Neoplasia Flashcards

1
Q

definitions: Tumour Neoplasia Malignant Benign Cancer Dysplasia

A
  • Tumour - Swelling, now commonly a synonym for ’neoplasm’ - Neoplasia - AUTONOMOUS ‘new growth’ of abnormal cells - Malignant - ‘evil in nature’ / ‘tending to produce death’ - Benign - ‘gentle/kind’ so not harmful or not malignant - Cancer - Synonymous with ‘malignant neoplasm’ - Dysplasia - Autonomous new growth (malignant) that has not yet invaded anything
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2
Q

What are the three ways you classify a neoplasm? future of classification?

A

Behaviour - Benign, borderline, malignant Histogenesis - What’s the cell of origin? Differentiation - Which cells/tissues are seen in the tumour and how well do they resemble normal tissues? molecular classification is likely to become more important than the histogenesis as cells can morph and change

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3
Q

Characteristics of benign neoplasms

A

Remain localised Pushing, well circumscribed borders or encapsulated, no invasion Usually grow slowly Look similar to the parent tissue they have arisen from NO METASTASIS

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4
Q

Problems caused by benign neoplasms

A
  • Pressure effects - Obstruction of hollow organs - Hormone production - Anxiety of the patient - Wide variety of clinical problems - Benign neoplasms may but generally do not transform into malignant neoplasms
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5
Q

define dysplasia

A

Dysplasia describes abnormal cell morphology worrying for a borderline or malignant neoplastic process. Most often seen in epithelial tissues. The cells don’t look normal any more. If dysplasia is seen in an epithelium and the basement membrane remains intact, the neoplasm cannot metastasize and cure is usually possible. This is often called ‘intraepithelial neoplasia’ e.g. CIN, PIN, … or ‘carcinoma in situ’ e.g. DCIS. Dysplasia may (or may not) progress to an invasive neoplasm.

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6
Q

Borderline Neoplasms characteristics

A

Limited invasion but local destructive growth May progress to frank malignancy Often curable Very unlikely to metastasize Examples: Serous borderline tumour of the ovary Basal cell carcinoma

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7
Q

Malignant neoplasms characteristics

A
  • Invasion of surrounding tissues (not localised) - Infiltrative, poorly defined borders - Usually grow relatively rapidly - Variable resemblance to parent tissue METASTASIS
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8
Q

The Hallmarks of Cancer

A
  • Resisting cell death / avoiding apoptosis
  • Deregulating cellular energetics
  • Self sufficiency in proliferative signaling
  • Evading host immune responses
  • Evading growth suppressors
  • Activating invasion and metastasis
  • Two enabling features:
  • Genome instability and mutation,
  • Tumour-promoting inflammation
  • Enabling replicative immortality Induction of angiogenesis
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9
Q

General aetiologies

A
  • Oncogenes
  • DNA / gene mutations
  • Translocations
  • Viruses
  • UV radiation
  • Toxins
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10
Q

What is an oncogene?

A

Oncogene - a gene that has the potential to promote neoplasia

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11
Q

What problems do malignant neoplasms cause?

A
  • Destruction of adjacent tissues
  • Bleeding from ulcers
  • Obstruction of hollow viscera
  • Production of hormones
  • Weight loss
  • Anxiety of the patient
  • Wide variety of clinical problems
  • METASTASIS
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12
Q

What is the difference between grading and staging?

A

Grading describes how well the malignant neoplasm resembles normal tissue

Staging describes the anatomical extend of a malignant neoplasm

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13
Q

Explain Grading

A

Neoplasms vary in the extend to which they resemble normal tissues:

  • The tissue from which they have arisen
  • The tissue towards which they differentiate

The grade of a cancer correlates with prognosis

Examined by microscopic assessment / morphology.

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14
Q

Different classifications of grading:

A

Well differentiated

Moderately differentiated

Severely differentiated

High grade

Low grade

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15
Q

How is staging used in neoplasm

A

Staging reflects the anatomical extend of a cancer

Locally T = tumour

Lymph nodes N = nodes

Metastasis M = metastasis

Different stages will have different prognosis and are amenable to different sorts of treatment

Many different staging systems (individualized to the organ in question)

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16
Q

Classifications now and the future

Histogenesis

Differentiation

future

A

Histogenesis

What’s the cell of origin?

(e.g. Squamous cell carcinoma, melanoma)

Differentiation

Which cells/tissues are seen in the tumour and how well do they resemble normal tissues?

(e.g. Carcinosarcoma)

Future

Classification by molecular and genetic features

Targeted individualised management