Skel A-MEtabolic Bone Disease Flashcards

1
Q

Descriptive term for decreased bone or increased radiolucency of bone that occurs when bone resorption exceeds bone formation regardless of specific pathogenesis.

A

Osteopenia

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2
Q

What results when bone resorption exceeds bone formation regardless of specific pathogenesis?

A

Osteopenia

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3
Q

T/F: Radiographic findings of osteopenia does not alone allow a precise diagnosis

A

True

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4
Q

What are the four major causes of osteopenia?

A

Osteoporosis

Osteomalacia/ Rickets

Hyperparathyroidism

Neoplasm

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5
Q

Bone Cells:

Originates from the marrow stem cells, develop into osteoblasts

A

Osteoprogenitor cells

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6
Q

Bone cells:

Produces osteoid which is soft material main of 90-95% collagen and 5-10% ground substance, the mucopolysaccharide.

It is numerous in growing skeleton and decrease in number and size at maturity

A

OSTEOBLAST

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7
Q

Bone cell:

Arises from osteoblast that become entrapped in their own osteoid.

They maintain bone integrity

Mature bone cells

A

Osteocytes

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8
Q

Bone Cells:

Inactive/dormant osteoblast

A

Bone lining cells

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9
Q

Bone Cell:

Bone resorptive cells, derived from hematopoietic monocyte lineage.

Different lineage from other bone cells

A

Osteoclast

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10
Q

For normal bone density what is required

A

Osteoblastic=Osteoclastic activity

Normal nervous system function

Normal GI, Liver, Renal Function

Dietary intake of calcium and phosphorus

Normal endocrine function

Weight bearing exercises

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11
Q

Non-cellular constituents of bone:

% of wet weight of bone that is accounted for by water

A

20%

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12
Q

Non-cellular constituents of bone:

% of bone weight accounted for by cellular components

A

Tiny fraction

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13
Q

Non-cellular constituents of bone:

% of dry bone weight accounted for by organic matrix/osteoid

A

30%

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14
Q

Non-cellular constituents of bone:

% of dry bone weight accounted for by inorganic material

A

70%

Accounts for 70% of osseous tissue

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15
Q

Non-cellular constituents of bone:

Inorganic material exists as what ?

A

Calcium hydroxyapatite

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16
Q

Calcium homeostasis:

Function of the skeleton in calcium homeostasis

A

99% of calcium stored in skeleton

Serves as a reserve for serum calcium

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17
Q

Calcium homeostasis:

70% of plasma calcium is believed to be maintained how?

A

Continuous exchange of calcium ions between bone and extracellular fluid

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18
Q

Calcium homeostasis:

The remaining 30% of plasma calcium is mediated by what?

A

The function of Parathyroid hormone and Calcitonin

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19
Q

Osteoclast and Osteoblast function:

Osteoclast exist in pits on bone surfaced called?

A

Resorption bays or Howship’s Lacunae

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20
Q

Osteoclast and Osteoblast function:

Osteoclast function

A

Secretion of Collagenase to break down osteoid

Secrete Acid to break down calcium hydroxyapatite

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21
Q

Osteoclast and Osteoblast function:

What are substances that can have direct or indirect influence on osteoclasts increasing their function or numbers or both?

A

Parathyroid hormone

Active Vitamin D

Prostaglandin E2

Thyroid hormone

Heparin

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22
Q

Osteoclast and Osteoblast function:

Substance that inhibits osteoclast

A

Calcitonin

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23
Q

Metabolic bone disease:

Bone quantity not quality disorder

Associated with decreasing osteoblastic function with age

Estimated 30-50% loss before detectable radiographically

A

Osteoporosis

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24
Q

Metabolic bone disease:

Where is the predominant location of osteoporosis ?

