Revision for MCQ's Flashcards

1
Q

What is the most common skin cancer in nz? What are the risk factors?

A

BCC: Fair skin, age and sun exposed places.

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2
Q

What is the most important prognostic factor in melanoma? What is second?

A

Depth. Lymph node involvement.

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3
Q

What is 1% of body equal to?

A

The palm of the hand and fingers of the patient.

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4
Q

What is the fluid requirement for a burn?

A

3-4mls/kg/% burn over 24 hours of heartmans. Give half in the first 8 hours.

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5
Q

What is a flap vs a graft?

A

A flap has its own blood supply. A graft needs a blood supply (and cant be put on avascular tissue such as cortical bone or tendons).

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6
Q

What are the two types of flaps? Explain the difference.

A

Split thickness (SSG) and full thickness graft (FFSG).
SSG doesn’t contain the underlying deep dermis therefore doesn’t contain sweat glands etc, but a large chunk can be taken as it leaves the skin on top for the donor to epithelialise. FFSG need to be closed fully and only a small amount can be taken - but it does contain sweat glands and doesn’t look shiny.

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7
Q

What is a compound graft/flap.

A

A flap/graft with lots of different tissue types e.g. skin fat and cartilage.

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8
Q

What is a microvascular flap/free flap?

A

A flap which has been disconnected from blood supply but then reconnected using microsurgical techniques.

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9
Q

Does a craniosynostosis need an xray?

A

No

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10
Q

What are some issues with craniosynostosis?

A
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11
Q

How are most craniosynostosis treated?

A

With springs.

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12
Q

What joints are effected in RA?

A

preferentially the wrist, MCP and PIP joints.

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13
Q

What blood tests are specific and sensitive for RA?

A

Blood tests: CRP and ESR are increased.
RF is increased - but not specific.
AntiCCP is much more specific (90%).

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14
Q

What genetic marker is altered in RA?

A

HLA - DR4 (found in 70% of patients and is associated with bad outcomes). HLA - DR1 is also a good marker.
PTPN22 and PAD14.

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15
Q

What increases risk of RA?

A

Smoking (lots of citrullinated proteins) increases risk for rheumatoid +vs RA patients.

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16
Q

What is the key pathophysiological feature of RA?

A

Thickend, inflammed, hypervascular and hypercellular synovium creating a pannus of lymphocytes.

17
Q

Drugs to treat RA?

A

NSAIDS for symptoms. Prednisone to get inflammation down early. Methotrexate or sulphasalazine as a DMARD.
Methotrexate is a teratogen so don’t use if pregnant or planning to get pregnant - maybe put on adequate contraceptive. Hydroxychloroquine can be given in this case.
Can go onto biologics such as infliximab (anti-TNF)

18
Q

What is the goal serum urate level to get down to

A

0.36mmol/L.

19
Q

Treatment of gout?

A
  1. NSAIDS but they are often contraindicated.
  2. Cholchine but contraindicated in eGFR <50
  3. Corticosteroids if anything else doesn’t work 20-40mg of pred stat, then daily and wean over 2 weeks to prevent another attack.
20
Q

What are the guidelines for giving urate lowering drugs?

A

1) at least 2 flares every year.
2) a tophus present (extra-articular collections of cells and urate crystals in soft tissue).
3) x-ray evidence of damage from gout.
4) renal impairment or very high urate.

21
Q

How does allopurinol work?
Are there side effects?

A

Xanthine oxidase inhibitor.
Lots of side effects - severe hypersensitivity reaction.
Need to do blood tests to look for kidney function before giving as oxypurinol may cause this hypersensitivity reaction.

22
Q

Symptoms of PMR?

A

Pain in shoulder and pelvic girdle.

23
Q

What test is normally high in PMR?

A

ESR and CRP.

24
Q

What are some differentials for PMR

A

Fibromyalgia, rheumatoid arthritis, malignancy and hypothyroidism.

25
Q

How do you treat PMR?

A

Low dose steroid: 15mg of prednisone daily for 1mth then slowly taper off till you find the perfect dose. Most patients will require low dose prednisone for 3 years.

26
Q

What do you need to look out for with PMR?

A

Temporal arteritis: red flags are fever, loss of vision, new headaches in temporal region. superficial temporal arteries may be tender/pulseless.
Need to treat with steroids (80mg pred) to prevent permanent blindness.
Always do a temporal artery biopsy.

27
Q

What is the main gene indicated in spondyloarthropathies?

A

HLAB27

28
Q

What things make spondyloarthropaties feel better?
What makes spondyloarthropaties worse?

A

1) improvement with movement/exercise
2) Improvement with NSAID treatment.

1) Pain with rest/going to bed.

29
Q

What is enthesis? What is normally affected in ankspond?

A

Pain at the insertion site of a tendon into the periosteum. The archillies tendon and plantar fascia.

30
Q

What are the extraarticular features of spondyloarthropathies?

A

Anterior uveitis in 25%
IBD in 7%
Lung fibrosis or pneumonitis.
Cardiac conduction defecits.