2. Histopathology and radiology Flashcards

1
Q

What are the 2 broad categorisations of mature bone?

A

Cortical

Cancellous

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2
Q

What % of bone is cortical and where is cortical bone most abundant?

A

80% of bone

Long bones

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3
Q

Describe the structure of cortical bone

A

Mature, lamellar bone - PARALLEL lamellae

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4
Q

Describe the structure of cancellous bone

A

Mature, lamellar bone - CONCENTRIC lamellae

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5
Q

What is the primary function of cancellous bone and where is it most abundant?

A

Metabolic fx - can dissolve/ resorb quickly for Ca++ homeostasis
Vertebrae and pelvis

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6
Q

Describe the process of mineralisation

A

Process through which an organic substance becomes impregnated by inorganic substances

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7
Q

What name is given to immature bone? Describe it structure

A

Woven bone

Irregularly-arranged collagen

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8
Q

What are the cannaliculae in bone?

A

Communication channels for osteocytes

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9
Q

What can be seen where there is osteoclast activity?

A

Howship’s lacunae

= “bite-marks” where breakdown is occuring

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10
Q

Recall the relative proportions of organic and inorganic matter in bone, and summarise the composition of each of these

A

Organic (cells and protein matrix) = 35%

Inorganic (Ca hydroxyapatite) = 65%

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11
Q

What is the role of the RANK ligand in bone homeostasis?

A

When RANK combines with RANK-L osteoclasts are stimulated to differentiate

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12
Q

By what mechanism is osteoclast action inhibited?

A

Osteoprotegerin

Inhibitor of RANK:RANK-L binding

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13
Q

Where are osteocytes located in bone?

A

Lacunae

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14
Q

Distinguish between primary and secondary osteoperosis

A
Primary = age-related, post-menopause
Secondary = caused by drugs (eg thyroid drugs) or systemic disease
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15
Q

Recall the key distinguishing features of osteoperosis from other metabolic bone diseases

A

NORMAL mineralisation so serum biochemistry is normal - just a reduced mass of bone

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16
Q

What is raised ALP indicative of? Give 4 examples of where this might be seen

A

Increased bone turnover

  1. Paget’s
  2. Osteomalacia
  3. Bony Mets
  4. HyperPTHism
17
Q

Sumamrise the possible radiological findings in osteoperosis

A

MAY BE NORMAL
OR
1. Osteopaenic
2. Osteosclerotic

18
Q

Why might osteoperosis demonstrate osteopaenia

A

Loss of bone quantity rather than quality

19
Q

How does osteopaenia appear radiologically?

A

Reduced opacity

20
Q

What is osteosclerosis?

A

Increased bone density

21
Q

Recall 2 key features of osteomalacia radiologically

A
  1. Looser’s zone fractures (horizontal fracture in cortical bone)
  2. Codfish vertebrae
    (biconcave vertebrae)
22
Q

Recall 2 radiological features of Paget’s disease

A
  1. Cortical thickening

2. Coarsening trabeculae

23
Q

Describe how primary and secondary hyperPTHism can be distinguished radiologically?

A

Primary = bone resorption
Secondary = bone resorption AND INCREASED DENSITY
Bone resorption has appearance of erosion, and can lead to “brown tumour”

24
Q

What is renal osteodystrophy?

A
Comprises all the skeletal changes of CKS - a combo of:
OsteoMALACIA
OsteoSCLEROSIS
OsteoPEROSIS
OsteoTITIS FIBROSIS CYSTICA
25
Q

Describe the serum biochemistry of renal osteodystrophy (phosphate, calcium, PTH, pH)

A

HIGH phosphate
LOW calcium
HIGH PTH
Metabolic acidosis

26
Q

How does sclerosis appear radiologically?

A

Rugged vertebrae (Jersey spine)

27
Q

Recall 3 radiological features of renal osteodystrophy

A

Brown tumour
Jersey Spine
Soft tissue calcification around vessels

28
Q

Recall 2 radiological features of Rickets

A

Cupped and frayed metaphysis due to increased stress

Widenened unmineralised growth plate