A

Axial skeleton

Proximal long bones

*can be generalized of localized

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25
Metabolic bone disease: Senile Osteoporosis is (men/women) Post-menopausal osteoporosis is (men/women)
Senile-men PM- women
26
Metabolic bone disease: Inadequate mineralization of osteoid Related to deficiency in calcium, vitamin D or phosphorus which can be Deficiency caused by renal disease, sunlight deficiency, liver disease, dietary insufficiency and GI Disease
Osteomalacia
27
Metabolic bone disease: Primary type of HPT characterized by?
Increase PTH production usually benign adenoma
28
Metabolic bone disease: With Primary HPT you will see (hypercalcemia/hypocalcemia)
Hypercalcemia
29
Metabolic bone disease: Secondary HPT Characterized by?
Abnormal stimulation of glands by sustained hypocalcemia and hyperphosphatemia
30
Metabolic bone disease: Potential causes of secondary HPT
Renal disease GI Malabsorption
31
Metabolic bone disease: Tertiary HPT characterized by?
Long standing secondary HPT to the point parathyroid function is autonomous Can be related to ectopic tissue, or paraneoplastic syndrome
32
Metabolic bone disease: Function of PTH
Osteoclastic and osteocytic stimulation Osteoblastic inhibition Renal calcium absorption vs inhibition of phosphate resorption Renal stimulation of 1-Alpha- hydroxylase Indirection effect on GI absorption of calcium
33
Metabolic bone disease: Function of 1-alpha-hydroxylase
Increase formation of 1-25-vitamin D
34
Metabolic bone disease: Hormone? Secreted by the human parafollicular or C cells of the thyroid gland - Controlled by the serum calcium levels Inhibits bone calcium resorption by decreasing osteoclastic function and May lead to hypocalcemia and hypophosphatemia Inhibits GI calcium absorption Stimulates osteoblastic activity Inhibits renal tubular cell reabsorption of calcium
Calcitonin
35
Metabolic bone disease: MAjor causes of generalized osteoporosis
Age related Medication Endocrine Deficiency states Alcoholism Chronic liver disease Anemic state Osteogenesis imperfecta Idiopathic condition
36
Metabolic bone disease: Osteoporosis seen in - 1. Immobilization an disuse-fx healing 2. Complex region pain syndrome-sympathically mediation pain, Reflex sympathetic dystrophy syndrome 3. Transient regional osteoporosis
Regional osteoporosis
37
Metabolic bone disease: Describe CRPS/SMPS
Syndrome that typically follow trauma unilaterally Soft tissue swelling Very painful
38
Metabolic bone disease: Transient demineralization of the hip usually in healthy middle aged men, and pregnant women in 3rd trimester Affects left hip Acute pain & functional disability w/o previous trauma Clears up on its own-self limiting
Transient osteoporosis of the hip
39
Metabolic bone disease: Osteoporosis- 1. Discovered by Duncan et. al 2. Happens in 5-41% 3. Unpredictable 4. Affects joint nearest the disease
Regional migratory osteoporosis
40
Metabolic bone disease: 6 vertebral configurations in osteoporosis
Normal Losing horizontal trabeculation Anterior wedging Plana: ant/post collapse Bison cave endplates Angular endplate depression from fox
41
Metabolic bone disease: Plana vertebrae in osteoporosis may be caused by ?
Malignancies 1. Mets 2. Mult. Myeloma
42
Metabolic bone disease: Biconcave endplates in osteoporosis may be caused by?
Mult. Myeloma 5
43
Metabolic bone disease: Fx- Cause by Osteoporosis Low extremity bilaterally Pain major symptom Occurs when elastic strength < normal phys stress
Insufficiency Fox
44
Metabolic bone disease: Risk factors of osteoporosis ACCESS
Alcohol Corticosteroids Calcium low Estrogen low Smoking Sedentary lifestyle
45
Metabolic bone disease: Scan for bone density
Duel Energy X-ray Absorptiometry | DEXA/DXA
46
Metabolic bone disease: Associated with long term vitamin C deficiency Predominantly in children
Scurvy/Barlow’s disease- hypovitaminosis C
47
Metabolic bone disease: | What is the hallmark Scurvy?
Spontaneous bleeding due to capillary fragility SUBPERIOSTEAL BLEEDING —>BONE PAIN
48
Radiographic finding of Scurvy: dense zone of provisional mineralization- no secondary spongiosa
White line of frankel
49
Radiographic finding of Scurvy: Dense cortical margin of epiphysis with radiolucent center
Wimbergers ring
50
Radiographic finding of Scurvy: Irregular mataphyseal margin
Corner/angle sign
51
Radiographic finding of Scurvy: Bony protuberance at margin of ZPM Spurs
Pelken sign
52
Radiographic finding of Scurvy: Radiolucent metaphyseal band directly beneath ZPM, due to defective bone formation
Trumerfeld/subortic line | Leukemia lines in leukemia
