MSK Flashcards

1
Q

What are the types of bone tumours?

A

Metastatic disease

Primary bone tumours

Benign

Haematological

Soft tissue bone tumours

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2
Q

Which cancers most likely metastasise to bone?

A
BLT KP
Breast
Lung
Thyroid-TFTs
Kidney-U&E, Ca2+ and Phosphate
Prostate-PSA and DRE
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3
Q

What could be seen on x-ray of bone malignancy?

A
- Locatoion 
Epiphysis?
Metaphysis?
Diaphysis?
- Size
- Lytic or scleroitic?
Sclerotic: prostate as increased osteoclast action
Lytic: Lung, Kdney and Thyroid
Breast is mixed
- Zone of transition
Narrow: slow-growing tumours have well defined demarcated sclerotic margin
Wide: tumour grows too fast for bone to respond-looks moth-eaten
- Periosteal reaction?
- Soft tissue involvement?
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4
Q

What are the primary bone sarcomas?

A
Bone-forming tumours
Cartilage forming tumours
Giant-cell tumour
Marrow tumour
Vascular tumours
CT tumours
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5
Q

What are the characteristics of malignant bone tumours?

A

Poorly defined borders

Wide zone transition

Moth eaten pattern of bone destruction

Periosteum shows interrupted sunburst or onion skin reaction

Adjacent soft tissue mass

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6
Q

What are the characteristics of benign bone tumours?

A

Well-defined sclerotic borders

Geographic bone destruction

Periosteal reation is uninterrupted (solid)

No soft tissue mass

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7
Q

What is osteosarcoma?

A

Malignancy of osteoblasts producing osteoid (immature bone)

Aggressive

Often at end of long bones e.g. the knee

Pain and swelling, may be reluctant to bear weight

Males > females
Teenagers
Paget’s disease
MCC primary bone cancer

Chemo/Radio/Resect

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8
Q

What is Ewing’s sarcoma?

A

Malignant small, round, blue cell tumour of neural tube
Mixed lysis and sclerosis
Pariosteal reaction with lamellated bone growth

Genetic

Fevers, anaemia, systemic illness
May mimic osteomyelitis

55% in axial skeletonPelvis, femur, humerus, ribs and claical and spine
- Spine stenosis, back pain and cauda equina

Teenagers 10-20
Males>females

Chemo/Radio/Surgery

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9
Q

What is chondrosarcoma?

A

Cancer of cartilage producing cells.

Any age-middle and olver

Axial skeleton, pelvis and proximal femur

Xray shows invasion and soft tissue extension

Back or thigh pain, sciatic, bladder problems

Surgical resection (C&R not effective)

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10
Q

What is osteochondroma?

A

MC benign tumour of bone

Cartilage-capped boney projections

Remove if iminging on vessles or nerves and affecting movement

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11
Q

Define: sarcoma

A

Cancer arising from transformed cells fo mesenchymal origin e.g. cancellous bone, cartilage, fat, muscle, vessles or haemopoetic tissue

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12
Q

What may a mid-humeral shaft fracture damage?

A

Radial nerve in the radial groove

Reduced sensation of the dorsal hand and extensor disfunction

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13
Q

Which carpal bone dislocates most commonly?

A

Lunate bone dislocates anteriorly into the carpal tunnel and compresses the median nerve resulting in wrist pain and altered sesnation in the palmar aspect of the lateral fingers and weakness in thumb opposition

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14
Q

Describe a Hamate fracture

A

Usually the hook

Foosh

Damage to the ulnar nerve - claw hand

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15
Q

Describe an Ulnar Collateral Ligament tear

A

‘Skier’s thumb’

Tearing: pain along ulnar side of the MCP thumb joint

Laxity: ‘gamekeeper’s thumb’

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16
Q

What are the risk factors for AVN of the femoral hip?

A

Chronic corticosteroids
Alcohol
SLE

Not many xray changes

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17
Q

What is Septic Arthritis?

