Neoplasia Flashcards

1
Q

How do you classify neoplasms

A
  • on cell origin
    E.g epithelial
  • on tumour behaviour
    E.g malignant
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2
Q

How do you classify tumours

A
  1. Epithelial - carcinoma
  2. Mesenchymal - liposarcoma
  3. Neuroectoderm - astrocytoma
  4. Haemopoietic - lymphoma
  5. Germ cells - teratoma
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3
Q

Benign vs malignant tumour

A
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4
Q

Cell growth of tumour cell

A

See abnormal mitosis in malignant cells

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5
Q

Gross description of tumour

A

Size

Shape

Number

Consistency

Site

Special features

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6
Q

Grading tumours - how it looks

A

Grade 1 - well differentiated

Grade 2 - moderately differentiated

Grade 3 - poorly differentiated

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7
Q

Tumour morphology

A
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7
Q

Tumour staging

A

The extent of the tumour in the body,
How it has spread

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8
Q

What’s does grade 1 squamous cell carcinoma look like

A

Tumour resembles normal squamous epithelium and contains proportion of differentiated keratinocyte-like squamous cells.

Intercellular bridges are always present.

Keratin pearls are frequently found.

Mitoses are scanty.

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9
Q

What does grade 2 squamous cell carcinoma look like

A

Tumour cells exhibits more nuclear pleomorphism.

There is usually less keratinisation.

Increased number of mitoses, including abnormal mitoses.

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10
Q

What does grade 3 squamous cell carcinoma look like

A

Non-keratinsed basal-type cells predominate.

Barely discernible intercellular bridges,
and minimal
keratinisation.

High mitotic rate, including abnormal mitoses.

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11
Q

Effects of benign tumours

A
  1. discomfort
  2. production of active substance, e.g. hormone (thyroid adenoma)
  3. Pressure effect on adjacent tissue, e.g. intracranial or intrauterine
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12
Q

Direct effects of malignant tumours

A

• Pain, rapidly growing infiltrative mass
• Blood loss, ulceration, haemorrhage, anaemia
• Mechanical effect, stenosis or obstruction

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13
Q

What are paraneoplastic syndromes

A

• Paraneoplastic syndromes are symptoms that occur at sites distant
from a tumour or its metastasis.

• Pathogenesis unclear, but symptoms may be secondary to substances
secreted by the tumour or a result of antibodies directed against
tumours that cross-react with other tissue.

• Up to 20% of cancer patients experience paraneoplastic syndromes.

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14
Q

What is tumour grade

A

biological nature of tumor, based on histological analysis: differentiation, mitotic activity, pleomorphism

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15
Q

What is tumour stage

A

extent of tumour: size and spread, after pathological and radiological analysis

16
Q

5 main modes of tumour spread

A

• Local invasion.
• Lymphatic spread.
• Vascular spread.
• Other ways of spread: Transcoelomic spread or Intraepithelial spread.

17
Q

What is local invasion

A

Tumour spread into surrounding tissues by the direct route. Examples: carcinoma of the breast invading overlying skin and
carcinoma of the cervix invading rectum or bladder

18
Q

What is lymphatic spread

A

• Cancer spread via lymphatic vessels
draining the site of primary tumour.

• Neoplastic cells are conducted to local
lymph nodes where they may form
secondary tumours, e.g. breast cancer
spreading to axilla lymph nodes, or
tongue cancer spreading to neck
nodes.

• Form the basis of N (lymph node)

19
Q

What is vascular spread

A

• Tumour spread via the veins
draining the primary site.

• Gut tumours tend to spread via
the portal vein to the liver.

• In the systemic circulation,
neoplastic cells may be trapped
in the lung to form pulmonary
metastases.

• The basis of M staging (metastasis)

20
Q

What is Transcoelomic spread

A

• Tumours can spread across
coelomic spaces, e.g. across the
peritoneal or pleural cavities.

• Carcinoma of the ovary may
spread transcoelomically to
produce large numbers of
metastatic deposits on the
peritoneal surfaces

21
Q

What is intraepithelial spread

A
22
Q

How to use TNM classification to stage tumours

A

T- tumour
N- node
M- metastasis

23
Q

Dysplasia is…

A

Disordered development of epithelium

It may be pre-malignant

24
Q

What are proto-oncogenes

A

• Genes commonly used during normal growth and development.
• Usually under-control.
• Without control, they have the potential to produce neoplasms through
their excessive expression.

25
Q

What are oncogenes

A

• Genes that have made the transition , i.e. activated proto-oncogenes.
• Capable of producing neoplasms.
• Most oncogenes cause unregulated cell growth through promotion of cellular division, which results in further mutations.

26
Q

Conversion of proto-oncogene to oncogene

A

• Overexpression of the gene.
• Amplification of the gene.
• Point mutation in the gene.
• Translocation of the gene to another region with resultant
overexpression of the gene, or resultant production of protein with
oncogenic activity.

27
Q

What are genes p53 and rb1 does

A

They are tumour suppressor genes

28
Q

What does nitric oxide do to vessels

A

Causes vasodilation

29
Q

What mediator causes b cells to plasma cells

A

IL-6