Ortho, Rheum, Etc Flashcards

1
Q

Proximal medial tibia fracture or odd appearance, bowing

A

Blount disease

- Usually diagnosed by 4 yo, but can occur in infants or adolescents

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2
Q

Subtle medial slippage of epiphysis of femoral head

A

Slipped capital femoral epiphysis (SCFE)

  • Obese adolescent with knee pain (referred)
  • Dx: Get AP frog leg view
  • Tx: Immobilize and avoid weight bearing. Surgery
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3
Q

Irregular shaped and jagged femoral head

A

Legg-Calve-Perthes Disease

  • idiopathic avascular necrosis or osteochondrosis of the femoral head
  • Usually diagnosed by 8 yo, usually painless limp but can have hip pain
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4
Q

Breakdown of the tibia at the point of insertion of the patellar tendon, prominence at the tibial tuberosity

A
Osgood Schlatter Disease
Aka Tibial tuberosity apophysitis
- Active adolescent or child in growth spurt, with pain below the knee
- Traction at the tibial tubercle
- Dx: Get lateral X-ray
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5
Q

Salter Harris fracture

A

SMACK mnemonic
• S: slipped (type I)
• M: metaphyseal (type II)
• A: articular-epiphyseal (type III)
• C: complete-metaphysis and epiphysis (type IV)
• K: krushed! (type V) X-ray might look normal or have posterior fat pad

Type III and IV usually require open reduction.
Type V has worse prognosis

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6
Q

Dislocated shoulder

A
usually ANTERIOR (posterior is rare) and >10yo
Dx:  Axillary view X-ray
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7
Q

Valgus deformity

A

Outward angulation of the distal part of the bone/joint

Ex. “Knock knees”

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8
Q

Varus deformity

A

Inward angulation of the distal part of the bone/joint
Ex. “Bow legs”
Ex. Talipes equinovarus deformity, aka “club foot”

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9
Q

Protuberance on one side of the bone with no fracture or deformity on the other side of the bone, usually at the diaphysis

A

Torus fracture (aka Buckle fracture)

  • Compression of bone from longitudinal force
  • Does NOT go through growth plate
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10
Q

Genu varum

A

Bowed legs

  • Normal in <1yo
  • Pathologic if: gets worse after 1yo, persists after 2yo, or presents after 2yo
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11
Q

Intoeing

A
  • Tibial torsion: Toddlers (Two years old)
  • Femoral anteversion: pathologic if persists after 8yo
  • Metatarsus adductus
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12
Q

Scoliosis - treatment

A

<25 degrees: Observe
25-40 degrees: Brace while child is growing
>40 degrees: Surgery

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13
Q

Strain vs sprain

A

Strain = Muscle injury/tear (“sTruscle injury”)
Sprain = ligament injury/tear. (“Sprigment injury”)
Tx: Rest-Ice-Compression-Elevate

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14
Q

ACL tear

A

(+) anterior drawer sign
Dx: MRI
Tx: Surgery

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15
Q

Arthrocentesis

A
Joint aspiration
Indicated for any concern for septic arthritis
-Normal: Yellow fluid,  WBC<200 
-Traumatic tap:  WBC<2000
-Inflammatory or infectious:  WBC >2000
-SLE:  WBC>5000 and normal viscosity
-Rheumatic fever:  WBC>5000 and LOW viscosity
-JRA: WBC ~15,000 and LOW viscosity
-Septic arthritis:  WBC>50,000
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16
Q

Juvenile Rheumatoid Arthritis

A

aka Juvenile Idiopathic Arthritis
<16yo, symptoms >6 weeks, LARGE joints
-Rheumatoid nodules are rare
-Rh factor is not diagnostic but indicates poorer prognosis
-Tx: NSAIDs -> Steroids
-Oligoarticular/pauciarticular=4 or fewer joints, assoc with chronic uveitis
-Polyarticular=5 or more joints, few systemic sx
-Systemic (aka Still’s disease)=Evanescent rash, serum WBC>30, fever, LAD, HSM, Koebner phenomenon, pleurisy, pericarditis. Serum markers NEGATIVE

17
Q

Systemic lupus erythematosus

A
  • Sx: at least 4 of: arthralgias/arthritis, fatigue, malar rash, photosensitive, discoid lesions, oral/nasal ulcers, fever, wt loss, hematologic abnormalities, nephritis (low C3 and C4)
  • Dx: ANA (sensitive), anti-DNA (sensitive), anti-Smith (specific)
  • Tx: NSAIDs, steroids, hydroxychloroquine, methotrexate
  • Neonatal SLE: maternal antibodies. Causes third degree AV heart block. Check anti-Ro/La (aka SS-A, SS-B)
  • Drug-induced SLE: AEDs, sulfa meds, lithium, hydralazine, quinidine. Reversible.
18
Q

Juvenile Reiter syndrome

A

Seroneg spondyloarthropathy
“can’t see, can’t pee, can’t climb a tree”
-Uveitis/iritis
-Urethritis
-Arthritis
Often preceded by infection with Salmonella, Shigella, Yersinia, Chlamydia

19
Q

Behcet syndrome

A

Aphthous and genital ulcers
Uveitis
Arthritis
GI symptoms (distinguishing feature)

20
Q

Sjogren syndrome

A

Can have renal tubular acidosis
Next step: Schirmer’s test (paper to eye)
To confirm: Biopsy lip or salivary gland

21
Q

Wegener’s granulomatosis

A

(+) C-ANCA

Sinuses, lungs, and kidneys