rheum passmed year 5 Flashcards

1
Q

when is denosumab used in OP tx

A

after bsiphospphonate tried - two different types

or if renal function is under 30

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2
Q

methotrexate toxicity tx

A

Folinic acid

antidote to folic acid antagonists (ie, methotrexate and pyrimethamine)

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3
Q

livedo reticularis caused by what thrombotic disease

A

anitphospholipid syndrome

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4
Q

primary thromboprophylaxis
in antiphsipholipid syndrome

A

low dose aspirin

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5
Q

Psoriatic arthropathy is an inflammatory arthritis associated with psoriasis and is classed as one of the seronegative spondyloarthropathies. It correlates poorly with cutaneous psoriasis and often precedes the development of skin lesions
what is MX

A

methotrexate

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6
Q

where do ewing sarcomas arise

A

Ewing sarcoma typically occurs in the diaphysis or metaphyseal–diaphyseal portion of long bones

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7
Q

what is the periosteum

A

The periosteum is the medical definition for the membrane of blood vessels and nerves that wraps around most of your bo

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8
Q

what is a periosteal reaction

A

eriosteal reaction results when cortical bone reacts to one of many possible insults. Tumor, infection, trauma, certain drugs, and some arthritic conditions can elevate the periosteum from the cortex and form various patterns of periosteal reaction

seen in ewing

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9
Q

Chondrosarcoma - cartilage - normally affects where

A

axial skeleton - skull, v body, rib cage pelvis

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10
Q

osteosarcoma occurs where and pre what

A

occurs most frequently in the metaphyseal region of long bones prior to epiphyseal closure.

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11
Q

causes of drug induced lupus

A

Most common causes
procainamide
hydralazine

Less common causes
isoniazid
minocycline
phenytoin

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12
Q

when do you lower your dose of aziothiopurine

A

A significant interaction may occur with allopurinol and hence lower doses of azathioprine should be used.

preg keep same as safe

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13
Q

how does haemachromatosis lead to psedogout

A

Hemochromatosis (HH) is a condition that can cause calcium pyrophosphate (CPP) crystal deposition in the joints, which is also known as pseudogout. The exact mechanism that causes CPP crystal formation in HH patients is not fully understood, but some studies suggest that iron may play a role:

Iron damage: Excess iron can damage bone cells and chondrocytes.

Osteoclastogenesis: Iron may stimulate osteoclastogenesis, which is associated with premature and severe CPPD

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14
Q

A postmenopausal woman who’s had an osteoporotic vertebral fracture should be started on a bisphosphonate straight away

A

true

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15
Q

GCA suspected given high dose oral pred - temp biopsy done but comes back normal what to do next and why

A

Continue high-dose prednisolone and repeat biopsy as Skip lesions occur in giant cell arteritis and may show a normal biopsy

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16
Q

two movement associated with lateral epicondylitis

A

worse on resisted wrist extension/suppination whilst elbow extended

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17
Q

pagets( increased uncontrolled bone turnover) tx

A

bisphosphonate (either oral risedronate or IV zoledronate)

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18
Q

pANCA may be positive in which crohns or UC

A

pANCA may be positive in UC, but will likely be negative in Crohn’s

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19
Q

in septic arthritis what IX is important to do before giving abx

A

synovial fluid sampling is obligatory
this should be done prior to the administration of antibiotics if necessary

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20
Q

peptic ulcers contradict what drug

A

NSAID
steriod

21
Q

polymorphonuclear neutrophil predominance

A

RA

22
Q

reactive a. - synovial fluid appears how

A

Sterile synovial fluid with a high white blood cell count

23
Q

household bound pt what should they have

A

vitamin d

24
Q

what are we worried about in people with marfans which is why we do echocardiography

A

dilation of the aortic sinuses which may predispose to aortic dissection

25
Q

Before giving a bisphos what do you need to make sure is checked and corrected if low

A

calclium

and then give bsipho and vit d and maybe Ca (dietary)

26
Q

if pt with polymyaglia rheymatica do not repsond to steriods what do you do

A

cosnider other dx

27
Q

finger swelling - dactylitis feature of what arthritis

A

psoriasitic

28
Q

in gout under what level of uric acid should you measure again 2 weeks later after flare has settled

