2.15 - Cancer Flashcards

1
Q

What is a tumour?

A
  • any kind of mass forming lesion
  • may be neoplastic or non-neoplastic (hamartomas, inflammatory e.g. nasal polyps and heterotopias)
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2
Q

What is a neoplasm?

A
  • the autonomous growth of tissue which have escaped normal constraints on cell proliferation
  • autonomous means they don’t require external stimuli and grow on their own
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3
Q

What are the two types of neoplasms?

A
  • benign (remain localised) or malignant (invade locally and/or spread to distant sites - metastasis)
  • cancers are malignant neoplasms
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4
Q

What do benign neoplasms look like?

A
  • well differentiated and look like normal tissue - neoplasm is sharply demarcated from surrounding tissue
  • cannot tell the difference between benign neoplasm and surrounding tissue
  • fibroadenomas in young women are benign neoplasms that are mobile (can move them around as they aren’t stuck to the skin or the underlying pectoralis muscles)
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5
Q

What do malignant neoplasms look like?

A
  • irregular margins
  • fixed to muscle/skin which shows that it is invasive as it is invading locally
  • e.g. malignant neoplasm in breast, grows into the fat
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6
Q

What is important to note about deaths caused by malignant vs benign tumours?

A
  • many malignant tumours rarely cause death (especially skin cancers - invade locally but low chance of metastasising) and some benign tumours do kill (due to their location e.g. brain)
  • malignant skin cancer is very common and invades locally but has low chance of metastasising so can be controlled easily
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7
Q

What are hamartomas?

A
  • localised benign overgrowths of one or more mature cell types e.g. in the lung
  • they represent architectural but not cytological abnormalities
  • e.g. lung hamartomas are composed of cartilage and bronchial tissue - there is nothing special about the tissue itself but in the way they are arranged –> would cause a lump on an X-ray
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8
Q

What are heterotopias?

A
  • normal tissue being found in parts of the body where they are not normally present
  • e.g. bits of pancreas in the wall of the large intestine (whereas it should be in the retroperitoneum)
  • if we look endoscopically into stomach we can see a lump but if we look under a microscope we can tell it is just a heterotopic pancreas
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9
Q

What is the primary and secondary descriptions of neoplasms based on?

A
  • primary - the cell origin
  • secondary - whether it is benign or malignant
    E.g. tumours of the cartilage are described as:
  • chondromas (benign) or chondrosarcomas (malignant)
  • chondro means cartilage
  • oma means benign and sarcoma means malignant (soft tissue) tumour
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10
Q

Epithelial neoplasms

A
  • type of epithelium - benign tumour - malignant tumour - examples
  • squamous - squamous papilloma - squamous cell carcinoma - skin, oesophagus, cervix
  • glandular - adenoma - adenocarcinoma - breast, colon, pancreas, thyroid
  • transition (can deal with changes in volume) - transitional papilloma - transitional cell carcinoma - bladder
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11
Q

Connective tissue neoplasms

A
  • type of connective tissue - benign tumour - malignant tumour - examples
  • smooth muscle - leiomyoma - leiomyosarcoma - uterus, colon
  • bone - osteoma - osteosarcoma (osteogenic sarcoma) - arm, leg
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12
Q

Haematological neoplasms

A
  • haematological neoplasms - benign tumour - malignant tumour - examples
  • lymphocytes - extremely uncommon - lymphoma (based in lymph nodes) - gastric lymphoma
  • bone marrow - extremely uncommon - leukaemia - acute lymphoblastic leukaemia, chronic myeloid leukaemia
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13
Q

What are teratomas?

A
  • tumours derived from germ cells and can contain tissue derived from all three germ layers (ectoderm, mesoderm, endoderm)
  • they may contain mature/immature tissues and even cancers
  • will be in male/female reproductive tract because of germ cell involvement
  • benign teratomas contain hair and are lined by skin - these are normal adult tissues, just in the ovary where they shouldn’t be = mature teratoma
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14
Q

What malignant tumours are there that end in ‘oma’?

A
  • (malignant) lymphoma
  • (malignant) melanoma
  • hepatoma (liver cell cancer)
  • teratoma (can contain mature/immature elements or carcinoma, not all are malignant)
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15
Q

What are the differences between benign and malignant tumours?

A
  • invasion
  • metastasis
  • differentiation
  • growth pattern
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16
Q

What is invasion?

