Lecture 6: Rheum & MSK Flashcards

(45 cards)

1
Q

3 Requirements for Dx of Juvenile Arthritis (JIA)?

A
  1. Evid of joint inflammation
  2. CHRONIC arthritis (> 6 wks)
  3. Sxs must have been present at < 16 yrs old
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2
Q

4 signs on PE indicating chronicity of Juvenile Arthritis

A
  1. Synovial thickening
  2. Contracture
  3. Bony proliferation
  4. Limb length discrepancy
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3
Q

Definition of Systemic Juvenile Arthritis/Still’s Dz
(subset of JIA)

What is the typical fever pattern in this dz?

A

Systemic inflammation BEFORE onset of arthritis

daily fever spike of > 39 C –> quickly goes below baseline
- feel fine b/t spikes

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4
Q

4 characteristics of the rash a/w Systemic Juvenile Arthritis/Still’s Dz?

A
  1. at peak of fever
  2. Erythematous maculopapular rash on trunk/extremities
  3. Migrates + fades quickly
  4. Dermatographia
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5
Q
  1. Main thing seen on labs a/w Juvenile Arthritis?
  2. What other lab results a/w JIA?
  3. What is NOT seen in kids in JIA labs?
A
  1. ANA (anti-nuclear Abs)
  2. Evid of systemic inflam (C reactive protein, WBCs, etc)
  3. Rheumatoid factor NOT seen in kids w/JIA
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6
Q

Which type of JIA has the highest prevalence of ANAs
- what is only prob w/ANAs for Dx?

When is Rheumatoid factor positive?

A

Oligoarticular JIA = most ANAs

Rheumatoid factor is positive in adol + adults w/ RA

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7
Q

What is lst line Tx for JIA?

  • when should you switch pts to something else?
  • what are the other 3 Tx options?
A

1st line = NSAIDs
- switch if not working in 1-2 wks

other Tx options

  1. Hydroxychloroquine
  2. Methotrexate
  3. Biologics (-mabs, etc)
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8
Q

What is the main complication of JIA?

Therefore kids w/what dz are required to be screen for this?

A

Uveitis
- note: MC cause of blindness in kids and often Asx

screening required for ALL kids w/chronic arthritis

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9
Q

3 cutaneous manif a/w Juvenile Dermatomyositis (JDM)?

A
  1. Heliotrope rash –> rash around eyes
  2. Gattron’s papules (fingers)
  3. Periungual erythema
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10
Q

Main sign a/w Juvenile Dermatomyositis?
What it is/what is it d/t?

Other signs

  1. Calcinosis/calcif of muscles
  2. Lipotrophy
A

Gower’s sign = child must must hands to “walk own body up from lying prone position to stand
- d/t lack of strength of in hips/thighs (proximal muscle weakness)

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11
Q

What 3 things provide evid of inflammatory myositis in JDM?

A
  1. Muscle enzymes elevated
  2. Muscle Bx
  3. MRI
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12
Q

What is the initial Tx for JDM?

- other tx options?

A

start w/prednisone

  • other: Methotrexate, Cyclophosamide
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13
Q

2 Cutaneous manifestations of Henoch-Schonlein Purpura (HSP)?

note: dz peaks in winter

A
  1. Palpable purpura = MC

2. Edema (hands, feet, face, scrotum)

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14
Q

MC areas and appearance of Palpable Purpura in HSP?

A

MC in dependent areas –> bac of legs/butt

appearance = petechia/macules/urticaria –> ecchymosis

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15
Q

4 things a/w Arthralgia/arthritis see in Henoch-Schonlein Purpura?

A
  1. in large LE joints
  2. v. painful–> refuse to bear wt
  3. joint swelling but usu no erythema
  4. Transient
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16
Q

3 signs a/w GI involvement in Henoch-Schonlein Purpura?

Note: onset = w/in 1wk -1 mo of rash

A
  1. colicky abd pain
  2. heme (+) stools
  3. intestinal perforation
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17
Q

What is the renal involvement in Henoch-Schonlein Purpura (HSP) d/t? 3 things seen w/it?

Note: onset = w/in 1-3 mo of rash

A

d/t acute glomerular nephritis

  1. hematuria/proteinuria
  2. HTN
  3. +/- renal failure
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18
Q

2 things seen on labs a/w Henoch-Schonlein Purpura
- what cannot be present?

Results on pathology?

A
  1. Elevated inflam markers
  2. Normocytic, normochromic anemia
    - CANT HAVE THROMBOCYTOPENIA

Pathology –> IgA deposition w/Leukocytoclastic vasculitis

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19
Q

Classic palpable, non-thrombocytopenic purpuric rash + 1 of following:

  • arthritis or arthralgia
  • abd pain and/or GI blood loss
  • Bx w/IgA deposition

What name of this/dz a/w?

A

EULAR consensus criteria for HSP

20
Q

What is given for Tx of arthritis in HSP?

Tx for severe GI dz or active renal dz?

A

Tx for arthritis = NSAIDs

Tx for severe GI dz or active renal dz = CCS

21
Q

1 y/o pt in February present w/fever for last 5 days, non-exudative bilateral conjuctivitis, swollen/red/cracked lips and tongue and LAD of single cervical node. What is Dx?\

What is name for lip/tongue sign?
Peak months?

A

Dx = Kawasaki Dz

Strawberry lips + tongue

Peak = February - May

22
Q

Nemonic for Dx criteria for Kawasaki Dz and what each stands for?

