rheum Flashcards

(56 cards)

1
Q

acute Gout

A

NSAIDs
colchicine if renal impairment
3rd line steroids oral
4th intraarticular steroids

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2
Q

DE QUERVEINS Tendosinovitis

A

Features
pain on the radial side of the wrist
tenderness over the radial styloid process
abduction of the thumb against resistance is painful
Finkelstein’s test: with the thumb is flexed across the palm of the hand, pain is reproduced by movement of the wrist into flexion and ulnar deviation

Management
analgesia
steroid injection
immobilisation with a thumb splint (spica) may be effective
surgical treatment is sometimes required
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3
Q

OSteoporosis frax

A
FRAX:
history of glucocorticoid use
rheumatoid arthritis
alcohol excess
history of parental hip fracture
low body mass index
current smoking
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4
Q

Marfan’s assw what eye condition

A

eyes: upwards lens dislocation (superotemporal ectopia lentis), blue sclera, myopia

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5
Q

rheumatoid arthritis what drugs are safe in pregnancy

A

sulfasalazine

hydroxychloroquine

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6
Q

rheumatoid factor

A

IgM towards one’s own IgG

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7
Q

Marfan’s mutation

A

Mutation of FBN1 that encodes Fibrillin-1

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8
Q

sjogren’s assw with what malignancy

A

lymphoid malignancy

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9
Q

anti-Jo 1:

A

polymyositis

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10
Q

anti centromere antibodies

A

Limited (central) systemic sclerosis = anti-centromere antibodies

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11
Q

Limited cutaneous systemic sclerosis

A

Raynaud’s may be first sign
scleroderma affects face and distal limbs predominately
associated with anti-centromere antibodies
a subtype of limited systemic sclerosis is CREST syndrome: Calcinosis, Raynaud’s phenomenon, oEsophageal dysmotility, Sclerodactyly, Telangiectasia

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12
Q

scl 70 antibodies

A

Diffuse cutaneous systemic sclerosis

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13
Q

Diffuse cutaneous systemic sclerosis

A

scleroderma affects trunk and proximal limbs predominately
associated with scl-70 antibodies
the most common cause of death is now respiratory involvement, which is seen in around 80%: interstitial lung disease (ILD) and pulmonary arterial hypertension (PAH)
other complications include renal disease and hypertension
poor prognosis

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14
Q

Scleroderma

A

(without internal organ involvement)
tightening and fibrosis of skin
may be manifest as plaques (morphoea) or linear

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15
Q

azathioprine

A

metabolised to the active compound mercaptopurine, a purine analogue that inhibits purine synthesis. A thiopurine methyltransferase (TPMT) test may be needed to look for individuals prone to azathioprine toxicity.

Adverse effects include
bone marrow depression
nausea/vomiting
pancreatitis
increased risk of non-melanoma skin cancer
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16
Q

Ankylosing spondylitis - x-ray findings:

A

subchondral erosions, sclerosis
and squaring of lumbar vertebrae

late:
sacroiliitis: subchondral erosions, sclerosis
squaring of lumbar vertebrae
‘bamboo spine’ (late & uncommon)
syndesmophytes: due to ossification of outer fibers of annulus fibrosus
chest x-ray: apical fibrosis

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17
Q

proximal myopathy in combination with mechanic hands

A

anti-synthetase syndrome.

association with interstitial lung disease - particularly non-specific interstitial pneumonia or NSIP.

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18
Q

Mx of Sjogrens

A

artificial saliva and tears

pilocarpine may stimulate saliva production

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19
Q

polyarteritis nodosa

A

fever, malaise, arthralgia
weight loss
hypertension
mononeuritis multiplex, sensorimotor polyneuropathy
testicular pain
livedo reticularis
haematuria, renal failure
perinuclear-antineutrophil cytoplasmic antibodies (ANCA) are found in around 20% of patients with ‘classic’ PAN
hepatitis B serology positive in 30% of patients

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20
Q

Reactive arthritis: features

A

typically develops within 4 weeks of initial infection - symptoms generally last around 4-6 months
arthritis is typically an asymmetrical oligoarthritis of lower limbs
dactylitis
symptoms of urethritis
eye: conjunctivitis (seen in 10-30%), anterior uveitis
skin: circinate balanitis (painless vesicles on the coronal margin of the prepuce), keratoderma blenorrhagica (waxy yellow/brown papules on palms and soles)