A

Pain at rest and movement
Joint (unilateral) tenderness and swelling
Fevere

Systemic problems

Xray: joint effusion

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18
Q

Osteoporosis

A

Osteopenia: reduced bone mass but ratio of bone mineral to matrix is normal

Poor diet
Low oestrogen

Normal levels of calcium, phosphat, PTH and ALP

Treat with bisphosphonates

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19
Q

Osteomalacia

A

Decreased bone mineralisation so low mineral to matrix ratio

Insufficient Ca2+ due to low Vitamin D or increased phosphate loss in kidneys

Ca2+ low
Vitamin D low

Phosphate high
ALP high

Diffuse pain particularly femur, pelvis and spine
Bone bowing and difficulty walking

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20
Q

What is Hammer toe?

A

Flexion and PIJ and Extension at DIJ in 2nd 3rd 4th toes

Can be rigid or flexible

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21
Q

Supracondylar humeral fractures

A

Damage

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22
Q

What is Compartment syndrome?

A

Pressure build up in a closed space (compartment) causing severe pain

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23
Q

What causes Compartment Syndrome?

A

Fluid in the compartment

  • Blood in trauma
  • Pus in infection

Trauma- long bone especially

  • Fractures
  • Crush
  • Haematoma
Burns
Infection
Prolonged compression
Muscle hypertrophy e.g. athletes
Severe ascites
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24
Q

How does Compartment syndrome present?

A

Early:

  • Burning, deep and aching PAIN, builds as pressure increases
  • Worsened by passive stretching of muscles
  • Paraesthesia
  • Swelling of compartment
Late:
- Loss of distal Pulses  (cap refill reduced)
- Ischaemia: rest of 6 Ps
Pallor 
Paralysis
Perishingly cold
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25
Q

Where are the common sites for Compartment syndrome?

A

MC: Lower limb

Also
Forearm
Gluteal-sciatic nerve palsy
Abdomen: major organ injury

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26
Q

How is Compartment Syndrome investigated?

A

Intracompartmental pressure measurements​

Wick catheters, pressure transducers, needle manometry, etc.​

(Nasogastric tube can be used in abdominal compartment syndrome​)

MRI may help in ambiguous cases​

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27
Q

How is Compartment Syndrome managed?

A

urgent decompression to prevent ischaemia

  • Remove casts/bandage
  • Elevate the limb

Fasciotomy-skin and deep fascia are cut along length of compartment and left open until pressure is releived
Abx, analgesia, phsio after

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28
Q

What are the complications of Compartment Syndrome?

A

Tissue necrosis. In muscles this leads to fibrosis, shorteining, ischaemic contracture and reduced function

29
Q

What structures may be affected in Anterior Lower Leg Compartment Syndrome?

A

Deep fibular Nerve

Anterior Tibial Artery

30
Q

What structures may be affected in Superficial Posterior Lower Leg Compartment Syndrome?

A

Tibial nerve

31
Q

What structures may be affected in Deep Posterior Lower Leg Compartment Syndrome?

A

Tibial nerve and vessels

Fibualr artery

32
Q

What structures may be affected in Later Lower Leg Compartment Syndrome?

A

Deep and Superficial fibular nerves

33
Q

What structures may be affected in Anterior (ventral) forearm Syndrome?

A

Median and ulnar nerves

Radial and ulnar arteries

34
Q

What structures may be affected in Posterior (dorsal) forearm Compartment Syndrome?

A

Posterior Interosseus nerve (deep branch of radial)

35
Q

What is Osteomyelitis?

A

Infection of bone marrow leading to bone destruction and necrosis

It can spread to cortex and periosteum (causes necrosis) via the Haversian canals

36
Q

What are the causative organsims in Osteomyelitis?

A

Staph Aureus

H. Influenzae

Streps

Ceftreiaxone or penicillins
Vancomycin for MRSA

37
Q

What are the risk factors for Osteomyelitis?

