Patho of Osteo, Paget and more Flashcards

1
Q

Define osteopenia

A

Radiographically bone mass 1 to 2.5 standard deviasions below meak PEAK bone mass

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2
Q

Define osteoporosis

A

radiographically bone mass at least 2.5 standard deviations below mean peak bone mass
presence of atraumatic vertebral compression
localized disuse osteoporosis
generalized primary and secondary to a variety of conditions

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3
Q

Key forms of osteoporosis

A

Idiopathic
Postmenopausal
Senile

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4
Q

Define senile osteoporosis

A

bone density is reduced due to aging

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5
Q

define postmenopausal osteoporosis

A

bone density reduced due to lack of estrogen
decreased estrogen actually increases both bone resoption and formation - formation cannot keep up with resorption, net loss of bone
most bone loss within 5 years of onset

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6
Q

Fators effecting bone mass

A
Age: F>50 M>70
F>M
Asian, White, Hispanic
genetics
gonadal steroids
growth hormone
timing of puberty
calcium intake
exercise
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7
Q

Key genetic factors for osteoporosis

A

Bone hoemeostasis pathway LRP5
RANKL, OPG, RANK
HLA locus unfluencing inflammation and calcium metabolism
varieant in Vit D receptor and signalling

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8
Q

Clinical manifestations of osteoporosis

A

Silent disease - loss without symptoms
present with bone pain and fracture in weight-bearing area
vertebral fractures in thoracic and lumbar
complications from fractures of femoral neck, pelvis, or spine

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9
Q

Detection of osteooporosis

A

Blood levels of calcium, phosphorus, PTH and alkaline phosphatase are normal
Eual-Energy X-ray Absorption scan (DEXA) wwith quatitiative computed tomography to measure bone density

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10
Q

Prevention of osteoprorsis

A

Starts in young adults
can regain density with:
wight-bearing exercises,
dietary Vit D and calcium (decrease with caffeine, alcohol, and smoking),
medicines to treat and prevent bone loss

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11
Q

Osteoporosis amenorrhea

A

Absence of regular menstrual cycle for three months or longer
3% young female
due to premature ovarian failure, excessive exercise, athletes, eating disorders, pituitary gland tumors.
Negatively affect peak bone mass and increase risk of osteoporosis

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12
Q

Paget’s disease overview

A

Disease of increased but organized and structurally unsound bone mass) clast and blast imbalance)
Etiology unknown: genetic link with 40% having it in the family. Environmental show signs of Paramyxoviridae within clasts. Measels and respiratory syncytial virus

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13
Q

Paget disease 3 phases

A
  1. osteolytic stage - uncontrolled osteoclast activity
  2. mixed osteoclast-blast stage - osteoblasts try to catch up
  3. Burn out quiescent osteoclastic stage - clasts burn out, osteoblasts continue to make bone but no remodeling by osteoclasts
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14
Q

Paget’s disease demographics

A

Late adulthood (>50)
M>F
3% of autopsies
More in people of English decent. Nonexistent in Scandanavia, Asia, Africa, and south Africa

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15
Q

Paget’s disease clinical manifestations

A

enlarged head - hat doesn’t fit
deafness
increased limb volume
increased warmth over bone

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16
Q

Paget’s disease lab results

A

Increased alkaline phosphatase due to osteoblast activity
Increased Urinary hydroxyproline due to collogen destruction
(Calcium, phosphate, PTH all normal)

17
Q

Paget’s disease other symptoms

A

Fatigue
increased hat size
bone pain and deformity
pathological fracture
osteoarthritis secondary to bone deformity
nerve compression leading to deafness or blindness
increased risk of osteosarcoma (3x)

18
Q

Paget’s disease recurrence

A

1/3 bone scan
1/3 biomarkers (increased ALP and urine hydroxyproline)
1/3 both

19
Q

Rickets age and determining factors

A

children

deranged bone growth

20
Q

Osteomalacia

A

Adults
remodeled bone is inadequately mineralized
osteopenia and factures

21
Q

Vitamin D deficiency

A

Decreased sun exposure
poor diet
malabsorption
liver and renal failure

22
Q

Rickets disease histological findings

A

palisades of cartilage are lost

23
Q

Ricket’s presentation

A
Low vit D in children
Pigeon breast deformity
frontal bossing
rachitic rosary
craniotabes
lumbar lordosis
24
Q

Ostoemalacia presentation

A

Low vit d in adults
increased fractures due to weak bones
inadequate mineralization of osteoid in remodeled bone (weight-bearing bones in the vertebra and hips_)
abnormal labs: decreased serum calcium and phosphate. Increased PTH. Elevated alk phos

25
Osteomalacia histology
Trabecular bone covered in excessive amounts of osteoid
26
Parathyroid hormone role in bone formation
increased RANKL expression in osteoblasts leading to osteoclast activation and calcium mobilization increase resorption of calcium by renal tubules increased urinary excretion of phosphates increased synthesis of active vit d net elevation of serum calcium should inhibit PTH production
27
Hyperthyrodism and bone changes
Excessive or inappropriate levels of PTH Stones, bones, moans, and groans entire skeleton affected fractures, bone deformation, joint problems
28
Hyperparathyroidism and bone morphology
osteoporosis brown tumors - microfractures and secondary hemorrhages, influx of macrophages, reparative fibrous tissue osteitis fibrosa cystica - combination bone cell activity, cystic brown tumors, peritrabecular fibrosis, severe hyperparathyroidism, rarely encountered now
29
Renal osteodystrophy
Skeletal changes in chronic renal disease 1. osteopenia/porosis 2. osteomalacia 3. secondary hyperparathyroidism 4. growth retardation
30
Renal osteodystrophy types
1. high-turnover - increased bone resorption and bone formation with former predomination 2. Low-turnover or aplastic disease - adynamic bone due to decreased osteoblast and clast activity 3. Mixed pattern - areas of high turnover and areas of low turnover