53
Radiographic finding of Scurvy: Pathognomonic sign visible with healing
SUBPERIOSTEAL hemorrhage
54
Metabolic bone disease: Clinical findings of hypovitaminosis D
Muscle weakness Bone pain Deformities of pelvis, femur, tibia and spine
55
Radiographic features of osteomalacia: What are the radiographic features of osteomalacia ?
Osteopenia Coarse do trabecular pattern Loss of cortical definition Pseudo fx
56
Radiographic finding of osteomalacia: Deformities seen on radiograph
Weight bearing bones: 1. Triradiate pelvis 2. Acetabular protrusion 3. Femoral and tibial bowing 4. Kyphoscoliosis 5. Endplate concavity 6. Bell shaped thorax
57
Radiographic finding of osteomalacia: Common sight of osteomalacia
Femur Ribs Axillary border of scapula Pelvic rami
58
Radiographic finding of osteomalacia: AKA for pseudo fx
Umbauzonen/increment fx Looser’s lines Milkman syndrome Osteoid seams
59
Pseudo fx: Characterized by
Seam of unmineralized osteoid No trauma Perpendicular to cortex Ribs, pelvis, femur, no spine involvement Bone softening disease
60
Metabolic bone disease: Renal tubular loss of phosphorous, not cured by the administration of vitamin D
Resistant/refractory/ renal rickets
61
Metabolic bone disease: Secondary HPT + renal rickets =
Renal osteodystrophy
62
Clinical presentation of rickets
Muscle tetany irritability weakness delayed bone development small stature and bone deformities/bowing
63
T/F: findings of enlarged growth plates (trumpeting) and rib ends (rachitic rosary) are present in rickets
True
64
Metabolic bone disease: Generally an x-linked transmitted Renal tubular loss of phosphate Rickets develops In adults skeleton, develops osteosclerosis and enthesopathic paravertebral ligament Lumbar stenosis Type of dwarfism
Hypophosphatemia
65
Metabolic bone disease: Hypophosphatemia is classified under which group of syndromes?
Fanconi syndrome
66
Metabolic bone disease: Rare disease related to low serum alkaline phosphatase produced by osteoblasts Resembles rickets Radiolucent metaphyseal defect from physis to metaphysis
Hypophosphatasia
67
Metabolic bone disease: Hypophosphatasia is a mineralization disorder
True, however it doesn’t have to due to with mineral deficiency. It is the linking of the hydroxyapatite to osteoid that is absent
68
Metabolic bone disease: Histology also changes of HPT
Bone resorption with fibrous tissue replacement
69
Metabolic bone disease: Major bone changes in HPT
Osteopenia Accentuated trabecular pattern Loss of cortical definition BROWN TUMORS Subperiosteal bone resorption
70
Metabolic bone disease: hallmark HPT finding
Superiosteal bone - pathognomonic in the hands
71
Metabolic bone disease: HPT CLinical findings
3:1 Female :male 30-50 yoa Found accidentally by dentist Hypercalcemia, weakness, lethargy, poly dips is, polyuria, renal calculi, bone tenderness
72
AKA for renal osteodystrophy
Uremic osteodystrophy
73
HPT bone changes: In many location but in the middle phalanx of the hands on the radial aspect is pathognomonic 2-4 digits
Subperiosteal bone resorption
74
HPT bone changes: Within harversion canals Linear striations in long bones
Intracortical bone resorption
75
HPT bone changes: Typically hands and with other findings
Endosteal bone resorption
76
HPT bone changes: Common, SI, SC, AC, SP (symphysis pubis), and DV junction, can mimic inflammatory joint disease in SI joint sacroiliitis; DRA (dialysis related arthropathy), DRSA (dialysis related spondylo-arthropathy)
Subchondral bone resorption
77
HPT changes: Diffuse in skeleton, very prominent in cranium, causes very granular appearance to diploic space “salt and pepper” or “pepper pot skull”
Trabecular bone resorption
78
HPT changes: At entheses; trochanters, ischial and humeral tuberosities, elbow, calcaneus, inferior distal end of clavicle
Subligamentous bone resorption
79
HPT changes: localized cyst-like bone resorption containing (overcummulation) fibrous tissue & blood, giant cells and hemorrhages
Brown tumor
80
HPT changes: distal tuft resorption (of fingers), seen with many other conditions - Look at hands!!!
Acro-osteolysis
81
Brown tumor and chondrocalcinosis are common in (primary/secondary) HPT
Primary
82
Osteoscelrosis and periostitis more in (primary/secondary) HPT
Secondary
83
Serum (-) Rheumatoid types
``` Rheumatoid arthritis System lupus erythematous Progressive systemic sclerosis Dermatomyositis/polymyositis Transient: viral infection ```
84
Serum (+) rheumatoid variants
Ankylosing spondylitis Reiter‘ s syndrome aka Reactive arthritis syndrome Psoriatic arthritis Inflammatory bowel disease