MSK- orthopaedics and rheumatology Flashcards

(40 cards)

1
Q

What are the seronegative spondyloarthropathies

A

Ankylosing spondylitis
Psoriatic arthritis
IBD related arthritis
Reactive arthritis

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2
Q

Most common primary malignant bone tumour

A

Osteosarcoma
Seen mostly in children and adolescents
Sunburst pattern on xray

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3
Q

Ewing’s sarcoma sign on xray

A

Onion skin appearance

Severe long bone pain

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4
Q

Differentials for polyarteritis

A
Rheumatoid arthritis 
SLE
Seronegative spondyloarthropathies 
Henoch-Schonlein purpura
Sarcoidosis
Tuberculosis
Pseudogout
Viral infection: EBV, HIV, hepatitis, mumps, rubella
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5
Q

Classical Colle’s fracture

A

Fall onto an extended outstretched hand
Transverse fracture of the radius
1 inch proximal to the radio-carpal joint
Dorsal displacement and angulation

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6
Q

Bennett’s fracture

A

Intra-articular fracture of the first carpometocarpal joint

Caused by fist fights

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7
Q

Pott’s fracture

A

Bimalleolar ankle fracture

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8
Q

Blood results in PMR

A

Raised ESR and CRP

Normal CK and anti-CCP

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9
Q

Typical features of PMR

A
Usually patient >60
Association with GCA
Usually rapid onset
Aching, morning stiffness in proximal limb muscles (which may present as weakness but is not true weakness)
Mild polyarthralgia
Lethargy and depression
Low grade fever
Anorexia 
Night sweats
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10
Q

Schober’s test

A

A line is drawn at the level of the ASIS
10cm above and 5cm below
Gap should increase on lumbar flexion by more than 5cm

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11
Q

Management of De Quervain’s tenosynovitis

A

Analgesia
Steroid injection
Immobilisation with a thumb splint
Surgical treatment may be required

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12
Q

Signs of ank spon on Xray

A

Sacroilitis- subchondral erosions and sclerosis (most useful in establishing diagnosis)
Squaring of lumbar vertebrae
Syndesmophytes due to ossification of the annulus fibrosus
Bamboo spine (late stages)
‘Shiny corners’ on MRI

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13
Q

Felty’s syndrome

A

RA
Splenomegaly
Low WCC

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14
Q

Sulfasalazine

A

5-ASA- decreases neutrophil chemotaxis and suppresses lymphocytic prophylaxis

Allergy to sulphonamides

S/E: oligospermia, Stevens-Johnson, pneumonitis/ fibrosis, myelosuppression, anaemia

Considered safe in pregnancy and breast-feeding

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15
Q

Anterior compartment of the lower leg

Innervated by

A

Tibialis anterior
Extensor digitorum longus
Peroneus tertius
Extensor hallucis longus

Deep peroneal nerve

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16
Q

Superficial posterior compartment of the lower leg

Innervated by

A

Gastrocnemius
Soleus

Tibial nerve

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17
Q

Deep posterior compartment of the lower leg

Innervated by

A

Flexor digitorum longus
Flexor hallucis longus

Tibialis posterior

18
Q

Still’s disease in adults

A
Arthralgia 
Elevated serum ferritin
Salmon-pink, maculopapular rash
Pyrexia in a daily pattern- rises in the late afternoon 
Lymphadenopathy 
RF and ANA negative
19
Q

Most common cause of mitral stenosis

A

Rheumatic fever

20
Q

Erythema marginatum

A

Pathognomonic for rheumatic fever
Annular erythematous rash that commonly affects the trunk and inner surfaces of arms and legs and can persist for several months
Non-pruritic rings that are barely raised
Generally spares the face

21
Q

Clinical features of ankylosing spondylitis

A

Young caucasian man in teens or 20s
Sacroiliitis- MRI can show early oedema
Back pain in the night or early morning, especially on inactivity
Unilateral buttock pain that radiates to the groin

22
Q

Complications of ankylosing spon

A

Enphysitis- inflammation between tendon and bone
Costochondritis
Rarely jaw pain
Apical interstitial fibrosis
Fusing of syndesmophytes late stage causes bamboo spine

23
Q

Treatment of ankylosing spondiliitis

A

NSAIDs- ibuprofen and/or naproxen
Exercise
Physiotherapy
If this isn’t successful then biologics can be used- infliximab

