Disorders Of Growth And Cancer Flashcards

1
Q

What are cellular adaptations to stress?

A
  • reversible changes in the number/size/type of cells in response to changes in their environment.
  • physiological: responses of cells to normal stimulation by hormones or endogenous chemical mediators
  • pathological: responses to stress that allow cells to modulate their structure/function to avoid/reduce injury
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2
Q

What is hypertrophy and its causes

A
  • increase in size of cells/organ due to increased synthesis of structural proteins and organelles
  • occurs when cells are incapable of dividing
  • causes: increased functional demand, hormonal stimulation
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3
Q

What is hyperplasia and what causes it?

A
  • increase in number of cells in an organ/tissue
  • adaptive response in cells capable of replication
  • physiological: hormonal/compensatory (eg. When a portion of tissue is removed/diseased)
  • pathological: excessive hormonal/growth factor stimulation
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4
Q

What is atrophy and some causes?

A
  • reduction in size/number of cells in organ/tissue due to decreased protein synthesis and increased protein degradation
  • causes: loss of innervation, reduced blood supply, inadequate nutrition, decreased workload, loss of endocrine stimulation, ageing
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5
Q

What is metaplasia with an example?

A
  • reversible change from one fully differentiated cell type into another
  • adatpation that occurs when cells are sensitive to a particular stress and are replaced by cells which are better able to withstand the adverse environment
  • eg. Normal ciliated columnar epithelial cells are replaced by stratified squamous epithelial cells in the respiratory epithelium of smokers
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6
Q

Define neoplasm

A
  • new growth (abnormal)
  • excessive uncoordinated growth compared to adjacent tissues
  • persists even after cessation of causative stimuli
  • usually the result of irreversible genetic change which is passed from one cell to its progeny
  • can be classified according to biological behaviour (benign vs malignant) or tumour type, sub-type and site of origin
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7
Q

Describe features of benign neoplasms

A
  • grows slowly without invading adjacent tissue or spreading to distant sites (localised)
  • usually few cells undergoing cell division which appear normal
  • well circumscribed due to lack of invasion
  • small regular and uniform nuclei
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8
Q

Describe features of malignant neoplasms

A
  • invades surrounding tissues and can spread to distant sites (metastasise) with faster growth rate
  • numerous cells undergoing cell division including atypical cells
  • not well circumscribed
  • larger, pleomorphic nuclei with increased DNA content
  • synonymous with cancer
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9
Q

Contrast benign vs malignant neoplasms in terms of histology, clinically, and treatment

A

Histologically: benign neoplasms resemble the tissue of origin whereas malignant neoplasms can differ from their tissue of origin

Clinically: benign neoplasms cause local effects and hormone secretions, whereas malignant neoplasms can additionally cause destruction, inappropriate hormone secretion and can be fatal

Treatment: benign neoplasms can be treated with local excision, whereas malignant neoplasms may require further therapy with radio/chemo/supportive care

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10
Q

Describe dysplasia

A
  • form of neoplasia which begins as benign but can progress to malignant
  • occurs typically in epithelial cells/melanocytes (surface cells)
  • disordered growth where cells don’t differentiate fully but are contained by a basement membrane (non-invasive)
  • cells appear with larger and darker nuclei
  • can develop from a pre-existing condition or metaplasia
  • can persist, regress or progress
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11
Q

Describe carcinoma in situ

A
  • severe form of dysplasia
  • full-thickness epithelial dysplasia from basement membrane to surface of epithelium (only epithelial neoplasms)
  • if no more advanced than this stage then risk of metastasis is 0 due to lack of blood vessels and lymphatics in epithelium above the basement membrane
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12
Q

How are tumours typed and graded? What is the clinical significance of classifying tumours?

A
  • tumour type = tissue type represented by tumour
  • tumour grade = well differentiated (resembles identifiable tissue type) or undifferentiated (IHC may be needed)
  • important for prognosis and predicted response to treatment
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13
Q

How are epithelial tumours named?

A

Benign = papilloma/adenoma
Malignant = carcinoma/adenocarcinoma

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14
Q

How are connective tissue tumours named?

A

Benign = Oma
Malignant = sarcoma

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15
Q

What are the different modes of cancer spread?

A
  • local invasion (growth into surrounding tissue by direct expansion/invasion)
  • lymphatic spread (common for spread of carcinomas)
  • blood spread (common for sarcomas)
  • transcoelomic (serosal) spread (usually stomach/ovary carcinomas)
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16
Q

What are the local effects of tumours?

A
  • effects of the tumour occupying the space
  • pressure effects (can impair function)
  • locally destructive
  • ulceration and bleeding (anaemia)
  • can induce stromal reaction/fibrosis
  • pain (if nerves invaded)
17
Q

What are the non-metastatic effects of cancers?

A
  • anorexia
  • cachexia
  • malaise
  • anaemia
  • fever (part of systemic inflammatory response and release of inflammatory mediators)
  • paraneoplastic syndromes (due to inappropriate hormone secretion by tumour)
18
Q

Describe TNM staging and further considerations involved in a cancer diagnosis

A
  • tumour (how big? Invasion?), nodes (any involved? How many?), metastases (any spread to distal sites?)
  • any venous/lymphatic invasion?
  • is resection complete?
  • any serosal surfaces involved?