DSA22 Bone Pain (Osteoporosis, Osteomalacia, Rickets, and Paget Disease)

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39 Terms

1
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Osteoporosis is characterized by

loss of bone density leading to decreased bone strength/increased susceptibility to fractures

<p>loss of bone <strong>density </strong>leading to decreased bone strength/increased susceptibility to fractures</p>
2
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osteomalacia vs rickets

osteomalacia: defective mineralization of osteoid

rickets: defective mineralization of cartilage in the epiphyseal growth plates (so this can only happen in children)

3
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can osteomalacia and rickets occur simultaneously?

yes, but in kids (only osteomalacia in adults)

4
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How does vitamin D affect bone turnover?

Helps mineralize osteoid by:
- Increasing serum calcium,
- Increasing serum phosphate

<p>Helps mineralize osteoid by: <br>- Increasing serum calcium, <br>- Increasing serum phosphate</p>
5
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without vitamin D, calcium may be normal due to _______ action, but bone mineralization is still impaired due to low _______

PTH
low phosphate

<p>PTH<br>low phosphate</p>
6
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RANK/RANKL function

Binding of RANKL to RANK regulates osteoclast differentiation and activation --> bone reabsorption

<p>Binding of RANKL to RANK regulates osteoclast differentiation and activation --&gt; bone reabsorption</p>
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RANK/RANKL is inhibited by ______

OPG

<p>OPG</p>
8
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Osteopenia= bone mass _______ standard deviations below the mean

1-1.25

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Osteoporosis= bone mass _____ standard deviations below the mean, significantly increases the risk of ________

2.5
fracture

10
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how does estrogen deficiency play a major role in osteoporosis?

leads to increased bone resorption and formation, but the resorption wins out (high-turnover osteoporosis)

11
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how does reduced physical exercise play a role in osteoporosis?

mechanical force stimulates bone remodeling --> less weight-bearing exercise contributes to decreased bone density

12
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what is senile osteoporosis?

gradual loss of bone mass as pts age (esp over 70 years old)

- osteoblasts activity reduced with age

(low turnover osteoporosis)

13
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In osteoporosis, the ________ are thinner leading to increased __________ and eventual collapse

trabeculae
microfracture

<p>trabeculae<br>microfracture</p>
14
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When you think about osteomalacia and rickets, think defective ___________ due to vitamin D deficiency

mineralization

15
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breastfed infants need to supplement w/ ________ due to significant risk for ________

vitamin D
rickets

16
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Rickets is characterized by a defect in mineralization and the widening of the __________

epiphyseal plates

<p>epiphyseal plates</p>
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osteomalacia is a defects in the mineralization of the _________

bone matrix

<p>bone matrix</p>
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What is the most important lab marker in the diagnosis of rickets?

- increased alkaline phosphatase (ALP)

19
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osteomalacia histology

more osteoid (orange) around the bone (green) which has accumulated bc it is not properly mineralized

<p>more osteoid (orange) around the bone (green) which has accumulated bc it is not properly mineralized</p>
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In osteomalacia, the bone is weak and vulnerable to gross fractures or microfractures, which are most likely to affect __________ and __________

vertebral bodies and femoral necks

21
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rickets clinical features

- craniotabes (soft skull)

- frontal bossing

- "rachitic rosary" (chest deformity)

- bowed legs, lumbar lordosis

<p>- craniotabes (soft skull)</p><p>- frontal bossing</p><p>- <strong>"rachitic rosary"</strong> (chest deformity)</p><p>- bowed legs, lumbar lordosis</p>
22
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rickets histology

- Normal (L): costochondral junction of a young child illustrates formation of cartilage pallisades and orderly transition from cartilage to new bone

- Rickets (R): Detail of rachitic costochondral junction in which the palisades of cartilage is lost; darker trabeculae are well-formed bone; paler trabeculae consist of uncalcified osteoid

<p>- Normal (L): costochondral junction of a young child illustrates formation of cartilage pallisades and orderly transition from cartilage to new bone</p><p>- Rickets (R): Detail of rachitic costochondral junction in which the <strong>palisades of cartilage is lost</strong>; darker trabeculae are well-formed bone; paler trabeculae consist of uncalcified osteoid</p>
23
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primary hyperparathyroidism

hypercalcemia results from abnormally active parathyroid glands

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Secondary hyperparathyroidism

hypocalcemia leads to reactive overproduction of PTH

25
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Primary hyperparathyroidism is usually due to...

a parathyroid adenoma

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secondary hyperparathyroidism is usually due to...

renal disease

27
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In secondary hyperparathyroidism, chronic renal disease commonly leads to ________ due to inability of the kidney to make active _______ which impairs _____ absorption

In secondary hyperparathyroidism, chronic renal disease commonly leads to hypocalcemia due to inability of the kidney to make active vit D which impairs Ca absorption

28
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renal osteodystrophy

Bone lesions due to secondary hyperparathyroidism due to chronic renal disease (hypocalcemia --> increased PTH)

29
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x-ray findings in hyperparathyroidism

subperiostal resorption typically seen at radial aspect of the middle phalanx of the index and middle fingers

<p><strong>subperiostal resorption</strong> typically seen at radial aspect of the middle phalanx of the index and middle fingers</p>
30
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dissecting osteitis is associated with...

hyperparathyroidism

(I think this is just a word for lots of osteoclast activity?)

<p>hyperparathyroidism <br><br>(I think this is just a word for lots of osteoclast activity?)</p>
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What are brown tumors?

lytic lesions due to high PTH levels (brown due to hemorrhage)

<p>lytic lesions due to high PTH levels (brown due to hemorrhage)</p>
32
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brown tumors are more likely to occur in primary or secondary hyperparathyroidism?

primary hyperparathyroidism

33
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What is Paget's disease?

chronic metabolic disorder characterized by increased bone turnover and breakdown secondary to excessive and disorganized osteoclastic and osteoblastic activity

34
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Hallmark of Paget's Disease

mix of osteolytic and osteoblastic phases

<p>mix of osteolytic and osteoblastic phases</p>
35
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Paget's disease histology

The "mosaic" pattern outlines irregular patches of sclerotic lamellar bone reflecting previous waves of bone resorption and reformation.

<p>The "mosaic" pattern outlines irregular patches of sclerotic lamellar bone reflecting previous waves of bone resorption and reformation.</p>
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Paget's disease labs

- Increase alkaline Phospahatase
- normal Ca
- normal Phos

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What is a feared complication of long-standing Paget's disease?

osteosarcoma

38
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Paget's disease facial clinical features

- enlargement of craniofacial skeleton (may produce leontiasis ossea (lion face))

<p>- enlargement of craniofacial skeleton (may produce leontiasis ossea (lion face))</p>
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Pagets disease predominantly involves the __________ and __________

axial skeleton and femur