Part 17 Flashcards

1
Q

AVN of lunate

A

Keinbock’s disease

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2
Q

who gets Keinbock’s?

A

people who do manual labor

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3
Q

what is keinbock’s associated with?

A

negative ulnar variance

progressive pain + soft tissue swelling of wrist

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4
Q

radiographic features of Keinbock’s

A
initially increase in density of lunate
later fragmentation and collapse
mixture of sclerosis and radiolucent
flattening, collapse and fragmentation
altered joint congruity and biomechanics precipitates DJD
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5
Q

what is the possible treatment for Keinbock’s?

A

silastic implants

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6
Q

tarsal navicular AVN

A

Kohler’s

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7
Q

signs and symptoms of Kohler’s

A

localized pain, swelling

navicular patchy, homogenous sclerosis, collapse fragmentation

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8
Q

scheuermann’s disease etiology

A

in question, probably doesn’t represent a necrosis, likely TRAUMA

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9
Q

what is scheuermann’s disease?

A

abnormality of the discovertebral junction
usually in teens
chronic back pain, deformity and early DDD

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10
Q

radiology of scheuermann’s

A
thoracic and lumbar spine
3 continguous vertebra
5 degree anterior body wedging
irregular end plates
decreased disc space
increased kyphosis
schmorl's nodes
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11
Q

etiology of juvenile discogenic disease

A

failure of embryonic vascular channels, centrum defects, notochord clefts to disappear, leaving endplate defects

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12
Q

juvenile discogenic disease produces?

A

early degeneration, segmental dysfunction, associated pathology of the facet joint

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13
Q

sever’s disease

A

NOT a necrosis
sclerosis and fragmentation of the calcaneal apophysis represents normal anatomy
correlate clinically

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14
Q

calcified medullary infarct

A

serpiginous regions of calcification within the bone medulla

usually associated with arteriosclerosis

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15
Q

DDx of serpiginous regions of calcification within bone medulla

A
  1. enchondroma
  2. chondrosarcoma
  3. calcified medullary infarct
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16
Q

MC hemolytic anemia

A

sickle cell

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17
Q

what demographic MC gets sickle cell anemia?

A

african americans

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18
Q

signs/symptoms of sickle cell anemia

A

pain and swelling in hands and feet
infarct of bowel following obstruction of mesenteric arteries (abdominal crisis)
osseous changes related to infarction, AVN, marrow hyperplasia and retarded growth

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19
Q

those with sickle cell anemia are predisposed to what?

A

salmonella osteomyelitis

gallstone problems

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20
Q

radiographic findings of sickle cell anemia

A
marrow hyperplasia
coarse trabeculation
osteopenia
long bone undertubulation
hair on end skull
osteonecrosis/infarct
H shaped vertebra
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21
Q

thalassemia AKAs?

A

cooley’s anemia

medeterranean thalassemia

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22
Q

presentation of thalassemia

A
fatigue due to chronic anemia
splenomegaly
cardiomegaly
gallstones
marrow hyperplasia
extramedullary hematopoiesis
maxillary overgrowth (rodent faces)
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23
Q

radiology of thalassemia

A
coarsened trabeculation (honecomb/lace like)
osteopenia
erlenmeyer flask deformity
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24
Q

background of hemophilia

A

X chromosome linked bleeding disorder

female the carrier usually manifest in males

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25
imaging for hemophilia
``` intra-articular soft tissue swelling radiodense effusion osteopenia square femoral condyles degeneration epiphyseal overgrowth erosions ```
26
clinical features of hemophilia
joint pain | hemophilic arthropathy
27
background for leukemia
malignant proliferation of WBCs
28
imaging for leukemia
``` radiolucent submetaphyseal bands osteopenia osteolytic destruction of long bone metaphysis and diaphysis periosteal reactions growth arrest lines ```
29
clinical features for leukemia
``` fever malaise joint pain easily bruised spontaneous bleeds ```
30
cellulitits
infection of skin, subcutaneous fat or connective tissue
31
osteomyelitis
infection of bone (marrow spaces)
32
septic arthritis
infection of joint
33
those who are at risk for infection
``` immunosuppressed diabetics post-surgical vascular insufficiency sickle-cell anemia IV drug users ```
34
where are drug addicts prone to getting infection?
spine sacroiliac symphysis pubis sternoclavicular
35
what is the most common organism for an infection?
staph aureus
36
modes of infection
``` trauma/post surgerical UTI pneumonia skin infections open wounds or cellulitis heel sticks in infants ```
37
routes of dissemination
hematogenous (MC) direction extension direct implantation postoperative
38
infants and young adults may present with what when they have an infection?
``` fever chills pain swelling loss of limb function elevated ESR elevated WBC ```
39
adult patterns of infection
``` fever malaise edema erythema pain ```
40
50% of those with infection previously had?
skin, respiratory or genitourinary tract infections
41
suppurative osteomyelitis
2-12 years | males
42
infantile pattern of vasuclar anatomy
metaphyseal and diaphyseal vessels may penetrate the physis (septic arthritis and osteomyelitis)
43
childhood pattern of vascular anatomy
1 year to physis closure, metaphyseal blood flow is slow and turbulent, metaphyseal vesself don't penetrate physis, separate epiphysis blood supply
44
adult pattern of vascular anatomy
metaphyseal vessels penentrate the vanishing physis, reestablishing communication with the subarticular bone end (osteomyelitis and septic arthritis)
45
most common locations of hematogenous infection
``` knee hip ankle (distal tibia) shoulder spine ```
46
two major categories of infections
suppurative (pus)- staph | non-suppurative (TB)
47
suppurative osteomyelitis
``` bone marrow infection by (pyogenic) non tubercular organism (anything but TB) staph aureus strep pneumoniae e coli pseudomonas ```
48
clinical features of acutre infections
``` edema lyphadenopathy warm skin cellulitis joint pain ```
49
4 radiographic stages of osteomyelitis
``` latent stage (1-10 days) early stage (10-21 days) middle stage (weeks) late stage (months) ```
50
early stage of osteomyelitis
spinal lesion may approach 3 weeks soft tissue edema osteopenia
51
middle stage of osteomyelitis
``` permeative or lytic moth eaten descruction perosteal responase (solid laminated, codman's triangle) ```
52
buttressing/solid periosteal reaction
when additional layers of new bone are added to the exterior creating an expended osseous contour usually associated with slow growing lesions
53
laminated/layered/onions skin
multiple layers of new layers of bone alternating layers of lucency and opacity with alternating growth can be thick or thin can be seen in slow or aggressive lesions classically associated with ewing's
54
spiculated
linear radiating spicules of new bone
55
hair on end
when spiculated bone is perpendicular to the bone
56
sunburst
when the spiculated bone is radiating from a central focus
57
codman's triangle
triangular elevation of periosteum seen at the periopheal lesion cortex junction is one of themost aggressive forms of periosteal reaction may be seen also with benign tumors, infections or other disorders
58
late stage osteomyelitis
``` cortical destruction draining sinus involucrum cloaca sequestrum sclerosis debris loss of joint space ankylosis chonic incomplete resolution immune deficient ```
59
sequestrum
chalky, white area representing isolated dead bone | cortical and medullar infarcts
60
involucrum
"bony collar" (chronic periosteal response | pus lifts the periosteum and causes new bone formation, trying to wall off the infection
61
cloaca
rare compilation is to devlop a squamous cell carcinoma within the channel of the cloaca
62
malignant transformation of cloaca
Majolin's ulcer