Rheumatology Flashcards

1
Q

symptoms of reactive arthritis

A

conjunctivitis
arthritis
urethritis

“Can’t see, can’t pee, can’t stand on one knee”

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2
Q

features of polymyositis

A

proximal muscle weakness and wasting
problems getting out of chairs/walking up stairs
can also have oesophageal dysmotility problems and sclerodactyly
low grade fever

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3
Q

Ix for polymyositis

A

anti-Jo antibodies
raised CK
ANA positive

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4
Q

anti-Jo association

A

polymyositis

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5
Q

anti-Ro associations

A

Sjogren’s, SLE, congenital heart block

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6
Q

anti-La association

A

Sjogren’s syndrome

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7
Q

anti-scl-70 association

A

diffuse cutaneous systemic sclerosis

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8
Q

anti-centromere association

A

limited cutaneous systemic sclerosis (CREST syndrome)

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9
Q

symptoms in limited cutaneous systemic sclerosis

A
CREST
calcinosis
raynaud's
oesophogeal dysmotility
sclerodactyly
telangectasia
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10
Q

areas affected in limited cutaneous systemic sclerosis

A

face, forearms and lower legs

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11
Q

diseases predisposing to osteoporosis

A
endo: cushings, GH def, hyperthyroid, hypogonadism (Turner's syn, testosterone def), hyper PTH
GI: IBD, malabsorption, liver disease
multiple myeloma, lymphoma
CKD
RA
osteogenesis imperfecta, homocystinurea
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12
Q

OA Mx

A

weight loss, exercise
1: paracetamol and topical NSAID (for knee/hand)
2: oral NSAID/COX2i + PPI, opiods, capsaicin cream
non pharm: supports, TENS

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13
Q

secondary causes of Raynaud’s phenomenon

A

CT dz: scleroderma (most common), RA, SLE,
type I cryoglobulinaemia, cold agglutinins
OCP
use of vibrating tools (hand-arm vibration syndrome)

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14
Q

Mx of raynauds

A

calcium channel blocker eg nifedipine

IV prostacyclin infusions - last several weeks/months

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15
Q

pathology behind Paget’s disease

A

increased and uncontrolled bone turnover

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16
Q

RFs for Paget’s disease

A

increasing age
male
increased latitude
FH

17
Q

clinical features of Paget’s disease?

A
bone pain (lumbar spine, femur, pelvis)
raised ALP - calcium and phos are typically normal
classically untreated: bowing of tibia, bossing of skull
18
Q

indication for Rx of Pagets and what is the Rx

A

bone pain, fracture, skull or long bone deformity, periarticular Pagets
bisphosphonates (eg risedronate)
calcitonin (less commonly used now)

19
Q

complications of Pagets

A

deafness (CN entrapment)
high output cardiac failure
fracture
osteosarcoma

20
Q

classical history of ankylosing spondylitis

A

25 yo male with insidious onset lower back pain and stiffness that is worse in the morning and improves with exercise. He gets pain at night which improves when he gets up

21
Q

features of Ank Spond

A
reduced chest expansion and lumber flexion
apical fibrosis
anterior uveitis
aortitis
achilles tendonitis
amyloidosis
arthritis (peripheral)
22
Q

cANCA association

A

Wegener’s in >90%

23
Q

pANCA association

A

immune crescentic glomerulonephritis (80%)
microscopic polyangitis (60%)
Churg-Strauss syn (60%)
primary sclerosing cholangitis (70%)

24
Q

Anti-cyclic citrullinated peptide antibody association

A

Rheumatoid Arthritis - detectable 10 yrs before symptomatic

25
Q

conditions with positive RF

A
RA 70-80%
Sjogrens 100%
Felty's syn 100% (RA, neutropenia, splenomegaly)
infective endocarditis 50%
SLE 25%
systemic sclerosis 30%
general population 5%
26
Q

classical triad of Behcet’s syndrome

other Sx

A
1: oral ulcers, 2: genital ulcers, 3: uveitis
thrombophlebitis
arthritis
GI: abdo pain, diarrhoea, colitis
erythema nodosum, DVT
27
Q

features of Churg-Strauss syndrome

A

Allergic phase - asthma or allergic rhinitis
Eosinophilic phase - hypereosinophilia, causing abdominal pain, GI bleeding, night sweats
Vasculitic phase - RF, abdo or heart problems
~50% die from cardiac disease, eosinophilic coronary myocarditis

28
Q

Mx of Churg-Strauss

A

glucocorticoids. 20% need cytotoxics (azathioprine and cyclophosphamide)

29
Q

Most common organism causing septic arthritis

Mx

A

staph. aureus
Mx - synovial aspiration and culture.
fluclox and fusidic acid (clinda if pen allergic) - 2wks IV, 4 weeks PO
May need surgical wash out or repeat aspirations
If young monoarthritis - think gonococcus (10/7 ceftriaxone)
if older/immunosuppressed - ?listeria ?gram neg. Taz instead of fluclox

30
Q

What is Schirmer’s test?

What does it test for?

A

Litmus paper in lower eyelid, Sjögren’s syndrome

Positive if <5mm in 5mins

31
Q

What is Takayasu arteritis?

A

granulomatous vasculitis of large vessels, with intimal fibrosis
Sx: TIAs, claudication, hypertension (renal artery stenosis)
Mx: steroids

32
Q

Which bacterial infection is linked with RA in susceptible individuals?

A

Proteus mirabilus - urine infections.

33
Q

Mx of Ank Spond

A

NSAIDs and physio in early disease
sulphasalazine improves peripheral joint arthritis
later TNF-a antagonists (eg etanercept) can be used.

34
Q

Risk factors for avascular necrosis

A

lupus, steroids, antiphospholipid syndrome, sickle cell disease, alcoholism
Caisson’s disease (decompression sickness “the bends”)
Gaucher’s disease (genetic lipid accumulation disease)

35
Q

Indication for starting osteoporosis treatment following DEXA scan

A

T score < -2.5 in normal adults or < -1.5 in patients on steroids.
Oral bisphosphonates used 1st line.

36
Q

Mx of Feltys syndrome

A

(hepatosplenomegaly, RA and neutropenia)
pulsed corticosteroid and/or cyclophosphamide
splenectomy if medical Rx fails.