (haematological route)
    4. Through body cavities (transcoelomic route)
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10
Q

seed and soil:
how do tumours metastasise in different manners?

A
  • Tumour cells don’t all behave the same
  • Not all tumours metastasise in the same manner/with the same distribution: patterns of spread (epithelial derived cancers and where they usually metastasise to)
    • Prostate to bone
    • Lung to brain, adrenals
    • Breast to lung, liver, bone, brain
    • Ovary to peritoneal cavity
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11
Q

list and define some names of macroscopic features of cancers:

A
  1. sessile (grow more locally)
  2. polyps (more on surface of a cell layer)
  3. papillary (gut lining potentially, into the lumen)
  4. fungating (invades int tissue area where they arised from)
  5. ulcerating (necrotic damage)
  6. annular (ring structure within lumen structure or blood vessel)
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12
Q

list some macroscopic features of benign tumours:

A

macroscopic features of benign tumours:
1. intact surface
2. exophytic growth
3. homogeneous cut surface
4. circumscribed or encapsulated edge

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13
Q

describe 6 microscopic features of each benign and malignant tumours:

A

microscopic features: benign and malignant

benign:
- Resemble tissue of origin
- Well circumscribed - defined borders
- Well differentiated
- Minimal nuclear pleomorphism - nuclei look normal
- Mitotic figures normal (no cells trying to break into 3 instead of 2)
- No necrosis

malignant:
- Variable resemblance - dont look like tissue
- Poorly circumscribed - no boundaries
- Variable differentiation - dont look like differentiated tissue organ
- Variable pleomorphism may be anaplastic
- Mitotic figures abnormal (tissue trying to break into 3 rather than 2)
- Necrotic

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14
Q

what are cytological features of cells?

describe 5 cytological features of malignancy:

A

cytological features are nuclear changes seen within the structure and function of and animal cells

  • High nucleo-cytoplasmic ratio - high amount of nucleus, lower amount of cytoplasm
  • Nuclear hyperchromasia - nucleus appears darker
  • Nuclear pleomorphism - nucleus appears abnormal in shape and size
  • Abnormal chromatin structure
  • Abnormal mitotic figures
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15
Q

describe how tumour growths are ‘graded on a microscopic histological level

describe what each grade means (1-4)

A

grade is the microscopic histological (histogenic classification) level - grade

  • Resemblance to tissue of origin - differentiation (how similar/different do they look to the tissue of origin)
  • Degree of resemblance to tissue of origin allows GRADING - Determined histologically
  • Grade correlates broadly with clinical behaviour
  • Precise classification important for planning treatment
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16
Q

what are 4 places blood can transport malignant tumours to?

A

blood can spread to:

  • liver (haematogenous spread)
  • bowel cancer
  • peritoneum (transcoelomic spread)
  • lymph nodes (lymphatic spread)
17
Q

what does each letter stand for in TNM staging when classifying the spread of cancer?

A

TNM staging:

T - tumour size

N - Degree of lyph node involvement

M - extent of distant metastases (distance spread)

this is important involving the treatment of patient

18
Q

in Dukes’ staging system for colorectal cancer, the stages of spread are A, B, C, D - describe each stage

A
  • A - confined to bowel wall
  • B - through bowel wall but no lymph node involvement
  • C - lymph nodes involved
  • D - distant spread
19
Q

nomenclature - naming systems of the cancers:

what do all cancers end in?
what are two things benign epithelial tumours can be?
what do benign tumours begin with?
what are carcinomas?
what are sarcomas?

A
  • All end in –oma
  • Benign epithelial tumours are either papillomas or adenomas
  • Benign connective tissue tumours begin with term denoting cell of origin e.g. lipoma (fat cell component)
  • Malignant epithelial tumours are carcinomas
  • Malignant connective tissue tumours are sarcomas
20
Q

what are the 3 major tumour categories?

A

major tumour categories

  • Epithelial origin (papillomas/adenomas/carcinomas)
  • Connective tissue origin (mesenchymal) (sarcomas)
  • Lymphoid / haematopoetic origin
21
Q

describe epithelial tumours

A
  1. Epithelial Tumours:
  • Benign
    – Papilloma (squamous, transitional)
    – Adenoma
  • Malignant
    – Squamous cell carcinoma
    – Transitional cell carcinoma
    – Adenocarcinoma
  • May be associated with a non-invasive precursor
    – Carcinoma in situ (tumours which are benign but are able to progress to malignant cancers
    – Intraepithelial neoplasia (example of above, in prostate cancer)
    • not usually seen in sarcomas
22
Q

describe mesenchymal tumours

A
  • Benign
    – Lipoma
    – Haemangioma etc
  • Malignant
    – Liposarcoma
    – Haemangiosarcoma etc
  • Not usually associated with a non-invasive precursor
23
Q

list examples of miscellaneous tumours

A
  • Melanoma - mesenchymal origin
  • Lymphoma - e.g leukemia
  • Teratoma
  • Embryonal tumours (‘blastomas’) - form in utero during foetal developments
  • Carcinoid tumours
  • Cysts
24
Q

what is a teratoma?

what do teratomas contain?

what is the origin of teratomas?

what forms do they come in?

A
  • a teratoma is an unusual tumour
  • a teratoma contains elements of all three embryonic germ cell layers
  • it is of a germ cell origin
  • occurs in both benign and malignant forms:
  • Ovarian teratomas – almost always benign
  • Testicular teratomas – more often malignant