A
  • direct extension into the adjacent connective tissue and/or other structures e.g. blood vessels
  • this is what distinguishes dysplasia/carcinoma in situ from cancer - dysplasia is non-invasive
  • carcinoma in situ is the most severe degree of dysplasia but still in situ (in its place) so not invaded other tissues, so not cancer
  • e.g. invasive squamous cancer - non-invasive part is dysplastic squamous epithelium, invasive part has evoked a lymphoid response and is cancerous
17
Q

What is metastasis?

A
  • spread via blood vessels etc to other parts of the body
  • all malignant tumours have the capacity to metastasise although they may be diagnosed before they have done so
  • metastasis makes it harder to treat cancer than if it stays in one local area - need chemotherapy and prognosis is worse
18
Q

What is differentiation?

A
  • how much the cells of the tumour resemble the cells of the tissue it is derived from
  • tumour cells tend to have larger nuclei (and hence higher nuclear-cytoplasmic ratio) and more mitoses than normal tissue they’re derived from
  • they may have abnormal mitoses (e.g. tripolar) and marked nuclear pleomorphism (variability in nuclear size and shape)
19
Q

What are the differences between cancerous looking cells and normal cells?

A
  • large, variably shaped nuclei
  • many dividing cells
  • disorganised arrangement
  • variation in size and shape
  • loss of normal features
20
Q

What is the growth pattern?

A
  • how much does the architecture of the tumour resemble the architecture of the tissue it is derived from
  • tumours have less well-defined architecture than the tissue they are derived from
  • the less well-differentiated a tumour is, the worse the architecture will get
21
Q

What is the progression of a cancer like? e.g. colonic tumour

A
  • starts off as adenoma - benign tumour of glandular epithelium - hyperproliferation –> adenomatous polyps
  • then severe dysplasia occurs (not cancer yet as it is still confined to mucosa) - pre cancerous polyp
  • then it becomes an adenocarcinoma as the tumour invades the underlying tissue
  • then finally the tumour grows more all the way through the wall = invasive cancer
22
Q

By which routes do tumours spread?

A
  • direct extension
  • haematogenous
  • lymphatic
  • transcoelomic
  • perineural
23
Q

What is direct extension?

A
  • associated with a stromal (connective tissue) response to the tumour
  • includes fibroblastic proliferation (a demoplastic response), vascular proliferation (angiogenesis) and an immune response
24
Q

What is the haematogenous route?

A
  • via blood vessels - usually venules and capillaries due to thinner walls
  • most sarcomas metastasise first via blood vessels
  • vascular invasion: e.g. if left blood vessel has RBCs but right one doesn’t, and has tumour instead
25
Q

What is the lymphatic route?

A
  • via lymphatics to lymph nodes and beyond
  • the pattern of spread is dictated by the normal lymphatic drainage of the organ in question
  • most epithelial cancers metastasise first via the lymphatics
  • e.g. carcinomas in lateral aspect of breast will go to lymph nodes in axilla because that is the lymphatic drainage point
26
Q

What is the transcoelomic route?

A
  • via seeding of body cavities
  • commonest examples are the pleural cavities (for intrathoracic cancers e.g. lung) and peritoneal cavities (for intra-abdominal cancers e.g. GI tract, stomach)
  • peritoneal cavity is low resistance zone, moist and constantly moving = facilitates tumour spread
27
Q

What is the perineural route?

A
  • via nerves
  • underappreciated route of cancer spread
  • good way for tumours to spread as low resistance pathway and for some cancers like liver ones, it is common to spread this way
28
Q

How do we assess tumour spread?

A
  • clinically - examining patient e.g. examining lymph nodes of patient / lump on breast
  • radiologically - CT scans, planning X-ray
  • pathologically - definitive means of staging tumours (how far they have spread)
28
Q

How do we describe tumour spread (stage)?

A
  • T = tumour - tumour size or extent of local invasion
  • N = nodes - number of lymph nodes involved
  • M = metastases - presence of distant metastases
  • this is the TNM system and the details are different for each type of tumour
  • dictate patient prognosis and treatment
29
Q

What is the meaning of grade and stage?

A
  • grade - how differentiated is the tumour?
  • stage - how far has the tumour spread?
  • the worse the grade/stage, the worse the prognosis
  • in terms of tumour prognosis, stage is more important than grade
  • if tumours are high grade, they tend to be high stage - main prognostic factor