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21
Q

biggest cause of gout

A

decrease in renal urate secretion:
drugs*: diuretics
chronic kidney disease
lead toxicity

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22
Q

Rheumatoid arthritis Mx

A

DMARD monotherapy plus bridging steroids

methotrexate is the most widely used DMARD. Monitoring of FBC & LFTs is essential due to the risk of myelosuppression and liver cirrhosis. Other important side-effects include pneumonitis
sulfasalazine
leflunomide
hydroxychloroquine

if 2 dmards fail - can try TNFalpha inhibitor
- infliximab

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23
Q

Paget’s blood and urine

A

raised ALP
normal calcium and phosphate

Raised urine hydroxyproline - bone turnover

24
Q

examination of carpal tunnel syndrome

A

weakness of thumb abduction (abductor pollicis brevis)
wasting of thenar eminence (NOT hypothenar)
Tinel’s sign: tapping causes paraesthesia
Phalen’s sign: flexion of wrist causes symptoms

25
ankylosing spondilitis
if using TNF alpha inhibitors | - radiological progression is NOT changed
26
L3 nerve root compression
loss of thigh sensation reduced knee reflex positive femoral stretch test weakness of quadriceps
27
L4 nerve root compression
Sensory loss anterior aspect of knee Weak quadriceps Reduced knee reflex Positive femoral stretch test
28
L5 Nerve compression
Sensory loss dorsum of foot Weakness in foot and big toe dorsiflexion Reflexes intact Positive sciatic nerve stretch test
29
S1 nerve root compression
Sensory loss posterolateral aspect of leg and lateral aspect of foot Weakness in plantar flexion of foot Reduced ankle reflex Positive sciatic nerve stretch test
30
pseudogout
Features knee, wrist and shoulders most commonly affected joint aspiration: weakly-positively birefringent rhomboid-shaped crystals x-ray: chondrocalcinosis Management aspiration of joint fluid, to exclude septic arthritis NSAIDs or intra-articular, intra-muscular or oral steroids as for gout ``` RF haemochromatosis hyperparathyroidism acromegaly low magnesium, low phosphate Wilson's disease ```
31
Symptoms may be reproduced by deep palpation just below the ASIS (pelvic compression) and also by extension of the hip. There is altered sensation over the upper lateral aspect of the thigh. There is no motor weakness.
? meralgia paraesthetica - lateral cutaneous nerve of thigh compression Burning, tingling, coldness, or shooting pain Numbness Deep muscle ache Symptoms are usually aggravated by standing, and relieved by sitting They can be mild and resolve spontaneously or may severely restrict the patient for many years.
32
antiphospholipid syndrome
``` Features venous/arterial thrombosis recurrent fetal loss livedo reticularis thrombocytopenia prolonged APTT other features: pre-eclampsia, pulmonary hypertension ``` Associations other than SLE other autoimmune disorders lymphoproliferative disorders phenothiazines (rare)
33
sulfasalazine cautions + adverse effects
G6PD deficiency allergy to aspirin or sulphonamides (cross-sensitivity) Adverse effects oligospermia Stevens-Johnson syndrome pneumonitis / lung fibrosis myelosuppression, Heinz body anaemia, megaloblastic anaemia may colour tears → stained contact lenses
34
which TB drug causes lupus
isoniazid
35
weak external rotation of shoulder
adhesive capsulitis
36
Anti-ribonuclear protein (anti-RNP)
mixed connective tissue disease
37
Rheumatoid arthritis XR changes
Early x-ray findings loss of joint space juxta-articular osteoporosis soft-tissue swelling Late x-ray findings periarticular erosions subluxation
38
Rheumatoid arthritis associations
respiratory: pulmonary fibrosis, pleural effusion, pulmonary nodules, bronchiolitis obliterans, methotrexate pneumonitis, pleurisy ocular: keratoconjunctivitis sicca (most common), episcleritis, scleritis, corneal ulceration, keratitis, steroid-induced cataracts, chloroquine retinopathy osteoporosis ischaemic heart disease: RA carries a similar risk to type 2 diabetes mellitus increased risk of infections depression Less common Felty's syndrome (RA + splenomegaly + low white cell count) amyloidosis
39
Temporal arteritis features
