Lec 22 Pediatric Rheumatology Flashcards

1
Q

What are the 3 subtypes of juvenile chronic arthritis?

A
  • systemic
  • polyarticular
  • pauciarticular
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2
Q

What type of JRA has best vs worst prognosis for joints?

A
best = systemic or pauciarticular
worse = polyarticular RF+ girls
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3
Q

What type of JRA has worst prognosis for life?

A

worst = systemic

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4
Q

What are symptoms of systemic JRA?

A

arthritis, fever, rash, serositis, organomegaly, leukocytosis

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5
Q

What are symptoms of polyartricular JRA?

A

fever, anemia, malaise

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6
Q

What are symptoms of pauciarticular JRA?

A

have iriocyclitis –> uveitis/iritis

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7
Q

What are signs of adult still’s disease?

A
arhtralgias/arthritis
maculopapular rash --> salmon colored rash on trunk only present in height of fever
spiking fevers
seronegative
lymphadenopathy
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8
Q

What is treatment for JIA?

A

methotrexate

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9
Q

What is macrophage activation syndrome?

A

life threatening complication of still/systemic JIA

have immune activation of T cells and macrophages –> pancytopenia; hyperferritinemia

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10
Q

What happens in stage 1 lyme disease?

A

erythema migrans

flu like syndrome

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11
Q

What happens in stage 2 lyme disease?

A

early disseminated –> recurrent erythema migrans; migratory arthritis; meningoencephalitis; bell’s palsy; carditis

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12
Q

What is treatment for lyme disease?

A

doxycycline early in disease

amoxicillin in kids

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13
Q

What are most common organisms in septic arthritis in adults?

A

staph aureus; strep; neisseria gonorrhoae/meningitidis

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14
Q

What are most common organisms in septic arthritis in kids?

A

staph aures, strep pyogenes, H influenza

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15
Q

Who gets gram negative septic arthritis?

A

IV drug users

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16
Q

What is kawasaki clinical picture?

A
  • spiking fever for at least 5 days
  • bilateral conjunctival congestion
  • oropharynx invovlement
    strawberry tongue
17
Q

How do you treat kawasaki?

A

IV Ig

18
Q

What do you see in neonatal lupus?

A

rash on face and upper trunk –> from Rh+ kid with Rh- baby –> get skin disease that goes away in 3-4 months

19
Q

What are clinical feat of myositis?

A

proximal muscle weakness
dysphagia
high muscle enzymes

20
Q

What antibodies seen in myositis?

A
  • anti-synthetase syndrome –> Ab against aminoacyl-tRNA synthetases
  • anti Jo-1