MSK Flashcards

(28 cards)

1
Q

what is transient synovitis

A

acute hip pain following a recent viral infection
typical age 3-8 years

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2
Q

features of transient synovitis

A

limp/refusal to weight bear
groin or hip pain
low grade fever

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3
Q

management of transient synovitis

A

rest and analgesia
refer if child has fever

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4
Q

what is perthes’ disease

A

degenerative condition due to AVN of the femoral head

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5
Q

who commonly gets perthes disease

A

more common in boys
typically 4-8 years old

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6
Q

features of perthes disease

A

hip pain: develops over a few weeks
limp
stiffness and reduced range of hip movement
x-ray: early changes- widening of joint space. later changes- decreased femoral head size/flattening

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7
Q

diagnosis of perthes disease

A

plain x-ray
technetium bone scan or MRI if normal x-ray

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8
Q

complications of perthes disease

A

osteoarthritis
premature fusion of the growth plates

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9
Q

staging for perthes

A

catterall staging

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10
Q

management of perthes

A

keep femoral head within the acetabulum: cast, brace
less than 6 years: observation
older: surgical management with moderate results

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11
Q

general management in GP of child < 3 with acute limp

A

urgent specialist assessment

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12
Q

typical age of SUFE

A

10-15 years

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13
Q

features of SUFE

A

hip, groin, medial thigh or knee pain
loss of internal rotation of the leg in flexion
bilateral in 20%

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14
Q

investigations for SUFE

A

AP and lateral views are diagnostic

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15
Q

management of SUFE

A

internal fixation

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16
Q

describe talipes equinovarus

A

inverted and plantar flexed foot

17
Q

associations with talipes equinovarus

A

spina bifida
cerebral palsy
edwards syndrome
oligohydramnios
arthrogryposis

18
Q

management of talipes equinovarus

A

ponseti method

19
Q

predisposing factors for rickets

A

dietary deficiency of calcium
prolonged breastfeeding
unsupplemented cows milk
lack of sunlight

20
Q

features of rickets

A

aching bones and joints
lower limb abnormalities (bow legs, knock knees)
rickety rosary- swelling at the costochondral junction
kyphoscoliosis
craniotabes (soft skull)
harrison’s sulcus

21
Q

investigations for rickets

A

low vit D levels
reduced serum calcium
raised ALP

22
Q

management of rickets

23
Q

what is achondroplasia

A

autosomal dominant disorder associated with short stature
mutation in fibroblast growth factor receptor 3 gene

24
Q

features of achondroplasia

A

short limbs with shortened fingers
large head with frontal bossing and narrow foramen magnum
midface hypoplasia with flattened nasal bridge

25
management of osgood schlatter disease
supportive
26
what is oteogenesis imperfecta
group of disorders of collagen metabolism resulting in bone fragility and fractures
27
inheritance of osteogenesis imperfecta
autosomal dominant
28
presentation of osteogenesis imperfecta
presents in childhood fractures following minor trauma blue sclera deafness secondary to otosclerosis dental imperfections