biochemistry Flashcards

1
Q

what is osteochondritis dissecans?

A

inflammation of bone and cartilage

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2
Q

who does osteochondritis dissecans usually occur in and why?

A

young adults
increased physical activity and body weight

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3
Q

what does recurrent impact trauma lead to?

A

bleeding + oedema in bone -> capillary compression -> bone necrosis -> bone fragmentation

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4
Q

how does osteochondritis dissecans usually present?

A

poorly localised pain
effusion
locking

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5
Q

what is the management of osteochondritis dissecans?

A

pinning or removal or unstable fragments

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6
Q

what is avascular necrosis?

A

ischaemic necrosis of bone (common at hip)

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7
Q

what is avascular necrosis due to?

A

fractures disrupting blood supply
alcohol
steroid abuse
SLE

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8
Q

how can necrosis lead to OA?

A

necrosis -> patchy sclerosis -> subchondral collapse + irregular articular surface -> OA

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9
Q

what is osteoporosis?

A

fragile bone due to reduced bone mineral density -> fractures

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10
Q

what are the risk factors of osteoporosis?

A

lack of exercise
poor diet
lack of sunlight

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11
Q

when does osteoporosis usually occur?

A

post-menopause
old age
steroid/alcohol use
malnutrition

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12
Q

what is the diagnostic test for osteoporosis?

A

DEXA scan

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13
Q

what is the management of osteoporosis?

A

prevent fractures - lifestyle + strengthen + vitD/Ca2+ supplements

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14
Q

what is the treatment for slow deteriorating osteoporosis?

A

bisphosphonates -> reduce osteoclast activity
teriparatide -> synthetic PTH -> stimulates osteoclasts

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15
Q

what is osteomalacia and Rickett’s?

A

abnormal softening of bone due to deficient mineralisation

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16
Q

what is osteomalacia and Rickett’s due to?

A

insufficient calcium absorption
less dietary calcium/vitD deficiency/less phosphate (inc. renal losses)

17
Q

how does osteomalacia and Rickett’s present?

A

bone pain
soft bone deformities fractures
hypocalcaemia signs

18
Q

what is a physical sign of Rickett’s?

A

bowing of the legs

19
Q

what will be seen in investigations in osteomalacia and Rickett’s?

A

low calcium
low serum phosphate
high serum ALP

20
Q

what is the management of osteomalacia and Rickett’s?

A

vitD + calcium + phosphate supplementation

21
Q

what is Paget’s disease?

A

thickened brittle and misshapen bones

22
Q

what causes Paget’s disease?

A

osteoclasts/osteoblasts speeding up

23
Q

what are the stages of Paget’s disease?

A

lytic phase -> mixed -> sclerotic phase

24
Q

who does Paget’s disease usually affect and where?

A

older patients
pelvis
spine
skull
femur

25
Q

how does Paget’s disease usually present?

A

constant dull bone pain

26
Q

what will be seen in investigations?

A

raised ALP
normal calcium + phosphorus

27
Q

what investigation is used in Paget’s disease?

28
Q

what is the management of Paget’s disease?

A

bisphosphonates (calcitonin if excessive)