tumour pathology Flashcards

1
Q

definition of a tumour

A

abnormal growing mass of tissue:

uncoordinated growth

growth continues after removal of growth stimulus

irreversible change

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2
Q

epithelial tumours: name for benign glandular tumour

A

adenoma

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3
Q

epithelial tumours: name for malignant glandular tumour

A

adenocarcinoma

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4
Q

epithelial tumours: name for benign squamous tumour

A

squamous papilloma

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5
Q

epithelial tumours: name for malignant squamous tumour

A

squamous carcinoma

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6
Q

tissue tumours: name for benign bone tumour

A

osteoma

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7
Q

tissue tumours: name for malignant bone tumours

A

osteosarcoma

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8
Q

tissue tumours: name for benign fat tumour

A

lipoma

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9
Q

tissue tumours: name for malignant fat tumour

A

lipo-sarcoma

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10
Q

tissue tumours: name for benign fibrous tumour

A

fibroma

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11
Q

tissue tumours: name of malignant fibrous tumours

A

fibrosarcoma

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12
Q

name for malignant WBC tumour

A

leukaemia

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13
Q

name for malignant lymphoid tumour

A

lymphoma

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14
Q

name for benign melanocyte tumour

A

naevus

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15
Q

name for malignant melanocyte tumour

A

melanoma

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16
Q

CNS tumour

A

astrocytoma

17
Q

PNS tumour

A

schwannoma

18
Q

germ cell tumours

A

teratomas

ovarian usually benign

testicular usually malignant

19
Q

benign tumour features

A

encapsulated

cells similar to normal

well differentiated

similar function to normal tissue

20
Q

local effects of benign tumours

A

pressure

obstruction

21
Q

local effects of malignant tumours

A

pressure and obstruction

destruction- ulceration and infection

bleeding

pain

22
Q

systemic effects of malignant tumours

A

weight loss- cachexia

secretion of hormones

paraneoplastic syndrome

23
Q

what’s the earliest stage in process of malignancy that can be visualised

A

dysplasia

24
Q

where is dysplasia found

A

epithelium- no invasion

25
Q

features of dysplasia

A

disorganisation of cells

no invasion

high or low grade

26
Q

phases of cell cycle

A

M- mitosis

G1- prep for DNA synthesis

S- DNA synthesis

G2- prep for mitosis

G0- quiescence

27
Q

the G1- S checkpoint checks for

A

nutrients and DNA damage

28
Q

the S- G2 checkpoint checks for

A

unreplicated or damaged DNA

29
Q

the G2- M checkpoint checks for

A

unreplicated or damaged DNA

30
Q

the M- G1 checkpoint checks for

A

chromosome musalignment

31
Q

cell cycle checkpoint activators

A

CDK’s activated by cyclin

32
Q

what do active CDK/cyclin complex’s do

A

phosphorylation of target proteins

33
Q

CDK inhibitors

A

INK4A gene family- p16

CIP/KIP gene family- p21, p27

34
Q

2 main regulator pathways that get disrupted in cancer

A

D-pRb-E2F- retinoblastoma tumour suppressor

p53 pathway- apoptosis

35
Q

cells with mutated p53 don’t

A

G1 arrest or repair damaged DNA

36
Q

2 hit hypothesis of anti oncogenes

A

tumour suppressor alleles are usually recessive- needs both normal alleles to be missing to cause cancer

37
Q

what are proto-oncogenes and oncogenes

A

proto-onco: normal genes that code growth regulating proteins

oncogenes: mutated proto oncogenes with gain of function

38
Q

benign tumours that show abnormalities and risk spreading are known as

A

dysplastic