1: Cellular Pathology of Cancer Flashcards

1
Q

Metaplasia

A
  • A reversible change in which one adult cell type (usually epithelial)is replaced by another adult cell type
  • Adaptive (e.g. to change in pH, reverts when the circumstances change)
  • e.g. columnar epithelium to squamous
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2
Q

Dysplasia

A
  • an abnormal pattern of growth in which some of the cellular and architectural features of malignancy are present
  • pre-invasive stage with INTACT BASEMENT MEMBRANE
  • this is the step between normal cells and cancerous cells (normal epithelium becomes dysplastic before it becomes cancer)
  • increased nucleus-cytoplasmic ratio
  • If we can diagnose “cancer” at the stage of dysplasia it is easy to treat and treatment is 100% effective because no spread (INTACT BM)
  • loss of architectural orientation
  • loss in uniformity of individual cells
  • nuclei: hyperchromatic, enlarged
    mitotic figures: abundant, abnormal, in places where not usually found
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3
Q

Where is dysplasia common and what causes it?

A
CERVIX - HPV infection
BRONCHUS - Smoking
COLON - UC
LARYNX - Smoking
STOMACH -Pernicious anaemia
OESOPHAGUS- Acid reflux
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4
Q

Dysplasia - low grade and high grade

A
  • previously there was also moderate
  • low grade: risk of progresion is low, more likely to reverse easily
  • high grade: less likely to reverse spontaneously, high risk of progression
  • a high grade slide may be darker because the nucleocytoplasmic ratio is higher and the cells appear darker.
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5
Q

Neoplasia, Tumour, Malignancy

A

An abnormal, autonomous proliferation of cells unresponsive to normal growth control mechanisms

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6
Q

What are the features of benign tumours?

A
  1. do not invade do not metastasise
  2. encapsulated (if you can move the mass around i.e. it is not attached to skin or muscle it is a good sign)
  3. usually well differentiated
  4. slowly growing
  5. normal mitoses

=> the first one is key, it is functional; the first one is absolute, the other ones are just characteristics how we recognise benign tum ours.

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7
Q

Are benign tumours alsways harmless?

A

NO!

  • their location is also very important; also whether they secrete anything.
  • i.e. in the Brain
    • in the meninges, it may cause hydrocephalus due to blocking of CSF flow between the lateral ventricles and the 3rd ventricle. This is very serious and could kill you.
    • i.e. pituitary tumours may cause visual defects as well as secretion of hormones
    • Secreting something dangerous: Insulinoma
  • can get infected, cause bleeds, rupture, torts

=> adenomas are benign but not necessarily good.

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8
Q

What may make a benign tumour fatal?

A
  • In a dangerous place: meninges, pituitary
  • Secretes something dangerous: insulinoma
  • Gets infected: bladder
  • Bleeds: stomach
  • Ruptures: liver adenoma
  • Torts (twisted): ovarian cyst
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9
Q

What are characteristics of malignant tumours?

A
  1. invade surrounding tissues
  2. spread to distant sites
  3. no capsule
  4. well to poorly differentiated
  5. rapidly growing
  6. abnormal mitoses

=> the first 2 are about behaviour. The other 4 are how we recognise them.

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10
Q

What is a metastasis?

A
  • A metastasis is a discontinuous growing colony of tumour cells, at some distance from the primary cancer
  • makes local treatment impossible / not enough
  • These depend on the lymphatic and vascular drainage of the primary site
  • Lymph node involvement has a worse prognosis
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11
Q

Where do testicular cancer metastasise?

A
  • aortic lymph nodes
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12
Q

Benign and malignant tumours are distinguished from each other by all of the following except:

  1. Degree of differentiation
  2. Speed of growth
  3. Capsulation
  4. Invasiveness
  5. Site
A
  1. Site
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13
Q

Well differentiated tumours are characterised by all of the following, except:

  1. A small numbers of mitoses.
  2. Lack of nuclear pleomorphism
  3. A high nuclear-cytoplasmic ratio.
  4. Relatively uniform nuclei
  5. Close resemblance to the corresponding normal tissue
A
  1. A high nuclear-cytoplasmic ratio.
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14
Q

What is nuclei polymorphism?

A

Nuclei look different from one another

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15
Q

What are benign epithelial tumours called?

