Neoplasia Flashcards

Revision

1
Q

What is the definition of cancer?

A

To a pathologist: Uncontrolled cell proliferation and growth that can invade other tissues

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2
Q

What is a tumour?

A

Swelling.
Can be benign or malignant.
May even by inflammatory.
Could be a foreign body.

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3
Q

If a tumour is big, is it more likely to be benign or malignant?

A

Malignant

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4
Q

If a tumour is very big but the skin is intact has it grown quickly or slowly?

A

It is more likely to have grown slowly because the skin is intact. If it had grown quickly the skin wouldn’t have stretched.

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5
Q

What is a neoplasm?

A

The literal translation of neoplasia is new growth.
Not in response to a stimulus (see hyperplasia).
Can be benign, premalignant or malignant. Often used as a clinician code for cancer - remember not true.
The plural of neoplasm is neoplasia.

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6
Q

Where do you get a neoplasm?

A

Anywhere.
Only part of the body not reported to have undergone neoplastic change is the lens of the eye.
Any cell from any organ.
Normal cells.
Epithelium -mucinous, oxyntic cells, smooth muscle, nerves, inflammatory cells, stromal cells, pacemaker cells (interstitial cells of cajal), neuroendocrine cells, blood vessels (endothelium).
Tumours o them all can occur but obviously some are more common than others.

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7
Q

How do you define benign compared to malignant?

A

Difficult to come up with an accurate definition.
Malignant tumours have metastatic potential (metastatic potential reflects the cumulative effect of a wide variety of genetic and epigenetic changes involving tumour cell adhesion, motility, and protease production).
Metastases spread to other sites.
Epithelium has a basement membrane. Malignancy goes beyond basement membrane.

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8
Q

Why is it not as simple as cells being either benign or malignant?

A

Clearly things don’t just all of a sudden become malignant.
There are precursor stages.
This is often the basis of screening programmes.
Precursor lesions:
- Dysplasia
- Metaplasia
- Even hyperplasia

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9
Q

What is the definition of metaplasia?

A

Reversible change from one mature cell type to another mature cell type.

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10
Q

How does metaplasia come about and is it reversible?

A

Metaplasia is not reversal in the appearance of adult cells.
Represents a change in signals delivered to stem cells causing them to differentiate down a different line.
May be in response to cytokines (chemical messengers), growth factors and other chemicals in the cells microenvironment.
Commonly occurs in response to a noxious stimulus.
Squamous epithelium covers your skin and is very resistant to a range of noxious stimuli.
Squamous metaplasia is therefore commonly encountered in response to injury - lung an salivary ducts.

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11
Q

You get a lot of squamous epithelium where?

A
Lung
Bronchial epithelium - cilia allow clearance of mucous etc.
No good with thermal/chemical injury.
Turns to squamous epithelium.
Bladder
Usually transitional epithelium.
Catheter  - creates inflammation.
Epithelium changes to squamous.
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12
Q

Does Hyperplasia require a signal or can it be autonomous?

A

Hyperplasia - the other ‘asia’ associated with cancer.
Can be autonomous and no longer require stimulus.
Basic structure of steroid hormones is shared by cholesterol (obese individuals are at massively increased risk).

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13
Q

Is Dysplasia always in response to a stimulus or is it ever autonomous and how is it graded?

A

Literally it is disordered growth
In abnormal cells, growth is not in response to a stimulus (remember hyperplasia).
No invasion.
Invasion - growth beyond the basement membrane.
Dysplasia - often graded. Low grade most normal. High grade most abnormal and closest to becoming cancer.

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14
Q

Why do we grade dysplasia?

A

We often grade dysplasia because we know it reflects the likelihood of malignancy.
High grade, high risk of becoming a malignancy.
Low grade, low risk of becoming a malignancy.

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15
Q

What is the aim Cervical Screening?

A

Aim is to catch the dysplasia before it becomes malignant.
Forms the basis of smears and previous screening methods.
Detection of disordered growth in the cervix. Aim is to catch dysplasia before it becomes cancer.

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16
Q

What is CIS (Carcinoma-in-situ) and what does it indicate?

A
Carcinoma in-situ.
Dysplasia affecting the whole of the epithelium. Applies to non-glandular epithelium.
Bladder - transitional epithelium.
Squamous epithelium.
Last stage before becoming invasive.
17
Q

What are 8 causes of cancer?

A
Genes
Smoking
Alcohol
UV radiation
Other radiation
Drugs
Infections
Obesity
18
Q

What are the Weinberg Hallmarks?

A
  1. Increase growth signals
  2. Remove growth suppression
  3. Avoid apoptosis
  4. Achieve immorality
  5. Become invasive
  6. Make you blood supply (angiogenesis)
  7. Loss of spell DNA spell checks
  8. Avoid the immune system
19
Q

Why is cancer common in the lungs and oesophagus?

A

Metaplastic tissue is an at risk site for the development of cancer.
Thus, although there is no squamous epithelium in the lung squamous cell cancer is quite common.
Adenocarcinoma (gland forming tumour) is common in the oesophagus despite there being no glandular epithelium in the oesophagus.

20
Q

How do we get cancer?

A

For rare tumours this may be easily answered.

For common tumours it is unlikely that there is only one factor involved.

21
Q

In basic terms how do cancers survive?

A

Cancer is an alteration of normal growth.

Cancers must avoid death and promote survival and growth.