Common MSK Swellings Flashcards

1
Q

important questions in swelling history?

A
when did it appear - sudden or gradual?
trauma?
painful?
change in size?
systemic symotoms?
anything similar?
what functional problems does it cause?
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2
Q

important examination features of a swelling?

A
site
shape
size
well defined?
consistency - fluctuant?
surface texture
mobile or fixed
temp
transluminable?
skin changes
local lymphadenopathy
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3
Q

history features of an infective cause for swelling?

A
systemic upset
pyrexia
trauma
association with medical co-morbidities
rubor, calor, dolor, tumor
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4
Q

how does cellulitis present?

A

generalised swelling rather than discreet lump
pain
erythema

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5
Q

what commonly causes cellulitis?

A

Beta haemolytic strep

staph

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6
Q

how is cellulitis managed?

A
rest
elevation
analgesia
splint
antibiotics (oral or IV)
- penicillin
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7
Q

presentation of abscesses?

A

discreet collection of pus - defined and fluctuant swelling
erythema
pain
history of trauma

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8
Q

how is an abscess managed?

A
surgical incision and drainage always
rest
elevation
analgesia
splint
antibiotics
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9
Q

what causes septic arthritis?

A

bacterial infection of a joint - trauma or haematogenous spread
staph aureus
strep
E coli

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10
Q

how does septic arthritis present?

A

acute monoarthropathy
reduced ROM +/- swelling
systemic upset
raised WCC + inflammatory markers

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11
Q

how is septic arthritis managed?

A

urgent orthopaedic review
aspiration
urgent open/arthroscopic washout + debridement

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12
Q

what is a ganglia?

A

outpouching of synovium lining of joints and filled with synovial fluid

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13
Q

how does a ganglia present?

A
discreet round swelling
non-tender
<10mm - several cm
skin mobile, fixed to underlying structures
seen in wrists, feet and knees
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14
Q

how is a ganglia managed?

A

nothing
NOT ASPIRATION
percutaneous rupture (hit it)
surgical excision

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15
Q

what is a bakers cyst?

A

cyst/ganglion of the popliteal fossa

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16
Q

how does a bakers cyst present?

A

general fullness of the popliteal fossa
soft and non-tender
associated with OA
painful rupture

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17
Q

how is a bakers cyst managed?

A

non-operative

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18
Q

what is bursitis?

A

inflammation of the synovium lined sacs that protect bony prominences and joints
can become secondarily infected and form an abscess

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19
Q

how is bursitis managed?

A

NSAIDs/analgesia
antibiotics
incision and drainage (if secondary infection)
V. rarely needs excision

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20
Q

what is gout?

A

inflammatory arthritis most commonly affected the great toe but can affect other joints - knee etc
caused by elevated serum urate resulting in a deposition of uric acid crystals in joints

21
Q

what is gout associated with?

A

purine rich food
alcohol
dairy

22
Q

how does gout present?

A

severe pain
red, hot swollen joint
can have acute attacks and chronic progressive joint damage

23
Q

how is gout diagnosed and treated?

A

diagnosis = clinical, aspiration - negatively befringed monosodium urate crystals

24
Q

how is gout managed?

A

NSAIDs
steroids
allopurinol

25
what are rheumatoid nodules?
nodules around joints in RA patients | associated with repetitive trauma
26
how are rheumatoid nodules managed?
don't respond to DMARDs excision of problematic recurrence high
27
Bouchards vs Heberdens nodes?
``` bouchard = PIPs (OA or RA) heberdens = DIPs (only OA) ```
28
what is dupuytrens disease and what causes it?
progressive disease of fascia causing digital flexion contractures excessive myofibril proliferation and altered collagen matrix composition lead to thickened and contracted palmar fascia type 3 collagen bands avascular process involving O2 free radicals
29
3 contributing factors in dupuytens?
``` genetic predisposition (northern Europe, Men > women, AD) environmental factors (alcohol, diabetes, trauma) local and global protein expression ```
30
how is dupuytrens managed?
``` depends on functional impediment needle fasciotomy collagenase injection limited fasciectomy dermofasciectomy + graft ```
31
what is giant cell tumour of the tendon sheath?
regenerative hyperplasia with inflammatory process benign, common don't confuse with giant cell tumour of bone
32
what are the 2 types of GCT of tendon sheath?
localised (common) | diffuse (rare)
33
how does a GCT of tendon sheath present?
slowly enlarging firm discreet swelling on volar aspect of digits can occur in toes may or may not be tender
34
how is GCT of tendon sheath managed?
leave alone if not causing issue | surgical excision if needed (often only marginal excision)
35
what is an osteochondroma?
benign tumour most commonly occurring near the knee (distal femur or proximal tibia) cartilage capped ossified pedicle
36
how does osteochondroma present?
``` hard, painless lump growth parallel to the patient pain and numbness on activity can rarely get pain from a fracture occurs in adolescence can have multiple tumours in multiple hereditary exostosis ```
37
malignant potential in osteochondroma?
<1% | 5% in multiple hereditary exostosis
38
how is osteochondroma managed?
close observation | surgical excision if needed
39
what is ewings sarcoma?
malignant primary bone tumour of the endothelial cells in the marrow usually occurs at the diaphysis/metaphysis of long bones and pelvis
40
how does ewings sarcoma present?
hot swollen tender joint or limb with raised inflammatory markers (mimics infection) ask about night pain and duration of symptoms
41
how is ewings sarcoma managed?
poor prognosis surgical excision difficult often chemo and radio sensitive
42
what is a lipoma?
benign neoplastic proliferation of fat | often subcutaneous
43
how does a lipoma present?
``` can be discreet or less well defined slow growing and painless can be large soft, moveable mass no overlying skin changes ```
44
how is a lipoma managed?
based on symptoms can be left alone surgical excision if causing symptoms
45
what is a sebaceous cyst and how does it present?
originate at the hair follicle and fill with caseous keratin slow growing, painless, mobile discreet swellings can become infected
46
how are sebaceous cysts managed?
excision if required
47
what is myositis ossificans?
abnormal calcification of a muscle haematoma | usually initial trauma > initial small swelling > hardness develops over several weeks
48
how is myositis ossificans diagnosed and managed?
diagnosis = X ray and MRI showing peripheral mineralisation management - observation - only intervene if symptoms - must wait until maturity of ossification otherwise risk of recurrence (6-12 months)