A

360

29
Q

in women when should they be started on bisphos straight away

A

osteoporotic vertebral fracture in postmenopausal women - dont wait fro dexa

or if over 50 and post on PO steriods

30
Q

acute gout tx for future recurrence

A

allopurinol

colchine for flare

31
Q

Proximal muscle weakness + raised CK + no rash

A

polymyositis

rheumatica raised ESR

32
Q

XR findings in ank spond

A

x-ray findings: subchondral erosions, sclerosis
and squaring of lumbar vertebrae

33
Q

Bone pain, tenderness and proximal myopathy (→ waddling gait)

A

osteomalacia

rickets kids

34
Q

acute flares of RA managed how

A

flares of RA are often managed with corticosteroids - oral or intramuscular

35
Q

what needs to be checked with methotrexate

A

FBC & LFTs i

36
Q

reflex tachycardia is caused by what drug and what is the mech

A

nifidipine

Nifedipine causes peripheral vasodilation which leads to the heart compensating for the drop in blood pressure by beating faster.

37
Q

dermatomyositis what rash is seen over the knuckles

A

Gottron’s papules, roughened red papules over the knuckles mainly

38
Q

A 37-year-old man sees his GP complaining of ‘a flu that won’t go away’. On further questioning he has had a 2-week history of fever, nausea and vomiting, myalgia and weakness, and a sensation of itchiness. He also describes a few episodes of red urine. He denies any cough, haemoptysis or any other respiratory symptoms. On examination you notice he has some slight scleral icterus, alongside small palpable purpura on his lower legs and arms.

Given these features, which of the following would be the most likely diagnosis?

A

The stem may seem overwhelming at first but breaking it down will help reveal clues to the question. His symptoms/signs appear to be rather viral, with the exception of the itchiness, scleral jaundice, haematuria, and purpura. With the systemic symptoms alongside the haematuria and purpura the first thought should be vasculitis, thus eliminating polymyalgia rheumatica.

The scleral jaundice and itchiness suggest a obstructive hepatic impairment. Alongside this, we are also told that the patient has not had any respiratory symptoms. Combining these would help exclude a further three answers and lead to the correct answer of polyarteritis nodosa, which is strongly associated with hepatitis B infection and does not tend to have respiratory features unlike the other 3 vasculitides.

39
Q

hep b associated with what condition

A

polyarteritis nodosa

40
Q

what is PTH raised in osteomalacia and rickets

A

Raised ALP and PTH and decreased calcium and phosphate are incorrect as this is caused by osteomalacia/rickets. This is a condition characterised by impaired mineralization of bone and has several causes such as vitamin D deficiency, liver disease. PTH is raised in an attempt to increase calcium stores for bone mineralisation, leading to increased PTH and ALP.

41
Q

difference between methotrexate and felty syndrome with blood results and splenomegaly or not

A

Felty’s syndrome is a condition characterized by splenomegaly and neutropenia in a patient with rheumatoid arthritis. Hypersplenism results in destruction of blood cells which classically results in neutropenia but can also cause pancytopenia.

methotrexate would not cause splenomegaly

42
Q

long term steriod use what do you need to also be taking immediately

A

bisphosphonates

Start oral alendronate + ensure calcium and vitamin D replete

43
Q

In newly-diagnosed active rheumatoid arthritis what should you tx with

A

with methotrexate (or sulfasalazine or leflunomide) and oral steroids.

Steroids (oral or intra-articular) can be used to alleviate flares, and patients are often also prescribed paracetamol for pain relief.

44
Q

is obesity a risk factor for OP

A

no

45
Q

malignant tumour that occurs most frequently in the diaphysis of the pelvis and long bones

A

ewings tumour - onion skin

46
Q

chrondrosarcoma commonly affects where

A

axial skeleton - and in middle age people

47
Q

osteoma are benign and commonly occur where

what condition are they associated with

A

skull

This condition is also classically associated with Gardner’s syndrome (a variant of familial adenomatous polyposis, FAP).

48
Q

most common benign bone tumour.

cartilaged capped projection

A

Osteochondroma

49
Q

osteosaroma associated with what gene

A

retinoblastoma gene (and hence retinoblastoma tumours).