metabolic bone disease Flashcards

1
Q

What is osteoporosis?

What is osteomalacia?

A

Decreased bone QUANTITY

Decreased bone QUALITY with normal quantity

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2
Q

How many cases are secondary osteoporosis vs primary?

A

5% are secondary (due to an underlying pathology)

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3
Q

How is osteopenia diagnosed?

A

cortical thinning

usually in the 2nd or 3rd metacarpal, the cortical width should be ~1/3 the bone shaft width

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4
Q

Which is more effective in alleviated post menopausal osteopenia?

A

Estrogen

No proof that calcium helps

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5
Q

What is the difference between primary osteoporosis and disuse osteoporosis?

How can disuse be differentiated from a permeative bone lesion?

A

Disuse occurs more rapidly and has a patchy appearance

The cortex will be intact in disuse

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6
Q

What is meant by the term pseudopermeative? What causes it?

A

Permeative appearance of the cortex due to cortical holes

Malignancy
Hmangioma
Radiation

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7
Q

What is the differential for a permeative marrow if 30?

Pseudopermeative?

A

Ewings, Infection, EG

Lymphoma, Infection, Myeloma, Mets

Aggressive osteoporosis, hemangioma, radiation changes

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8
Q

What is the most common cause of osteomalacia?

A

Renal osteodystrophy

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9
Q

What finding is pathognomonic for osteomalacia?

A

Looser fracture

fracture through large osteoid seams

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10
Q

What are the radiographic signs of rickets?

A

Pediatric osteomalacia

Flared and irregular epiphyses with long bone bending

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11
Q

What is the most common cause of hyperparathyroidism?

A

Renal disease causing secondary hyperparathyoidism

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12
Q

What are the radiographic findings in hyperparathyroidism?

A

Subperiosteal bone resorption - commonly seen in the 2nd and 3rd radial middle phalanges

Clavicular osteoclysis

Osteosclerosis - rugger jersey spine

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13
Q

What are the findings of hypoparathyroidism?

A

Calvarial thickening and basal ganglia calcification

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14
Q

What is pseudohypoparathyroidism? What are the radiographic findings?

What is pseudopseudohypoparathyroidism?

A

End organ failure with normal pituitary and PTH. Brachydactyly within the tubular bones of the hand

Clinical pseudohypoparathyroidism with no end organ or pituitary abnormality

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15
Q

What happens with adenohypophysis tumor/hyperplasia if the growth plates are closed/open?

A

Closed - acromegaly

Open - gigantism

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16
Q

What are the findings in acromegaly?

A

Calvarial thickening, enlarged sinuses, enlarged sella turcica

Prognathia

Hypertrophied “spade” appearance distal phalangeal tuft

Mild joint space widening due to cartilage overgrowth

Soft tissue thickening, such as the fat pad medial to the calcaneus

17
Q

What is thyroid acropachy?

A

Occurs after thyroidectomy

Periostitis of the metacarpals and phalanges, prominently the ulnar aspect of the fifth metacarpal

18
Q

Delated epiphyseal closure (30-40yo) and stippled epiphyseal appearance is seen with what disease?

A

Hypothyroidism in children

19
Q

What is the differential for osteosclerosis?

A
Renal osteodystrophy
Sickle cell
Myelofibrosis
Osteopetrosis
Pyknodysostosis
Mets
Mastocytosis
Pagets
Athletes
Fluorosis

Regular Sex Makes Occasional Perversions Much More Pleasureable And Fantastic

20
Q

What are the signs of sickle cell disease?

A

Fish vertebrae - step off deformities of the vertebral body endplates

Hip AVN

Bone infarcts

21
Q

When should myelofibrosis be considered with osteosclerosis?

What else to look for?

A

> 50yo

Look for splenomegaly and extramedullary hematopoiesis

22
Q

What is osteopetrosis? What are the types

What are the radiographic findings?

A

Congenital - can be fatal, anemia, jaundice, hepatosplenomegaly, infections

Tarda - milder clinical presentation

Bone in bone appearance of the spine - small replica of vertebral body inside the normal one

Sandwich spine - densely sclerotic endplates similar to rugger jersey spine, though this will be denser than PHPT

23
Q

What is pyknodysostosis?

What are the findings? What is pathognomonic of this condition?

A

Dense sclerosis of the bones

Short stature, hypoplastic mandibles

Acroosteolysis with sclerosis “Chalk phalanges put into sharpener”

24
Q

What are the findings in mastocytosis?

A

Uniform sclerosis

Thickend GI folds with nodules
Urticaria pigmentosa

25
Q

What are the findings in Pagets disease?

Where does it classically present? What is a classic sign?

A

Bony enlargement with three distinct phases
1 - lytic
2 - sclerotic
3- mixed

Pelvis

Iliopectineal line thickening

Always starts at the end of the long bone (except tibia)

26
Q

What are the three phases of Pagets?

A

Lytic - flame shaped or blade of grass
Sclerotic
Mixed

27
Q

Where does paget affect long bones classically?

A

Ends extending centrally

If there is a central lesion, pagets can be ruled out

28
Q

What is fluorosis?

What is the classic finding?

A

Chronic intake of fluoride

Ligamentous calcification

Sacrotuberous ligament calcification

29
Q

What is the teardrop sign with regards to joint effusion?

A

The distance from the most medial part of the femoral head to the most medial extent of the acetabulum (teardrop).