Temporal arteritis is large vessel vasculitis overlaps with polymyalgia rheumatica (PMR). Features typically patient > 60 years old usually rapid onset (e.g. < 1 month) headache (found in 85%) jaw claudication (65%) visual disturbances secondary to anterior ischemic optic neuropathy tender, palpable temporal artery around 50% have features of PMR: aching, morning stiffness in proximal limb muscles (not weakness) also lethargy, depression, low-grade fever, anorexia, night sweats
40
Temporal arteritis Ix Rx
Investigations raised inflammatory markers: ESR > 50 mm/hr (note ESR < 30 in 10% of patients). CRP may also be elevated temporal artery biopsy: skip lesions may be present note creatine kinase and EMG normal Treatment high-dose prednisolone - there should be a dramatic response, if not the diagnosis should be reconsidered urgent ophthalmology review. Patients with visual symptoms should be seen the same-day by an ophthalmologist. Visual damage is often irreversible
41
Usually gradual onset Unilateral or bilateral leg pain (with or without back pain), numbness, and weakness which is worse on walking. Resolves when sits down. Pain may be described as 'aching', 'crawling'. Relieved by sitting down, leaning forwards and crouching down Clinical examination is often normal Requires MRI to confirm diagnosis
Spinal stenosis
42
bone protection in long term steroids
T score Management Greater than 0 Reassure Between 0 and -1.5 Repeat bone density scan in 1-3 years Less than -1.5 Offer bone protection
43
initially intermittent tingling in the 4th and 5th finger may be worse when the elbow is resting on a firm surface or flexed for extended periods later numbness in the 4th and 5th finger with associated weakness
Cubital tunnel syndrome Due to the compression of the ulnar nerve.
44
chronic pain: at multiple site, sometimes 'pain all over' lethargy cognitive impairment: 'fibro fog' sleep disturbance, headaches, dizziness are common
fibromyalgia polymyalgia rheumatica presents similar but with fevers and weight loss
45
low: calcium, phosphate raised: alkaline phosphatase
osteomalacia
46
The classic laboratory finding is a raised creatinine kinase (CK) and the Anti-Jo-1 antibody
The hallmark of polymyositis is weakness and/or loss of muscle mass in the proximal musculature, and absent skin involvement. ``` proximal muscle weakness +/- tenderness Raynaud's respiratory muscle weakness interstitial lung disease: e.g. fibrosing alveolitis or organising pneumonia dysphagia, dysphonia ```
47
anti ro
assw congenital heart block | assw SLE and sjogrens
48
Osteoarthritis
- paracetamol + topical NSAIDs (if knee/hand) first-line
49
Repeated cramping and myoglobinuria after short bouts of exercise
McArdle's disease Overview autosomal recessive type V glycogen storage disease caused by myophosphorylase deficiency this causes decreased muscle glycogenolysis ``` Features muscle pain and stiffness following exercise muscle cramps myoglobinuria low lactate levels during exercise ```
50
Pseudoxanthoma elasticum
inherited condition (usually autosomal recessive*) characterised by an abnormality in elastic fibres Features retinal angioid streaks 'plucked chicken skin' appearance - small yellow papules on the neck, antecubital fossa and axillae cardiac: mitral valve prolapse, increased risk of ischaemic heart disease gastrointestinal haemorrhage
51
negatively birefringent crystals in joint aspiration
gout
52
Oral ulcers + genital ulcers + anterior uveitis
Behcet's ``` assw DVT aseptic meningitis arthritis abdo pain/diarrhoea/colitis erythema nodosum ```
53
DIP involvement arthritis
psoriatic
54
hydroxychloroquine SE
retinopathy
55
bone pain, typically in the skull or proximal femur cutaneous nodules recurrent otitis media/mastoiditis tennis racket-shaped Birbeck granules on electromicroscopy
Langerhans cell histiocytosis is a rare condition associated with the abnormal proliferation of histiocytes. It typically presents in childhood with bony lesions.
56
erythematous, raised rash, sometimes scaly may be photosensitive more common on face, neck, ears and scalp lesions heal with atrophy, scarring (may cause scarring alopecia), and pigmentation
Discoid lupus erythematosus benign disorder younger females. rarely progresses to systemic lupus erythematosus (in less than 5% of cases). Discoid lupus erythematosus is characterised by follicular keratin plugs and is thought to be autoimmune in aetiology Management topical steroid cream oral antimalarials may be used second-line e.g. hydroxychloroquine avoid sun exposure