13 Neoplasia 1 Flashcards

1
Q

Define ‘Neoplasm’.

A

Abnomal growth of cells- persists after initial stimulus removed

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2
Q

Define ‘Malignant Neoplasm’.

A

(Abnomal growth of cells- persists after initial stimulus removed) + invades surrounding tissue w./ potential spread to distant sites

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3
Q

Define ‘Tumour’.

A

Clinically detectable lump/ swelling.

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4
Q

Define ‘cancer’

A

Malignant neoplasm

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5
Q

Define ‘metastasis’

A

Malignant neoplasm- spreads from original site to new non-contiguous site (secondary site)

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6
Q

What is ‘dysplasia’?

A

Pre-neoplastic alteration- cells= disordered

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7
Q

How is dysplasia different from neoplasia?

A

Dysplasia=reversible, neoplasia isn’t

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8
Q

What’s the difference between benign and malignant neoplasms?

A

Benign- remain confined to site of origin don’t produce matastases Malignant- have potential to metastasise

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9
Q

How do benign and malignant neoplasms appear different to the naked eye?

A

Benign- grow- confined area- pushing outer margin (pseudo capsule) Malignant- irregular outer margin, shape + potential areas of necrosis/ ulceration

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10
Q

How do benign and malignant neoplasms appear different under the microscope?

A

Benign= well differentiated (resemble parent tissue) Malignant= range- poorly–> well differentiated

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11
Q

What are anaplastic cells?

A

Cells- no resemblance to any tissue

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12
Q

How do cells with WORSENING differentiation appear under the microscope?

A

-Increased nuclear size to cytoplasmic ratio -Increased nuclear staining (hyperchromasia) -More mitotic figures -Increased variation- size and shape of cells and nuclei (pleomorphism)

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13
Q

If a neoplasm is labelled as ‘high grade’ by a clinician, what does this mean?

A

It is poorly differentiated

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14
Q

What causes neoplasia?

A

Mutations caused by: -initiators (mutagenic agents) - e.g. chemicals/infections -promoters (cell proliferation) (mutations can be inherited/external) –>cause expanded, monoclonal (originating from same cell) population of mutant cells then: PROGRESSION- accumulation of more mutations

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15
Q

What is ‘lyonisation’?

A

Random inactivation of 1 allele in early female embryogenesis

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16
Q

What are proto-oncogenes?

A

Genes coding for proteins responsible for cell proliferation

17
Q

What are tumour suppressor genes?

A

Protect cell from becoming cancerous- slow cell division, correct mistakes etc.

18
Q

What is an oncogene?

A

When proto-oncogene= abnormally activated (favour neoplasm formation)

19
Q

What do the names of all BENIGN neoplasms end in?

A

-oma

20
Q

What do the names of MALIGNANT EPITHELIAL neoplasms end in?

A

-carcinoma

21
Q

What do the names of MALIGNANT STROMAL neoplasms end in?

A

(stromal= CT cells) -sarcoma

22
Q

What is a carcinoma called if it has not invaded through the basement membrane?

A

in-situ

23
Q

What is a carcinoma called if it has penetrated through the basement membrane?

A

invasive

24
Q

What is the name of.a malignant neoplasm of blood forming cells arising in bone marrow?

A

Leukaemia

25
Q

What is the name for a malignant neoplasm of the lymphocytes- mainly affecting lymph nodes?

A

Lymphomas

26
Q

What is the name of a malignant neoplasm affecting plasma cells?

A

Myeloma

27
Q

From what type of cell do germ cell neoplasms arise from?

A

Pluripotent cell (Testis/ovary)

28
Q

What are ‘-blastomas’?

A

Neoplasms formed from immature precursor cells (mainly in children)