Musc Skel Flashcards

1
Q

Paget’s appearance on XR

A

cotton ball appearance

widened bone with coarse trabecular marking

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2
Q

Incr risk of ____ with Paget’s

A

osteosarcoma

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3
Q

Name each condition
A) brittle bone disease, genetic
B) softening of bones, Vit D or Ca deficiency
C) rare inherited, bones become more dense
D) infection of bone or bone marrow

A

A) osteogenesis imperfecta
B) Rickets (in adults, osteomalacia)
C) osteopetrosis
D) osteomyelitis

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4
Q
Paget's T or F
A) aka osteitis deformans
B) decreased osteoclast / blast activity
C) elevated alk phos
D) narrow trabeculae of osteoid
A

A) T
B) F accelerated activity, incr bone turnover
C) T
D) F mosaic pattern of lamellar bone

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5
Q

In Paget’s a fracture is characterized by

A

breaking straight across

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6
Q

MC organism assoc with osteomyelitis

A

Staph aureus

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7
Q

With osteomyelitis, children are mostly affected in the ____ bones while adults are mostly affected in the ____ bones

A
children = long bones
adults = vertebrae and pelvis
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8
Q
Bone cysts: solitary or aneurysmal?
A) honey-combed appearance
B) occur in metaphysis of long bns, vertebrae
C) occur in distal ends long bones
D) symmetrical
A

A) aneurysmal
B) aneurysmal.
C) solitary
D) solitary

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9
Q

Condition assoc w deficiency of Type 1 collagen

A

osteogenesis imperfecta

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10
Q

avascular osteonecrosis of the epiphysis of the femoral head

A

legg-calve-perthes

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11
Q
Osteoporosis: primary or secondary?
A) advanced age
B) immobilization
C) hyperparathyroidism
D) menopause
A

A) primary
B) secondary
C) secondary
D) primary

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12
Q
Bone cysts: solitary or aneurysmal?
A) occurs in young men
B) occurs in females in 20s, 30s
C) recurrence common
D) cavity filled w clear/bloody fluid
A

A) solitary
B) aneurysmal
C) aneurysmal
D) solitary

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13
Q

MC type of joint disease

A

osteoarthritis

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14
Q

Histo of osteroarthritis

A

fibrous lined cysts in subchondral bone, osteophytes

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15
Q

The breakdown of articular cartilage is triggered by the release of ____ by chondrocytes

A

cytokines such as IL-1 IL-6 and TNF-alpha

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16
Q

Nodules on DIPS?

Nodules on PIPS?

A

Heberden’s nodes

Bouchard’s nodes

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17
Q

Changes within the joint in ostearthritis

A

joint space narrowing, bone spurs, subchondral bone cysts

18
Q

Bilateral, symmetrical fusiform swelling and redness of PIPs, MCT, MTP

19
Q
JIA or RA?
A) subcutaneous nodules infrequent
B) more joint pain
C) 80% of cases assoc w RF
D) more frequent high fever, rash, LAD
A

A) JIA
B) RA
C) RA (vs 10-20% in JIA)
D) JIA

20
Q

MC GU infx that precedes reactive arthritis

21
Q

Name for clinical triad of RA, including splenomegaly and manifestations of hypersplenism

A

Felty’s syndrome

22
Q

Genetic mutation for most seronegative spondyloarthropathies?

23
Q
RA, AS, PA, Reactive or Septic?
A) Axial skeleton is affected
B) Affects DIPs
C) proliferative exudative synovitis 
D) dactylitis
A

A) AS
B) PA
C) RA
D) reactive, PA

24
Q

Calcium pyrophosphate dehydrate crystals (bifringent) deposit in knees/ankles

A

Pseudogout

25
Pathognomonic lesion of gout
tophus, MTP 1
26
Viral causes of arthritis
Parvo B19, rubella, Hep C, HIV
27
Crystal that causes gout
uric acid
28
``` Causes septic arthritis (organism) A) elderly, immunocomp B) MC older children/adults C) 2nd MC cause D) Sickle cell pts ```
A) E coli B) Staph aureus C) Strep spp D) Salmonella
29
T or F | Reactive arthritis is caused by pathogens infecting the joints
F, arthritis is caused by antibody response to LPS in cell wall of organism. The organisms themselves do not infect joints.
30
Reactive arthritis triad
non-gonococcal urethritis or cervicitis, conjunctivitis, and arthritis
31
``` RA, AS, PA, Reactive or Septic? A) pitting of nails B) HLA-DR4 C) follows GU and GI infx D) hyperplastic synoviocytes ```
A) PA B) RA C) reactive D) RA
32
MC form of muscular dystrophy
Duchenne's
33
Poly, dermatomyositis, or Inclusion body? A) no skin involvement B) T8 lymphocyte infiltration C) periorbital heliotrope rash and Gottran's sign D) 50% of cases dt paraneoplastic syndrome
A) poly B) poly C) dermato D) dermato
34
X-linked inability to produce dystrophin, resulting in excess Ca++ causing oxidative stress (death of cell)
Duchenne's
35
MG or Lambert-Eaton? A) Ab block Ach receptors post synapse B) Assoc w small cell lung CA C) Abs target presynaptic Ca++ channels, inhibiting Ach release
A) MG B) LE C) LE
36
People with MG also tend to have abnormalities of the _____. What form of abnormality in males? females?
thymus thymoma in males thymic hyperplasia in females
37
MG or Lambert-Eaton? A) lymphocytes; pale/atrophic muscle fibers B) better w initial exertion, then worse C) worse activity / better rest
A) MG B) LE C) MG
38
Poly, dermatomyositis or Inclusion body? A) adults; rare/nonexistent in persons younger than 20 B) slowly progressive weakness and wasting of distal and proximal muscles C) mixed B and T cell inflamm infiltrate D) dysphagia is a poor prognostic sign
A) poly B) inclusion C) dermato D) poly
39
focal areas of white blood cells and other inflammatory cells, the appearance of vacuoles in the muscle, deposits of amyloid-related proteins within the muscle cells
inclusion body myositis
40
Muscles fibers appear | pale & enlarged, invasion by macrophages
polymyositis
41
Inflammatory cells invading muscle Necrotic muscle fibers under inflammatory cells Regenerating muscle fibers.
dermatomyositis
42
Arthritis assoc with IBD, IgG associated
enteropathic arthritis