Bone Pathology Flashcards

1
Q

What hormones are typically involved in bone remodelling?

A

parathyroid hormone
vitamin D3
oestrogen

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2
Q

special tests that can be done to assess bone biochemistry

A

blood calcium
osteoblast activity
- serum alkaline phosphate
- osteocalcin

osteoclast activity
- collagen degradation urine and blood

parathyroid hormone

vitamin D assays

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3
Q

osteogenesis imperfecta features

A

aka “brittle bone disease”
type 1 collagen defect
inheritance varies - 4 main types
- sometimes associated with dentinogenesis imperfecta

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4
Q

achondroplasia features

A

autosomal dominant
poor endochonral ossification
dwarfism

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5
Q

osteopetrosis features

A

“marble bone disease”
lack of osteoclast activity
failure of resorption and marrow obliteration

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6
Q

osteoporosis complications

A

cranial nerve compression. bone fractures, dental impaction etc

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7
Q

fibrous dysplasia features

A

uncommon
- gene defects
leads to fibrous replacement of bone
- slow growing, asymptomatic bony swelling
active under 20 years
- stop growing after active growth period
serum biochemistry normal

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8
Q

clinical phenotypes of fibrous dysplasia

A

monostotic
- single bone
- more common
- maxilla > mandible
- facial symmetry

polostotic
- many bones

can be syndromic
- albrights syndrome

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9
Q

what is rarefying osteitis?

A

localised loss of bone in response to inflammation

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10
Q

what is condensing osteitis?

A

localised increase in bone density in response to low-grade inflammation
- periapical radiopacity, often poorly defined
- may eventually lead to external root resorption if chronic

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11
Q

idiopathic osetosclerosis

A

localised increase in bone density of unknown cause
- always asymptomatic
- no bony expansion
- no effect on adjacent teeth or structures
- most common in premoaler-molar region of mandible

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12
Q

Alveolar osteitis risk factors

A

lower extraction
complex extraction
women
smoking
rinsing too soon
posterior teeth

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13
Q

dry socket signs

A

severe pain, loss of clot, blood sequestra

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14
Q

osteomyelitis

A

rare endogenous infection acute or chronic
- suppuration is rare

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15
Q

bone necrosis - aetiology

A

osteomyelitis
avascular necrosis
-age-related ischaemia
- anti-resorptive medication
irradiation
- ORN - prone to infection

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16
Q

Anti resorptive drugs - how do they work?

A

inhibit osteoclasts
- used for osteoporosis, Bone metastases, Paget’s

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17
Q

what is osteoporosis?

A

bone atrophy
- resorption exceeds formation
- quantitative deficiency

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18
Q

osteoporosis clinical features

A

symtomless (until bone broken)
weak bone
antrum enlarged

19
Q

radiographic features of osteoporosis

A

loss of normal bone markings

20
Q

osteoporosis risk factors

A

sex hormone status
age
calcium status and physical activity
secondary
- bushings
hyperparathyroidism
diabetes mellitus

21
Q

Rickets and osteomalacia - cause

A

vitamin d deficiency
osteoid forms but fails to calcify

22
Q

Vitamin D deficiency cause

A

lack of sunlight
diet
malabsorption
renal causes

23
Q

rickets leads to…

A

low calcium
poor endochondral bone
raised alkaline phosphate

24
Q

what is hyperparathyroidism

A

calcium mobilised from bones
- generalised osteoporosis
- metastatic calcification e.g. kidneys

25
Q

types of hyperparathyroidism

A

primary
- neoplasia or hyperplasie
secondary
- hypocalcaemia - vitamin D deficiency
tertiary
- hyperplasia as a result of prolonged secondary

26
Q

primary hyperparathydrodism prevalence

A

1:1000
mainly postmenopausal women
F:M 3:1

27
Q

primary hyperparathyroidism most common aetiology

A

90% caused due to parathyroid adenoma
- increase parathyroid hormone
- hypercalcaemia
- increased bone turnover

28
Q

cherubim features

A

rare condition
autosomal dominant inheritance
grow before about 7 years and regress after puberty
multilocular leisons in multiple quadrants

29
Q

cherubism histology

A

vascular giant cell lesions

30
Q

Paget’s disease of bone - epidemiology

A

age>40
M>F
3% of routine autopsy

31
Q

Paget’s disease clinical signs

A

bony swelling, pain, nerve compression

32
Q

Paget’s disease aetiology

A

racal predilection
serum biochemistry
- raised alkaline phosphatase

33
Q

Paget’s disease bone pattern

A

variable
changes as disease progresses
- osteoporotic
- mixed
- osteosclerotic

34
Q

Paget’s disease dental changes

A

loss of lamina dura
hypercementosis
migration
- due to bone enlargement

35
Q

Paget’s complications

A

infection
bone tumours

36
Q

Paget’s histology

A

increased bone turnover
osteoclastic and osteoblastic activity
will burn out

37
Q

what is an osteoma?

A

a benign tumour of bone
solitary
mostly cortical bone
slow growing

38
Q

Multiple osteomas may indicate…

A

Gardner syndrome
- associated with multiple GI polyps

39
Q

osteoblastoma features

A

rare
often very active growth

40
Q

Osteoporosis clinical features

A

symptomless
weak bone
antrum enlarged

41
Q

osteoporosis radiographic features

A

loss of normal bone markings

42
Q

give examples of cementum lesions

A

cementoblastoma
cemento-osseous dysplasias

43
Q

What is a cementoblastoma?

A

a neoplasm attached to the root
histology same as osteoblastoma