Miscellaneous Bone Lesions Flashcards

1
Q

most common cause of dwarfism, which is a congenital hereditary disease of failure of endochondral bone formation

A

achondroplasia

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2
Q

more profoundly affected in achondroplasia (2)

A

femurs and humeri

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3
Q

characteristic finding in this condition is narrowing of interpedicular distances in a caudal direction

A

achondroplasia

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4
Q

lack of blood supply with subsequent bone death and ensuing bony collapse in an articular surface

A

avascular necrosis

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5
Q

manifested by clubbing of fingers and periostitis, usually in the upper and lower extremity, which might or might not be associated with bone pain

A

hypertrophic osteoarthropathy

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6
Q

hypertrophic osteoarthropathy are most commonly seen in patients with

A

lung cancer or other lung disease

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7
Q

rare idiopathic disorder characterized by thickened cortical new bone that accumlates near the ends of long bones, usually only on one side of the bone and has an appearance likened to “dripping candle wax”

A

melorheostosis

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8
Q

group of inherited lysosomal storage diseases characterized by the abnormal accumulation of various mucopolysaccharides such as keratan sulfate and heparan sulfate

A

mucopolysaccharidoses

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9
Q

mucopolysaccharidoses include (2)

A

morquio (keratan sulfate) and Hurler and Hunter (heparan sulfate)

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10
Q

those with mucopolysaccharidoses have what appearance

A

short stature, from shortened spines

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11
Q

mucopolysaccharidoses that has platyspondyly in the spine with central anterior projection of beak off the vertebral body

A

Morquio

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12
Q

mucopolysaccharidoses that has platyspondyly with a beak that is anteroinferiorly positioned

A

Hurler and Hunter

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13
Q

pelvic appearance of wide, flared iliac wings and broad femoral necks are seen in (2)

A

mucopolysaccharidoses and achondroplasia

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14
Q

it has a characteristic finding of pointed proximal fifth metacarpal base that has a notched appearance to the ulnar aspect

A

mucopolysaccharidoses

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15
Q

multiple osteochondromas or exostoses

A

diaphyseal aclasis

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16
Q

cartilage-capped bone outgrowth that may be pedunculated or sessile in appearance

A

osteochondroma

17
Q

widened diameter of bone

A

undertubulation

18
Q

in multiple hereditary exostoses, malignant degeneration are commonly seen in what lesions

A

axial situated lesions

19
Q

painful lesions that occurs almost exlusively in patients less than 30 and is treated successfully with surgical excision or thermal ablation. it is a cortically bases sclerotic lesions in a long bone that has a small lucency within it that is called a nidus

A

osteoid osteoma

20
Q

what causes pain in osteoid osteoma

A

nidus and the surrounding sclerosis

21
Q

5 conditions that present with periostitis without underlyng bony lesion

A
  • trauma,
  • hypertrophic pulmonary osteoarthropathy,
  • venous stasis,
  • thryoid acropachy,
  • pachydermoperiostosis

TV-HPT

22
Q

how to differentiate osteoid osteoma from osteomyelitis

A

the nidus in osteoid osteoma is vascular, it avidly accumulates bone scanning agents and demonstrates double density sign. osteomyelitis has an avascular central photopenic area

23
Q

also known as osteopathia striata, manifested by multiple 2 - 3 mm thick linear bands of sclerotic bone aligned parallel to the long axis of a bone. usually affects long bones and asymptomatic

A

Voorhoeve disease

vOOrhOeve disease = OsteOpathia striata

24
Q

is a hereditary, asymptomatoc disorder that is usually an incidental finding of multiple small (3 to 10 mm) sclerotic bony densities affecting primarily the ends of long bones and pelvis. it has no clinical significance but can be confused for diffuse osteoblastic metastases

A

osteopoikilosis

osteopoikilosis = poiko = polkadot = multiple small sclerotic bony densities

25
Q

rare familial disease that is manifested by thickening of the skin of the extremities and face, clubbing of the fingers and widespread periostitis. occassionally painful

A

pachydermoperiostosis

pachy = thickening; dermo = skin; perio =periostitis

26
Q

in sarcoidosis of MSK, what is particularly involved

A

hands (most common), with spine and long bones

27
Q

causes lacelike pattern of bony destruction in the hands

A

sarcoidosis

28
Q
  1. an idiopathic process that begins with a painful hip with no underlying disorder or other findings other than osteoporosis which is limited to the painful hip. Painful bone marrow edema has been reported in the hip, knee, distal clavicle, and ankle.
  2. A similar process occurs in the knee. It is seen most commonly in the medial condyle but can occur laterally or in the proximal tibia adjacent to the joint.
  3. It can occur in several different locations over time or simultaneously and then is called
A

transient osteoporosis of the hip / idiopathic transient osteoporosis of the hip (ITOH)

painful bone marrow syndrome

regional migratory osteoporosis.