A

Trauma​

  • Open fracture​
  • Surgery​

Prosthetics – more likely to become infected as bacteria can easily form a biofilm​

Diabetes → ulcer formation → infection spread to exposed bone​

IV drug abuse​

Immunosuppression​

Chronic steroid use​

Tuberculosis​

Sickle-cell anaemia

38
Q

How does Osteomyelitis present?

A
Fever
Tenderness over bone
Imobility 
Pain, redness and swelling
Joint pain when associated with Septic Arthritis 

Back pain, worse at rest and nerve patterns of pain when in spine

39
Q

What are the investigations for Osteomyelitis?

A

Bloods
MRI
Biopsy is definitive

XRAY:

  • periosteal reaction and necrosis ~1 week later
  • sequestrum-dead bone isolated from live bone by necrosis looks like a white circle with black ring
  • involucrum:new layer of normal bone growth from periosteum
40
Q

What are the depths of Osteomyelitis?

A

Medullary

Superficial – Localised to one area of cortex​

Localised – Cortex breached, medulla infiltrated​

Diffuse – Cortex breached, medulla infiltrated, cortex on the OTHER SIDE also breached

41
Q

How is Osteomyelitis managed?

A

Depride and saline washout

Remove prosthesis

Bone graft or antibiotic implants

6 weeks of antibiotics

Hyperbaric O2 therapy if recurrent

42
Q

What is Septic Arthritis?

A

invasion of a joint by an infectious agent resulting in joint inflammation

Most often in hip or knee

Pus in joints will erode the cartialge

43
Q

How does Septic Arthritis present?

A
Rubor
Tumor
Calor
Dolor
Loss of function
ESPECIALLY IF SYSTEMICALLY UNWELL
44
Q

What are the causative organisms of Septic Arthritis?

A

Staph Aureus- Flucloxacillin or Clindamycin

MRSA-Vancomycin

May enter via Inocculation (directly) or blood stream

45
Q

What are the risk factors for Septic Arthritis?

A

RA or OA

Joint prosthesis​

Low socioeconomic status​

IV drug abuse​

Alcoholism​

Diabetes​

Puncture wound to the joint​

  • Traumatic​
  • Iatrogenic from surgery or injections such as steroids for arthritis relief​

Cutaneous Ulcers

46
Q

How is Septic Arthritis investigated?

A

Bloods
Synovial aspiration: gram stain and culture and check for Gout
MRSA swabs
MRI will show inflammation

47
Q

How is Septic Arthritis manged?

A

Abx immediately
Surgical washout-2 incisions, one pump saline in other suck it out
Flush until all pus has gone

48
Q

What is Kocher’s criteria?

A
Suspecting SA in children:
NEWT
Non weight bearing
ESR >40, CRP >20
WCC >12
Temperatur >38.5

1 feature = 3%
2 = 40%
3 = 93%
4 = 99%

49
Q

What are Newman’s 4 points?

A

Suspecting Septic Arthritis:

  • Pathogen isolated from joint
  • Pathogen isolated from blood in context of hot red joint
  • Typical features and turbid joint fluid in context of previous Abx
  • Post mortem
50
Q

What is Paget’s disease of the bone?

A

Chronic excessive breakdown and formation of bone due to increased osteoclast and blast action which leads to remodelling

There is more bone but it is non-lamellar and so weaker

51
Q

What causes Paget’s disease?

A

Genetic-AD

Viral

52
Q

How does Paget’s disease present?

A

Often asymptomatic

RAISED ALP

Pathological fractures

  • Non-mechanical bone pain
  • Bone deformity
  • Riased skin temp
53
Q

Which bones are often affected by Paget’s disease?

A

Axial skeleton

Long bones and skull most often affected:

  • Pelvis
  • Lumbar spine
  • Femur
  • Tibia
  • Skull
54
Q

What are the complications of Paget’s disease?

