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Flashcards

Week 8

Dolu Falowo Foundations 4 Inglês 39 flashcards

Flashcards do conjunto (39)

  1. 1Define benign-Localised lesion
    -Can affect surrounding tissues by mass effect
    -Doesn't metastasise
  2. 2Define malignant-Aggressive behaviour
    -Invade local tissue
  3. 3What are the 2 basic components of tumours?-Parenchyma
    -Supporting stroma (connective tissue and blood vessels)
  4. 4Examples of benign mesenchymal tumours-Fibroma
    -Osteoma
    -Leiomyoma
    -Angioma
  5. 5Examples of benign epithelial tumours-Adenoma
    -Cystadenoma
    -Papilloma
    -Polyp
  6. 6Define mixed tumoursDerived from a single germ cell layer that differentiates into more than 1 cell type
  7. 7Define teratomasDerived from more germ cell layers and so it composed of many parenchymal cell types
  8. 8What are the characteristics of of neoplastic cells?-Pleomorphism
    -Abnormal nuclear morphology
    -Abundant atypical mitosis
    -Loss of polarity
    -Tumour giant cell
    -Ischaemic necrosis
  9. 9Define dysplasia-Loss of cellular uniformity and organisation
    -Once the inciting stimulus is removed, it reverts back to its normal state
  10. 10What determines the rate of growth?-Excess cell production over cell loss
    -Growth fraction (% of actively proliferating cells in a tumour)
    -Inversely correlated with the level of differentiation
  11. 11Describe what a benign tumour would look like-Expansile mass
    -Ring of condensed capsule surrounds the tumour
    -Tumour does not penetrate the capsule
    -Can be enucleated surgically
  12. 12Describe what a malignant tumour would look like-Invasive and infiltrates surrounding tissue
    -Lacks well-defined capsule
    -Surgery requires mass to be removed with a healthy margin
  13. 13What are the 3 main mechanisms of cancer spread?-Direct extension/local spread
    -Lymphatic spread
    -Haematogenous spread via venous system
  14. 14How does direct extension/local spread work?-Tumour extends directly into surrounding tissue, organs, spaces
    -Occurs through the wall of the primary organ
    -Seeding can occur in the peritoneal/pleural cavity where detached cells enter the fluid
  15. 15What are the common primaries of cancers which spread in the peritoneum?Intraperitoneal organs
    -oesophageal
    -gastric
    -colorectal
    -pancreatic
    -ovarian
  16. 16Where does peritoneal spread occur to?-Peritoneal surfaces of organs eg. liver
    -Can plant on omentum (omental cake)
    -Transcoelomic spread can occur (spread into cavities)
  17. 17What is the cisterna chyli?Receives lymph from lower limbs, lumbar trunks and intestinal trunk
  18. 18Describe lymphatic spread of cancer-Cell detach
    -Enter lymph capillaries draining adjacent tissues (no functional capillaries in tumour)
    -Colonise distant tissues
  19. 19What is the sentinel lymph node(s)?-First lymph node/group of lymph nodes that drain a tumour
  20. 20What are sentinel lymph nodes used for?-Predicting the likelihood of metastases (staging)
    -Identified via methylene blue or a radioactive tracer and biopsied
    -Used in staging for breast, colon cancer and melanoma
  21. 21How does haematogenous spread of cancer occur?-Cells detach
    -Enter venous vessels draining the tissue
    -Commonly metastasise to liver, lung, brain and bone
  22. 22How does haematogenous spread of the liver occur?-From structures drained by the portal venous system eg. GI tumours
    -Venous drainage of the liver is via the mesenteric veins and hepatic portal system
  23. 23How does haematogenous spread of the lungs occur?-From structures drained by the systemic venous system (harder to determine)
    -Cells enter the right circulation via the SVS/IVC into the RHS of the heart and pulmonary system
  24. 24What are examples of cancers that commonly metastasise to the bone?-Breast
    -Lung
    -Thyroid
    -Kidney
    -Prostate
  25. 25Define screening-Investigation of asymptomatic people in order to classify them as likely or unlikely to have the disease
    -Those who appear likely to have the disease, undergo further testing before a diagnosis is made
  26. 26What are the essential prerequisites for screening (WHO)? (10)-Condition is an important public health problem
    -Accepted treatment is present
    -Facilities to do so should be present
    -Recognised presymptomatic/latent phase
    -Suitable test or examination
    -Test should be acceptable
    -Natural history of disease should be understood
    -Agreed policy on treatment
    -Economically balanced
    -Case funding should be continuous
  27. 27Characteristics of diseases suitable for screening-Relatively common and have severe consequences
    -Must have a preclinical phase where it is undiagnosed but detectable
    -Early treatment must offer some advantage
    -Evidence of net benefit
  28. 28Describe lead time bias-The day diagnosis is made is brought forward by screening
    -There is an apparent increase in survival since the period between detection and death is longer than in those not screened
  29. 29Describe length bias-Diseases which are screened, are more likely to be less aggressive
    -Less aggressive conditions are more likely to be present for years
    -More aggressive conditions are likely to develop fully between successive routine screening points
  30. 30Define sensitivityProportion with condition who test positive
    true positive/total disease present
  31. 31Define specificityProportion without the condition who test negative
    true negative/disease absent
  32. 32Define positive predictive valueProportion with positive test who have the condition
    true positive/positive screening result
  33. 33Define negative predictive valueProportion with negative test who do not have the condition
    true negative/negative screening result
  34. 34D-Free screening for women aged 50-70 every 3 years
    -Ductal carcinoma in-situ numbers have risen since it is not palpable (only detectable on mammograms)
  35. 35What are the problems with PSA testing?-2/3 of men with elevated levels do not have prostate cancer
    -Test is unreliable between different labs
    -Natural history of the disease is poorly understood
    -Substantial proportion receive unnecessary treatment with serious s/e's
  36. 36What are the objectives of cancer treatments?-Cure the patient
    -Prolong patient survival
    -Palliate symptoms
  37. 37What is the purpose of phase 1 RCTs?To find a safe dose of a new treatment and understand toxicities. Determines dose and toxicities.
  38. 38What is the purpose of phase 2 RCTs?To determine if new treatment has sufficient efficacy to be worthy of further investigation. Determines anti-disease activity.
  39. 39What is the purpose of phase 3 RCTs?To provide sufficient evidence to potentially change clinical practice. Determines long-term efficacy measure.

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Descrição
Anatomy and cancer Cancer screening and prevention How do you know that a treatment works?
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Dolu Falowo
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