What if pts present w/4+ ?

A

“FEBRILE”

  1. Fever
  2. Exanthem
  3. Bulbar conjunctivitis
  4. Rash
  5. Internal organ involvement (not part of it)
  6. LAD
  7. Extremity changes

4+ present –> can Dx on day 4 of fever

23
Q

What is the mainstay of Tx for Kawasaki Dz?
- when given and why?

Other medication given in this dz?

A

IVIG
- given w/ 7-10 days of onset of rash –> prevent cardiac complications (HIGH RISK OF CORONARY ARTERY ANEURYSM)

ASA –> once instance where given in kids
(Reye’s Syn)

24
Q

5 y/o comes in complaining of deep aching pain for 6 months that occurs MC in her legs. Her mother said the pain usu occurs after playing or later in day/night. PE was normal. What is Dx and how to Tx?

A

Dx = growing pains
Note: MC in 3-7 y/o & legs, chronic pain

Tx = stretching and reassurance

25
5 y/o pt comes in non-articular bone pain, back pain, bone tenderness, severe wt loss + fever, night sweats and bruising... What is most likely cause?
Cancer
26
What in newborns put them at risk for developing Developmental Dyplasia of Hip (DDH)? Other RFs: female, breech, FHx What are the 2 main presentations of baby w/DDH?
newborns = ligamentous laxity --> spontaneous hip dislocation 1. Asymmetrial Creases 2. Galeazzi's Sign --> asymmetric knee heights
27
Name of the two screening tests for Developmental Dyplasia of Hip/what they are for?
1. Barlow Test = dislocation | 2. Orotolani Test = reduction
28
Tx of DDH for younger kids < 6 mo vs older kids?
young kids < 6 mo --> Pavlik harness --> put hip back in place (usu in 2 wks) older kids --> surgery
29
Why does Avascular Necrosis of the Femoral Head occur? what is it a common complication of? Note: aka Legg-Calve-Perthes Dz
Femoral Head lacks collateral blood supply complication of SCD
30
3 common S/s of Avascular Necrosis of the Femoral Head? What is late sign of dz seen on XR? Tx for kids > 6 y/o?
1. painless limp 2. +/- intermittent LE pain 3. decr internal rotation + abduction of hip Late sign on XR = flattening of femoral head Tx = braces/surgery
31
What d/o is an orthopedic emergency, mainly occurring in adolescents?
Slipped Capital Femoral Epiphysis
32
12 y/o pt presents w/limp, decr ROM and atalgic gait. You notice she is holding her R leg externally rotated position. When you hip her R hip her leg externally rotates and there is limited internal rotation + loss of flexion/extension. Dx? Tx?
Dx = Slipped Capital Femoral Epiphysis - note: if unstable pts cant ambulate at all Tx: NWB status, ortho referral for surgery
33
2 complcations of Slipped Capital Femoral Epiphysis?
1. Chondrolysis | 2. Avascular necrosis
34
What is Osgood-Schlatter Dz? When does it typically occur and boys vs girls?
Microfracture or partial avulsion involving tibial tubercle (TT) Typically after growth spurt - earlier in girls than guys
35
3 s/s of Osgood-Schlatter Dz? Tx = rest, modify activity, ICE, NSAIDs, stretch/exercises
1. knee pain (during/after activ) 2. tender + local swelling (TT) 3. bony enlargement (TT)
36
How to distinguish in-toeing vs out-toeing? How position the child?
Thigh-Foot-Angle Measurements w/child lying prone | - look at angle of foot compared to thigh
37
Other names for Bowleg and Knock Knees only 2 reasons surgery needed?
Bowleg = Genu Varum Knock Knees = Genu Valgum surgery if severe disformities or gait dysfxn
38
What is torticollis? 2 common findings in infants?
shortening of sternocleidomastoid muscle 1. tilt ear towards affected side 2. look up toward contralateral side
39
How does Polydactyly affect Af Am vs Caucasians?
Af Am --> pinky affected (AD inheritance) | Caucasians --> thumb affects
40
3 types of Polydactyly? What type is the only one that doesnt need surg? what is Tx?
Type 1 = soft tissue only --> dont need surg - Tx = ligation or electrocautery Type 2 = duplicate finger +bone/joints Type 3 = duplicate finger + metacarpal
41
What is scoliosis? How detect? When is least likely idiopathic? 2 non-idiopathic causes? How to measure angle of curve? Who more likely to have bigger curve?
Lateral curvature of spine (truncal asymmetry) - w/"forward bend test" Least likely idiopathic in infants (birth - 3 yrs) Non-idiopathic causes: 1. Cerebral Palsy 2. Muscular Dystrophy Cobb angle on Xray bigger curve more likely in females
42
When is bracing considered for scoliosis? Other option/considered when?
bracing: curve 20-40 degrees Other option = surgery - curve > 40 degrees
43
Mechanism for Nursemaid's Elbow why common in < 5
1. Axial traction on pronated forearm + extended elbow --> annular ligament -->trapped in radiohumeral joint "Swinging kids by arm" at age 5 annular ligament strengthened
44
3 y/o boy presents w/arm pain w/active supination. He is holding his arm close to his w/elbow fully extended and forearm protonated. What should you do to Tx his condition?
Tx = Radial Head Subluxation | for Nursemaid's Elbow
45
Steps of Radial Head Subluxation for Tx of Nursemaid's Elbow
1. thumb on radial head 2. apply longitudinal traction 3. supinate forearm 4. flex elbow