A
  • Increased risk of pathological fractures as weaker and highly vascular so risk of bleeding
55
Q

What are the complications of Paget’s disease?

A

Increased risk of pathological fractures as weaker and highly vascular so risk of bleeding and increased TPR which can lead to heart failure

Bone deformities:

  • Spine curvatures: hypohosis and spinal stenosis/nerve compression such as sciatica or Corda Equina
  • Tibia bowing
  • Frontal bossing of skull and increased head size: may cause deafness and tinnitus due to CN8 compression and/or ear ossicle remodelling
  • Enlarged maxilla

Osteoarthritis if near a joint

56
Q

How is Paget’s disease investigated?

A

Bone-specific ALP
(maybe raised caclium and phosphate)

X-ray:

  • Osteolysis (lucency)
  • Lots of bone
  • V shape between healthy and diseased bone
  • Cotton wool on skull

May biopsy to rule out malignancy

57
Q

How is Paget’s disease managed?

A
Analgesia
Monitor for osteosarcoma
Walking aides
Bisphosphonates
Relieve nerve compression
ALENDRONATE to reduce pain and deformity
58
Q

What are the causes of pathological fractures?

A

Atypical locations or very low trauma

  • Osteoporosis
  • Osteomalacia
  • Bone cancers and tumours
  • Bone cysts
  • Paget’s disease
59
Q

What are the causes of pathological fractures?

A

Atypical locations or very low trauma

  • Osteoporosis
  • Osteomalacia
  • Bone cancers and tumours
  • Bone cysts
  • Paget’s disease
60
Q

How can Myeloma be detected?

A

Bence-Jones proteins

61
Q

How are bone-cancers managed?

A

Debarking: removal of metaplastic soft tissue from around bone

Chemo and radio

Replace joint if near joint

Prophylactic fixation: Mirel’s scoring system

Bisphosphonates reduce weakening

62
Q

What antibiotics are used prohpylactically in surgeru?

A

Leicester uses 1.2g of co-amoxiclav on induction followed by 600mg over 8 hours post-op and then 600mg over 16 hours post-op

Teicoplanin is easier-one dose on induction

Swab for MRSA

63
Q

What antibiotics are given for Open Fractures?

A

1.2g co-amoxiclav on A&E presentation

Or clandamycin/cefuroxamime

64
Q

What are the antibiotics given for Bite Wounds?

A

Debride and leave in sterile dressing rather than close

Tetanus risk

Swab the wound

Dog Bites: Pasturella, strep, staph and Neisseria
Cat Bites:
Human bites:

Give co-amoxiclav 5 days OR doxycycline + metronidazole if penicllin allergic

65
Q

What are the antibiotics given for Bite Wounds?

A

Debride and leave in sterile dressing rather than close

Tetanus risk

Swab the wound

Dog Bites: Pasturella, strep, staph and Neisseria
Cat Bites: Pasturella, strep, Neisseria
Human bites:

Give co-amoxiclav 5 days OR doxycycline + metronidazole if penicllin allergic

66
Q

How are open fractures treated?

A

BOAST

  • IV antibiotics within 3 hours of injury and continued until debridement
    1. 2g co-amoxiclav or 1.5 cefuroxime
    1. 2 g co-amoxiclav 1.5mg/kg from debirdement and 72 hours after/closure of wound
  • Assess neurovascular status (vascular damage and compartment syndrome require immediate surgery)
  • Splint limb
67
Q

What types of joint surgeries are there?

A

Replacement: give function back

Fusion: prevent further pain where replacements are not usually sucessful e.g. ankle

Removal: e.g. toe joints or trapezium in OA

68
Q

CAUSES OF A SWOLLEN JOINT

A

CHRIST

Crystal arthropathies
Haemophilia
Rheumatoid arthritis (and other inflammatory)
Infection
Synovial pathology
Trauma