Cancer Week Flashcards

(49 cards)

1
Q

Define hypertrophy, atrophy, hyperplasia, metaplasia, dysplasia, and neoplasia.

A

HT - increase in size. AT - decrease in size/number. HP - increase in number. MP - change in cell type. DP - disordered growth. NP - growth without stimuli

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2
Q

Name the tumour that is benign and non-glandular and non-secretory.

A

Squamous papilloma

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3
Q

Name the type of tumour which is most common.

A

Epithelial (carcinoma)

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4
Q

When a tumour is identified, which type of neoplasia should be assumed until proven otherwise?

A

Carcinoma

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5
Q

What is the name of a tumour affecting the connective, lymphatic, or blood vessel tissue?

A

Sarcomas

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6
Q

Name tumours of smooth and skeletal muscle.

A

Smooth - leiomyosarcoma. Skeletal - rhabdomyosarcoma

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7
Q

Describe spread in sarcomas.

A

Usually only local (not really lymphatic) so can be big

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8
Q

Which type of tumour is most common in children?

A

Sarcoma (carcinomas are very rare in children)

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9
Q

Name the primary brain tumour.

A

Glioma

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10
Q

Why do gliomas not metastasize?

A

Blood-brain barrier

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11
Q

Name the four main categories of cancer treatment.

A

Palliative, radical, adjuvant, neo-adjuvant

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12
Q

What is the difference between neo-adjuvant and adjuvant therapy?

A

Neo-adjuvant therapy is pre-operative to reduce size

Adjuvant therapy is post-operative to reduce recurrence

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13
Q

What are the four endpoints of cancer treatment?

A

Overall-survival, disease free, progression-free, local control

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14
Q

Describe how radiotherapy works and how it is prescribed.

A

Breaks DNA during replication. Prescribed in Grays (Gy) in fractions

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15
Q

Name the chemotherapy agent types.

A

Alkylating agents, platinum salts, anti-metabolites, taxanes, arithrocyclines, topoisomerase inhibitors

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16
Q

Describe the mechanism of the drug herceptin.

A

Blocks HER2 receptors (EGFR)

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17
Q

Name the three main features of genetics in cancer.

A

Autosomal dominant, somatic mosaicism, proliferative/invasive phenotype

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18
Q

Describe the two-hit hypothesis.

A

Both chromosomes (i.e. both mother and father) must be ‘hit’ with a mutation. Therefore one germline mutation increases risk of cancer developing

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19
Q

Name the mechanism and drug inhibiting melanoma.

A

BRAF -> KRAS (verurafenib - BRAF inhibitor)

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20
Q

Name the mechanism and drug inhibiting the Philidelphia chromosome mutation metastasis.

A

ACL (imatinib, Glivec)

21
Q

Name the main treatments of BRCA1/BRCA2.

A

PARP inhibitors, platinum salts, immunotherapy

22
Q

An accumulation of which type of mutation increases risk of breast cancer?

A

SNIP - single nucleotide polymorphisms

23
Q

Describe the markers which indicate high, medium, and low risk of breast cancer in families.

A

High - identified BRCA1 mutation. Medium - young family members with breast/ovary cancer. Low - older members of a family with cancer

24
Q

Name the histological layers of the GI tract.

A

Mucosa (with lamina propria and muscularis mucosa), submucosa, muscularis externa (with inner circular and outer longitudinal layer)

25
What is the difference between serosa and adventitia tissue?
Serosa - outer shiny layer | Adventitia - connects to other tissues
26
What is GALT? How does it appear on histology?
Gut associated lymphoid tissue - purple dots (these are lymphocytes)
27
Describe the TNM classification system.
T1 - breach of muscularis mucosa, T2 - breach of submucosa, T3 - breach of muscularis externa, T4 - escape to other tissues N1 - 1-3 nodes affected, N2 - 4+ affected M1 - distant metastasis identified
28
Name some factors which may increase cancer risk.
Obesity, processed/red meat, alcohol, acrylamide (burned food), smoking, beta-carotene
29
Name some factors which may decrease cancer ris.
Vitamin D, dairy and calcium, physical activity, breastfeeding, coffee
30
Name the biochemical marker which can be used to differentiate the two main prostate conditions.
Prostate specific antigen (PSA) | Benign prostate hypertrophy (BPH) & cancer
31
Describe the role of osteoblasts and osteoclasts.
'blasts lay down bone tissue (using calcium and releasing ASP) and 'clasts break it down.
32
Name the three biochemical markers which may differentiate between bone and liver metastasis.
ALP, GGT, and AFP (for hepatocellular carcinoma)
33
Describe how biochemistry may be used to identify risk of ascites fluid.
Albumin gradient (serum level minus fluid tap level)
34
Define an exudate.
Fluid with a protein of > 30g/L or LDH that is above 2/3 the upper limit of normal (164 units/L)
35
What are the suggestive differences between transudate and exudate?
Exudate - local | Transudate - systemic
36
Describe the role of hypercalcaemia in biochemical cancer assessment.
Ca2+ is high in most cancers. It blocks parathyroid hormone (PTH) so if both are high, malignancy is indicated
37
Name the three main paraneoplastic syndromes associated (in particular) with small cell lung cancer.
Lambert-Eaton, Cushing's, SIADH
38
Name the screening tests for breast and colon cancer.
Mammography and FOB/FIT kits
39
What is the purpose of CT and MRI scans in cancer assessment?
Assesses the relation to multiple sites. IV contrast assesses multiple sites at once
40
What are the four main sites of metastasis?
Brain, bone, liver, lung
41
What is palliative care?
Intends to alleviate symptoms without treating the underlying cause. Improves QoL
42
What are the treatment options for palliative care?
Drug therapy, surgery, drainage, vertebroplasty
43
Describe the pain management model in palliative care.
Non-opioids -> opioids -> somatic fibre interruption
44
Name the five main oncogenes and describe their associated malignancies.
``` ABL -> chronic myeloid leukamia c-MYC -> Burkitt lymphoma n-MYC -> neuroblastoma BCL-2 -> follicular lymphoma RAS -> many cancers, particularly pancreatic ```
45
Name the six main tumour supressors and their associated malignancies.
``` p16 (multiple tumour suppressor) -> melanoma p53 -> many cancers APC -> colorectal cancer BRCA1/2 -> breast/endometrial NF1 -> neurofibramotisis Rb -> Retinoblastoma ```
46
Which oncogene is associated with Burkitt lymphoma?
c-myc
47
Which oncogene is associated with follicular lymphoma?
BCL-2
48
Which tumour suppressor is associated with colorectal cancer?
APC
49
Which tumour suppressor is associated with chronic myeloid leukemia?
ABL