A
  • Of surface epithelium = PAPILLOMA
    (e. g. skin, bladder)
  • Of glandular epithelium = ADENOMA
    (e. g. stomach, thyroid, colon, kidney, pituitary, pancreas)
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16
Q

What is a carcinoma?

A

A malignant tumour derived from epithelium

17
Q

What are the different types of carcinomas?

A
  • squamous cell
  • adenocarcinoma,
  • transitional cell
  • basal cell carcinoma

=> type of cell it is derived from.

18
Q

Where are transitional cells found?

A
  • Transitional cells are able to change shape and stretch.
  • They make up the lining of the renal pelvis, ureters, bladder and urethra.
  • The lining of these organs needs cells that can stretch to expand when urine is stored in or flows through them.
  • transitional cell carcinoma exists
19
Q

What is a benign tumour of bone and a malignant tumourr of bone called?

A
  • osteoma (b)

- osteosarcoma (m)

20
Q

What is a sarcoma?

A

A malignant tumour derived from connective tissue (mesenchymal) cells

21
Q

Different types of sarcomas + their benign correspondents?

A
  • Fat = LipoSARCOMA (vs. lipoma)
  • Bone = OsteoSARCOMA (vs. osteoma)
  • Cartilage = ChondroSARCOMA (vs. enchondroma?)
  • Muscle
    - striated = RhabdomyoSARCOMA,
    - smooth = LeiomyoSARCOMA (vs lyomyoma)
  • Nerve sheath = Malignant Peripheral Nerve Sheath Tumour
22
Q

What are the tumours affecting white blood cells?

A

Leukemia and Lymphoma

23
Q

Leukemia and Lymphoma

A
  • Tumours of white blood cells:
  • Leukaemia a malignant tumour of bone marrow derived cells which circulate in the blood (Leukemia is seen in blood)
  • Lymphoma is a malignant tumour of lymphocytes (usually) in lymph nodes -> lymphomas are tissue based (you see them in lymph nodes, spleen, tonsils)
  • however, there are many exceptions (and overlaps) of leukemia and lymphoma (this is just how they USUALLY behave)
24
Q

What is a teratoma?

A
  • A teratoma is a tumour derived from germ cells, which have the potential to develop into tumours of all three germ cell layers:
    • ectoderm,
    • mesoderm,
    • endoderm
  • most common in testes and ovaries (where germ cells are found)
  • mature adult type tissues in a tumour (e.g. skin, hair etc.)
25
Q

Teratomas in males and females

A
  • Gonadal teratomas in males, all malignant

- Gonadal teratomas in females, most are benign

26
Q

HAMARTOMA

A
  • localised overgrowth of cells and tissues native to the organ.
  • cells are mature but architecturally abnormal
  • common in children, and should stop growing when they do,
  • e.g. bile duct hamartomas, bronchial hamartomas,
  • Look like normal epithelium but the way they are arranged is abnormal -> architectural issue
  • Cytologically normal, architecturally abnormal
27
Q

A benign tumour of glandular tissue is:

  1. An adenoma
  2. A leiomyoma
  3. An adenocarcinoma
  4. A squamous papilloma
  5. A lymphoma
A
  1. An Adenoma
28
Q

A malignant tumour derived from soft tissue is a:

  1. Carcinoma
  2. Sarcoma
  3. Teratoma
  4. Lymphoma
  5. Melanoma
A
  1. Sarcoma
29
Q

What is more important? Stage or Grade?

A

STAGE

30
Q

How do you look at differentiation of tumours?

A

Criteria for assessing differentiation of a malignant tumour:
- Evidence of normal function still present production of:
keratin,
mucin
bile
- Various grading systems - for Ca breast, prostate, colon
- no differentiation, ANAPLASTIC carcinoma,

31
Q

What are anapaestic tumours?

A

So poorly differentiated, you don’t know what it is meant to do etc.

32
Q

TNM

A
  • The grade of a tumour describes its degree of differentiation
  • The stage of a tumour describes how far it has spread
  • Tumours of higher grade (i.e. more poorly differentiated) tend to be of higher stage (i.e. spread further)
  • Overall, stage is more important than grade in determining prognosis
  • The Tumour, Node, Metastasis (TNM) system can be applied, and individualised, to tumour in all sites
33
Q

Grade vs. stage

A
  • Grade looks at: how much of its normal function does it still have?
  • Stage looks at: how far has the tumour spread? How far has it invaded, how big is it?