ONCO Flashcards

1
Q

name the 5 most common site for head and neck cancers

A

nasophrynx
oral cavithy
oropharynx
hypopharynx
larynx

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2
Q

what is the most commonhistological type of head & neck cancer

A

squamous ce3ll carcinoma

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3
Q

what is the main risk factor for Head and neck cancers

give 2 others

A

HPV (16)

2 others: alcohol, smoking, EBV

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4
Q

give 5 Sx suggesting head & neck cancer

A
  • Dysphagia
  • odynophagia
  • dysphonia ,
  • ALARM symptoms ( tiredness, unexplained weight loss, loss of appetite)
  • Lymphadenopathy
    o Many cancers may just present as a neck lump due to metastasis to lymph node
  • airway compromise (stridor)
  • halitosis
  • focal neurology (VII cranial nerve palsy)
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5
Q

what is the genetic inheritance of Li-Fraumeni syndrome

A

Autosomal dominant

an inherited condition that is characterized by an increased risk for certain types of cancer (sarcomas/ leukaemiaS)

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6
Q

mutations to what gene causes Li-Fraumeni syndrome

A

p53 tumour suppressor gene

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7
Q

what cancers are associated with Li Fraumnei syndrome

A

an inherited condition that is characterized by an increased risk for certain types of cancer.

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8
Q

when are Ix for Li-Fraumeni syndrom conducted

A

Hx sarcoma in <45 yo

1st degree relative with cancer <45 + other family member with malignancy (<45yo) or sarcoma ( any age)

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9
Q

on what chromosome is BRCA 1 carried

A

17

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10
Q

what chromosome is the BRCA 2 gene found

A

13

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11
Q

the BRCA genes are associated with a 60% risk of developing breast cancer. what other cancer are females with these genes at risk of devloping

A

ovarian
( 55% risk with BRCA 1 , 25% risk with BRCA 2)

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12
Q

the BRCA genes are associated with a 60% risk of developing breast cancer. Which of these genes increases the risk of what other cancer in males ?

A

prostate
BRCA 2

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13
Q

what is hereditary non-polyposis colorectal cancer (HNPCC) also known as

A

lynch syndrome

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14
Q

what is the hereditary pattern of lynch syndrom

A

AD

( as with Li-Fraumeni)

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15
Q

what cancers are people with Lynch syndrome at risk of devloping at a young age?

A

colonic
endometrial

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16
Q

what criteria is used to determine the risk of having lynch syndrome

A

amsterdam criteria

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17
Q

what are the features of amsterdam criteria

A

> /=3 family members with confirmed colorectal cancer ( 1 is 1st degree relative of the other 2)
2 successive affected generations
/= 1 colon cancer in diagnosed <50yrs
Familial adenomatous polyposis has been excluded

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18
Q

what gene is mutated in Gardners syndrome

A

APC gene (chromosome 5)

19
Q

what is the genetic inheritance of gardners syndrome

A

AD
( like Li-Fraumeni (breast cancer) and Lynch (colon cancer) )

20
Q

what are the non-GI signs of gardners syndrome

A

skull osteoma, thyroid cancer and epidermoid cysts, dental issues (e.g caries/ supernumary teeth)

21
Q

what Mx is often used in pts with Gardners syndrome

A

colectomy to reduce colorectal cancer risk

22
Q

what anti-emetic is used in nausea and vomiting caused by intracranial tumours

A

dexamethasone

(reduces ICP)

23
Q

Sx of metastasis to bones (x2)

A

pain
pathological fractures
hypercalcaemia
raised ALP ( raised ALP on its own is bone)

24
Q

sx metastasis to brain (x3)

A

headaches
seizures
neuro deficits

25
Q

Sx metastasis of lung cancer

A

cough
SOB
chest pain

26
Q

what are the most common causes of bone mets (x3)

A

descrending order
prostate
breast
lung

Po – Prostate
R – Renal
Ta – Thyroid
B – Breast
Le – Lung

27
Q

what cancers typically metastesis to the lung

A

breast (also common in bone)
colorectal
renal (also common in bone)
bladder
prostate (also common in bone)

28
Q

how do lung mets appear on X-ray

A

cannonball metastases

multiple, round, well-defined lung cancers

most common with renal cell cancer but also choriocarcinoma/prostate

29
Q

what is the monoclonal antibody tumour marker for breast cancer?

A

CA 15-3

30
Q

what is the monoclonal antibody tumour marker for pancreatic cancer?

A

CA 19-9

31
Q

what is the monoclonal antibody tumour marker for ovarian cancer?

A

CA 125

( think of them in order form top to bottom - breast (15-3), pancreas (19-9), ovarian (125))

32
Q

what is the tumour antigen tumour marker for prostatic carcinoma?

A

Prostate specific antigen (PSA)

33
Q

what is the tumour antigen tumour marker for hepatocellular carinomas & teratomas ?

A

alpha-feto protein (AFP)

34
Q

what is the tumour antigen tumour marker for colorectal cancer?

A

carcinoembryonic agent (CEA)

35
Q

what is the tumour antigen tumour marker for melanoma & schwannomas ?

A

S-100

36
Q

what cancer(s) does the tumour antigen bombesin indicate?

A

small cell lung carcinoma
gastic cancer
neuroblastoma

37
Q

how do pathological fractures appear

A

compression fractures and focal sclerotic bony lesions.

38
Q

how do the fractures in bone mets differ to those in Pagets disease of the bone/multiple myeloma on X-ray

A

multiple myeloma/ pagest disease
osteolytic lesions ( loss of bones)

bone mets - sclerotic regions - thick areas of bones

39
Q

apart from metastatic cancer and multiple myeloma, give 2 causes of pathological fractures

A

cancerous: sarcoma

non-cancerous: metabolic:
- osteoporosis,
- hyperparathyroidism

Bone disease
pagets disease

40
Q

what is the most common cause of pathological fractures

A

tumours

41
Q

features suggesting a pathological fracture

A

Pain: localised, severely disproportionate to injury

fracture followign minor trauma

deformity at fracture site

impaired function of affected limb

42
Q

what genetic condition are desmoid tumours associated with

A

Gardners syndrome, mutation of PAPC gene on chromosome 5

desmoid tumours (fibrous growths which occur anywhere in the body) are found in 15% of cases

43
Q
A
44
Q

what is the difference in location between squamous cell lung canrcinomas and lung adenocarcinomas

A

squamous cell - close to large airways “lung nodule in close proximity to his left main bronchus.”

adenocarcinomas: peripheral lung