24
Q

Management of OA

A

Exercise to improve muscle strength and general aerobic fitness
MDT approach, PT and OT
Heat or cold packs, walking aids and TENS

Analgesia- regular paracetamol and topical NSAIDs, can use codeine or oral NSAIDs if ineffective
Intra-articular steroid injections temporarily relieve pain in severe cases

Surgical- Joint replacement

25
Management of septic arthritis
Which organisms and how did they get there? immunosuppression, CKD, recent surgery, STI, IV drug abuse 2 weeks broad spectrum antibiotics IV until sensitivities are known and then more specific by local guidelines 4 weeks oral Orthopaedic review for athrocentesis, washout and debridement
26
Extra-articular manifestations of rheumatoid arthritis
Nodules- elbow, lungs, cardiac, CNS, lymphadenopathy, vasculitis Lungs- pleural disease, interstitial fibrosis, bronchiolitis obliterans Cardiac- IHD, pericarditis, pericardial effusion Carpal tunnel syndrome Peripheral neuropathy Felty's syndrome Eye- episcleritis, scleritis, scleromalacia, keratoconjunctivitis sicca Osteoporosis Amyloidosis
27
Investigating ?RA
Anti-rheumatoid factor- positive in 70% Anti- citric citrullinated peptide- highly specific (90-95%) FBC- anaemia of chronic disease, raised platelets ESR raised Raised CRP Xrays- loss of joint space, erosions, soft tissue swelling, juxta-articular osteoporosis
28
Management of RA
Disease activity monitoring via DAS28 DMARDs and biological agents (after trialling at least 2 DMARDs) Steroids to bridge, reducing symptoms and inflammation NSAIDs PT and OT
29
Crystals in gout
Monosodium urate
30
Limited systemic sclerosis
Anti-centromere antibodies | Involves the hands, face and feet, pulmonary hypertension is often subclinical
31
What should be screened for in any myositis?
Malignancy- lung, pancreatic, ovarian or bowel | Can often present as a paraneoplastic phenomenon, even before the disease takes hold
32
Clinical features of dermatomyositis
Myositis- symmetrical, proximal muscle weakness Macular rash- heliotrope rash on eyelids often with oedema Nailfold erythema Gottron's papules- pathognomic if raised CK and weakness
33
Differentials for myositis
``` Dermatomyositis Polymyositis Inclusion body myositis Carcinomatous myopathy Muscular dystrophy (Becker's if older) PMR Endocrine/metabolic myopathy Rhabdomyolysis Infection Drugs- penicillamine, colchicine, statins, chloroquine ```
34
Tests for myositis
CK and other muscle enzymes- ALT, AST, LDH, aldolase EMG Muscle biopsy Anti-Mi2 or anti-Jo1
35
Clinical features of systemic lupus erythematosus
Malaise, fatigue, myalgia, fever Lymphadenopathy, weight loss, alopeecia, nail-fold infarcts, Raynaud's Malar rash- flat or raised, sparing of the nasolabial folds, can be photosensitive Oral nasal uclers Synovitis Serositis- pleura or pericardium Haemolytic anaemia- positive direct Coombs test
36
Antibodies in drug induced lupus
Anti-histone
37
Laboratory features of SLE
``` +ANA Anti-dsDNA Anti-smith Low complement C3 and C4 +direct Coombs test Antiphospholipid antibodies in 20-30% ```
38
Management of SLE
MDT, specialist team/ nephritis clinic General measures- high factor sunblock, hydroxychloroquine, screen for co-morbidities and medication toxicity Maintenance- NSAIDs and hydroxychloroquine Also can use methotrexate, azathioprine, mycophenolate or biologics Mild flares- hydroxychloroquine or low dose steroids Moderate may require DMARDs Severe flares- urgent high dose steroids, mycophenolate, rituximab, cyclophosphamide MDT for neuropsychiatric SLE
39
Antiphospholipid syndrome manifestations | HINT: CLOT
Coagulation defect with paradoxical raised APTT Livedo reticularis Obstetric complications- recurrent miscarriage Thrombocytopenia
40
Antiphospholipid antibodies
Anti-cardiolipin Anti glycoprotein Lupus anticoagulant