Neoplasia Flashcards

1
Q

What are the two types of neoplasia

A

Benign and malignant

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2
Q

What features determine how bad a neoplasm is

A

Differentiation
Rate of growth
Local invasion
Metastasis (spread to a distanced site)

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3
Q

Levels of differentiation

A

Well
Moderate
Poor
Anaplastic

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4
Q

Features of poor differentiation

A

Variability in nuclear size/shape
High nuclear:cytoplasm ratio

Increased mitosis activity
Necrosis

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5
Q

Benign tumours

A

Well differentiated
Non invasive
Slow growing
Don’t metastasise
Usually harmless - can be harmful

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6
Q

Malignant tumours

A

Varied differentiation (tends to be poor)
Invasive
Fast growing
Able to metastasise

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7
Q

Dysplasia

A

Neoplastic change or ‘pre-malignancy’
Doesn’t always lead to malignancy/cancer

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8
Q

Metastasis

A

The spread of tumour to another site

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9
Q

How are tumours classified

A

Upon their location

Epithelial/non-epithelial

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10
Q

Types of surface/non-glandular epithelia

A

Squamous
Transitional

offer protection

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11
Q

Types of glandular epithelia

A

Cuboidal
Columnar
Glandular

glands and ducts - secretion

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12
Q

Benign tumour suffix

A

-oma

Exceptions: melanoma, lymphoma, seminoma, mesothelioma

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13
Q

Benign tumour of glandular epithelium suffix

A

Adenoma

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14
Q

Benign tumour of surface epithelium suffix

A

Papilloma

Fingerlike projections

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15
Q

Benign tumour of squamous epithelium (eg. Skin)

A

Squamous cell papilloma

Papilloma - surface epithelium (benign)

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16
Q

Benign tumour of glandular epithelium of the colon

A

Colonic adenoma

Adenoma - glandular epithelium (benign)

17
Q

Benign mesenchymal tumour suffix

18
Q

MESENCHYMAL
A benign tumour of bone is called…
Smooth muscle…
Adipose…
Blood vessel…
Cartilage…
Fibrous tissue…

A

Osteoma
Leiomyoma
Lipoma
Haemangioma
Chondroma
Fibroma

19
Q

Malignant tumours are called…

A

Carcinomas

20
Q

Malignant glandular epithelium tumours are called…

A

Adenocarcinomas

21
Q

Malignant tumour of surface epithelia are called…

A

(cell type) Carcinoma

22
Q

Malignant mesenchymal tumours are called…

23
Q

Precursor cell tumours have the suffix…

A

-blastoma

RetinoBLASTOMA
HepatoBLASTOMA

24
Q

Haematolymphoid malignancies

A

Lymphoma - lymphocytes (B/T)
Myeloma - plasma cells
Leukaemia - WBC (benign in bone marrow)

25
Q

Melanocytic neoplasm

A

Melanoma - melanocytes (produce pigment of skin)

26
Q

Carcinoma in situ

A

Very severe dysplasia

27
Q

Polyploidy

A

When cell contains exact multiples of diploid state

eg. Tetraploidy (4n), octoploidy (8n)

28
Q

Aneuploidy

A

When a cell contains inexact multiples of diploid state

eg. 3n, 7n

29
Q

Function of p53

A
  • Activating DNA repair proteins
  • Stopping cell cycle to allow repair
  • Initiating apoptosis of damaged cells

Made by TP53 - a tumour suppressor gene

30
Q

Angiogenesis

A

Formation of blood vessels

31
Q

What is a tumour suppressor gene

A

Genes which inhibit neoplastic growth

eg. TP53 which encode for p53

32
Q

What is an oncogene

A

Genes which drive the neoplastic behaviour of cells

Produce oncoproteins

Aka- Mutated genes which can cause cancer

33
Q

What is Rb

A

A tumour suppressor gene that codes for retinoblastoma protein

  • Inhibits cell cycle progression until cell is ready to divide (G1 checkpoint)
34
Q

Which tissues are most sensitive to carcinogenic effect of ionising radiation

A

Thyroid
Bone
Breast
Haematopoetic tissue

Skin - UV

35
Q

Routes of metastasis

A

Haematogenous - by blood
Lymphatic - by lymph
Transcoelomic - across a body cavity

36
Q

What is a benign tumour derived from all 3 germ cell layers called

37
Q

The presence of lymph node metastasis mandates less aggressive treatment than does their absence

True/false

A

False

Mandates MORE aggressive treatment

38
Q

What is the sequence of investigations with biopsy specimens in the pathology laboratory

A

Macroscopic examination —> microscopy for cell morphology —> immunohistochemistry —> genetics