Principles Flashcards

1
Q

What is the definition of metaplasia?

A

A REVERSIBLE change in which one adult cell type (usually epithelial) is replaced by another adult cell type – can be physiological or pathological.

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2
Q

Examples of physiological, adaptive metaplasia? (x2)

A

Columnar epithelium of cervix changes to squamous when exposed to more acidic environments. Similarly, oesophagus – in acid reflux, changes from squamous to columnar – Barrett’s oesophagus.

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3
Q

What is the definition of dysplasia?

A

Abnormal pattern of growth where some of the cellular and architectural features of malignancy are present – INTACT BASEMENT MEMBRANE, hence non-invasive.

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4
Q

What are the features that describe dysplasia? (x4)

A

 Loss of architectural orientation.  Loss of uniformity of individual cells.  Nucleus:cytoplasm ratio is enlarged – nuclei become hyperchromatic, so looks histologically DARKER.  Mitotic figures – abundant, abnormal and in places not usually expected.

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5
Q

Where is dysplasia common? (x6)

A

• CERVIX – HPV infection. • BRONCHUS – Smoking. • COLON – Ulcerative colitis. • LARYNX – smoking. • STOMACH – pernicious anaemia. • OESOPHAGUS – acid reflux.

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6
Q

What are the two dysplasia classifications? Difference?

A
  • LOW GRADE: low risk of progression and likely to be easily reversible.
  • HIGH GRADE: likely to progress and less likely to spontaneously regress.
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7
Q

Relationship between metaplasia and dysplasia?

A

Metaplasia and dysplasia tend to occur together - and explain how can get cancers of wrong type of epithelium e.g. Squamous lung cell cancer.

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8
Q

What is neoplasia? Other names? (x2)

A

aka TUMOUR or MALIGNANCY. Describes an abnormal, autonomous proliferation of cells unresponsive to normal growth control mechanisms.

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9
Q

What are the differences between a malignant and benign tumour? (x6)

A

Look at photo.

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10
Q

In what circumstances may benign tumours be fatal? (x6)

A

• If there are in a dangerous place e.g. meninges or pituitary. • The tumour secretes something dangerous e.g. insulinoma. • Gets infected e.g. bladder. • Bleeds e.g. GI tract. • Ruptures e.g. liver adenoma. • Torts (twisted) e.g. ovarian cysts.

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11
Q

What is a metastasis? What factors determine this?

A

A discontinuous growing colony of tumour cells, at some distance from the primary cancer i.e. spread. These depend on the lymphatic and vascular drainage of the site of the primary tumour.

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12
Q

What is the nomenclature of benign epithelial tumours?

A

• PAPILLOMA: of the surface epithelium e.g. skin or bladder. • ADENOMA: of glandular epithelium e.g. stomach, thyroid, colon, kidney, pituitary, pancreas.

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13
Q

What is a carcinoma?

A

A malignant tumour derived from EPITHELIUM e.g. squamous cell carcinoma, adenocarcinoma, transitional cell carcinoma, basal cell carcinoma.

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14
Q

What is a benign soft tissue tumour?

A

Benign tumours of soft tissue. Soft tissue is of mesodermal origin – including, muscle, tendons, ligaments, fascia, fat. They are all connective tissues.

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15
Q

What is a sarcoma?

A

A malignant tumour derived from cells of mesenchymal origin – SOFT TISSUE, describing connective tissue cells. Sarcomas also include bones, although these are not ‘soft’.

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16
Q

What is the nomenclature of sarcomas? (x6)

A

• Liposarcoma – fat. • Osteosarcoma – bone. • Chondrosarcoma – cartilage. • Rhabdomyosarcoma – striated muscle. • Leiomyosarcoma – smooth muscle. • Malignant Peripheral Nerve Sheath Tumour – nerve sheath.

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17
Q

What is the difference between leukaemia and lymphoma?

A

• They are both cancers of the blood. • LEUKAEMIA: malignant tumour of bone marrow derived cells in circulating blood. • LYMPHOMA: malignant tumour of lymphocytes in lymph nodes.

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18
Q

What is teratoma? Sex difference?

A

Tumour derived from germ cells which have the potential to develop to tumours of all three germ cell layers – ectoderm, mesoderm AND endoderm. In males, all gonadal teratomas are MALIGNANT; in females, most gonadal teratomas are BENIGN.

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19
Q

What is hamartoma?

A

Localised overgrowth of cells/tissues native to the organ – cells are mature but architecturally abnormal. In other words, the cells look completely normal, but they way they’re arranged is abnormal.

20
Q

How is differentiation of a tumour assessed? (x2) No differentiation in tumour?

A

• Look for evidence of normal function e.g. secreting what it should be secreting. • Employ a GRADING SYSTEM. • If a tumour has NO differentiation, it is an ANAPLASTIC carcinoma.

21
Q

What is the ‘grade’ and ‘stage’ of a tumour?

A

GRADE describes degree of differentiation; STAGE describes how far it has spread.

22
Q

Out of stage and grade, which is more important?

A

Stage is more important in determining prognosis.

23
Q

How are tumours staged?

A

• TNM system – tumour, node, metastasis. • TUMOUR: TX (not assessed), and then T0-T4 based on invasion. • NODES: NX (not assessed), and then NO-N3 based on number and size of nodes. • METASTASIS: M0-M1 (not spread/spread). • Changes for each organ regularly.

24
Q

What is a carcinogen?

A

Substance which promotes the formation of cancer.

25
Q

What are the 10 ‘hallmarks’ of the cancer cell? !!!

A

• Self-sufficient (survives with minimal stimulation). • Insensitive to anti-growth signals (grows regardless of intake). • Anti-apoptotic. • Pro-invasive and metastatic. • Pro-angiogenic (recruits blood vessels –> keeps cancer well-vascularised). • Non-senescent (does not deteriorate with age). • Dysregulated metabolism. • Evades the immune system. • Genome instability and mutation. • Promotes inflammation.

26
Q

What are the most common cancer deaths in men in the UK? Compared to the world?

A

UK: Lung, prostate, colorectum, oesophagus and pancreas. WORLD: lung, liver, stomach, colorectum and oesophagus.

27
Q

What are the most common cancer deaths in women in the UK? Compared to the world?

A

UK: lung, breast, colorectum, ovary and pancreas. WORLD: breast, lung, colorectum, cervix and stomach.

28
Q

What has happened to trends in cardiovascular deaths compared to cancer deaths in the Western world?

A

Mortality from heart diseases have been declining, whereas cancer deaths have remained stable.

29
Q

What countries have the highest incidence of cancer? Why may this be? (x2) !

A

Incidence is concentrated in the west. Suggestions include because more people are screened in the west, and our unhealthy lifestyles (including alcohol intake and obesity).

30
Q

What do migrant studies show (irrelevant of cancer), if there is (i) a rapid change in risk of disease incidence, (ii) slow change in risk of disease incidence, and (iii) no change in risk of disease incidence following migration?

A
  1. RAPID CHANGE in risk of disease incidence following migration implies that lifestyle/environment factors are more responsible for disease development. 2. SLOW CHANGE in risk of disease incidence following migration implies that exposures in early life are most relevant. 3. PERSISTANCE of risk of disease incidence suggests that genetics are responsible for determining risk.
31
Q

What has happened to trends in incidence of common cancers?

A

Has increased in both men and women in high- (with some cancer incident rates plateauing) and low-income countries. However, it is important to note that incidence has fallen in cancers caused by infectious disease e.g. cervical cancer (though this is only in high-income countries).

32
Q

What are possible explanations for the trends in incidence of cancer across the world? (x2)

A

Changes to exposure in risk factors e.g. diet, AND more comprehensive screening and diagnostic programmes allowing for greater detection of cancers.

33
Q

What has happened to trends in mortality of common cancers?

A

Mortality is decreasing in high-income countries, but not in low-income countries.

34
Q

What are possible explanations for the declining mortality rates of cancers in high-income countries?

A

More effective therapies AND earlier detection of cancers.

35
Q

What is the difference between incidence and prevalence?

A

Incidence is the number of newly diagnosed patients, whereas prevalence refers to the total number of patients within a population.

36
Q

What has happened to prevalence of cancer worldwide? Possible explanations for this? (x3)

A

INCREASED due to demographic countries (ageing populations and increasing size), Westernization of lifestyles (leading to changes in risk factor exposures and subsequent increase in incidence), and people surviving longer with cancer due to more effective management of the disease.

37
Q

What will happen to incidence of certain types of cancers as countries transition from low- to middle- or high-income countries? (x2)

A

Proportion of cancers due to infection decrease such as cervical and stomach, and ‘western’ cancers increase such as lung and colon cancer.

38
Q

What proportion of cancers are from inherited conditions that INCREASE RISK of cancer?

A

5-10% of cases e.g. xeroderma pigmentosum, Paget’s disease of bone and Familial adenomatous polyposis.

39
Q

What are the main risk factors of cancer? What are the values for their attributable risk? (x6)

A
  1. Smoking – 30%. 2. Diet – 20-50%. 3. Infection – 15%. 4. Alcohol – 5%. 5. Occupation – 3%. 6. Reproductive hormones – 15%.
40
Q

What is attributable risk?

A

Difference in risk between the incidence rates in exposed and non-exposed populations.

41
Q

What is the estimate of the impact of changing exposure to risk factors on the risk of developing preventable cancers?

A

45% of cancer in men, and 40% in women could be prevented, had risk factors been reduced to the optimal level, or eliminated (like smoking). Reduction of the same risk factors would also lead to a substantial reduction in the cases of CVD, renal disease, hepatic disease and diabetes (2012 estimate).

42
Q

What is the effect of smoking on cancer? (x2 points)

A

Smoking accounts for at least 30% of all cancer deaths, and causes 90% and 80% of lung cancer deaths in men and women respectively.

43
Q

What is the effect of alcohol on cancer? (x2 points)

A

All types of alcohol can lead to cancer in pharynx, larynx, oesophagus and liver, although mechanisms are poorly understood. Alcohol synergises with smoking.

44
Q

What is the effect of BMI on cancer? Why?

A

Obesity is associated with increased relative risk of post-menopausal breast cancer, colon, pancreatic and endometrial cancer. This is because obesity is an inflammatory disease, resulting in chronic inflammation – a hallmark of cancer.

45
Q

What is the effect of reproductive hormones on cancer?

A

Postmenopausal sex steroids lead to increased relative risk of breast cancer.

46
Q

What is defined as the ‘Western lifestyle’? Consequences?

A

• Energy dense diet, rich in fat, refined carbohydrates and animal protein. • Low physical activity. • Smoking and drinking. • Consequences: greater adult body height, early menarche (menstruation), obesity, diabetes, CVD and hypertension.

47
Q

List examples of infectious agents and the cancer they increase risk of? (x4)

A

• HPV – Cervix, Head and neck. • EBV – Hodgkin’s lymphoma and Burkitts. • HCV and HBV – liver. • H. Pylori – stomach.