Rheum Flashcards

1
Q

ankylosing spondylitis mainly affects

A

SI joints

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2
Q

ankylosing spondylitis more common in

A

males

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3
Q

ankylosing spondylitis associated with

A

IBD

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4
Q

bamboo spine on xray

A

ankylosing spondylitis

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5
Q

night pain and morning back stiffness relieved by exercise

A

ankylosing spondylitis

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6
Q

shiny or scaly skin over the interphalangeal joint

A

gottron’s sign (dermatomyositis)

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7
Q

heliotrope rash, shiny/scaly extensor surfaces and interphalanges, difficulty getting dresses, voice change/difficulty swallowing

A

dermatomyositis

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8
Q

most common systemic vasculitis in children

A

HSP

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9
Q

palpable purpura, heme positive stool, colicky abdominal pain, hematuria

A

HSP

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10
Q

most common rheumatologic disease of childhood

A

JIA

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11
Q

JIA must present before what age

A

16 (at least 6 weeks in 1 joint)

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12
Q

morning stiffness with gradual loss of motion and rash

A

JIA

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13
Q

ANA in JIA

A

usually positive

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14
Q

JIA is more common in

A

girls

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15
Q

polyarthritis JIA

A

5 or more joints in the first 6 months, most females

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16
Q

oligoarthritis/pauciarthritis JIA

A

4 or fewer joints during the first 6 months, ANA positive, usually young females, associated with chronic uveitis, boys w/ HLA b27 have a better prognosis

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17
Q

systemic onset JIA

A

aka stills disease, affects males and females equally, extraarticular involvement is common

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18
Q

enthesitis related arthritis

A

SI joint pain, more common in boys, HLA-B27

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19
Q

first line JIA treatment

A

NSAID (indomethacin, ibuprofen, naproxen)

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20
Q

2nd line JIA treatment

A

steroids and immunosuppressants if NSAIDs don’t work

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21
Q

MTX MOA

A

folate antagonist - side effects = GI distress and pulmonary toxicity

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22
Q

gold standard therapy for JIA

A

methotrexate

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23
Q

mucocutaneous lymph node syndrome aka

A

kawasaki’s

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24
Q

Kawasaki is more common in

A

asian, males, around 2 years old, mostly winter and spring

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25
Kawasaki's criteria
high fever for at least 5 days plus at least 4 - cervical LAD - cracked lips - non-exudative conjunctivitis - polymorphous exanthem on trunk - erythema/ desquamation of hands/feet
26
things common in Kawasaki that are not part of the criteria
sterile pyuria, migratory poly arthritis, gallbladder hydrops, thrombocytosis
27
thrombocytosis by what day with kawasaki
day 5
28
leukocytosis by what day with kawasaki
day 12
29
Kawasaki treatment
IVIG 2g/kg, initial high dose aspirin of 80mg/kg/day x24-48 hours then maintenance aspirin of 5 mg/kg/day x2 months
30
what vaccines can't be given after IVIG
varicella and MMR cannot be given for 11 months after IVIG
31
Lyme disease is carried by
ixodes deer tick
32
ticks need to feed how long to transmit lyme disease
36 hours
33
erythema chronic migrans
lyme disease
34
second stage of lyme disease
carditis, arthritis, neurologic (Bell's palsy)
35
treatment for Lyme disease if less than 8
amoxicillin
36
treatment for Lyme disease if less than 8 and penicillin allergic
cefuroxime
37
chills, fever and hypotension after treatment for lyme disease
jarisch-herxheimer reaction due to lysis of organism and release of endotoxin
38
urethritis, iritis and arthritis
reactive arthritis
39
most common cause of reactive arthritis in the US
chlamydia trachomatis
40
reactive arthritis in kids is usually after
enteric infection
41
weight loss and fatigue with hilar adenopathy
sarcoidosis
42
granulomas in sarcoidosis
noncaseating but can secrete vitamin D causing hypercalcemia and hypercalciuria
43
arthritis, rash and uveitis
sarcoidosis
44
scleroderma is more common in
females
45
sclerodactyly, pulmonary fibrosis and reflux
systemic scleroderma
46
linear hyperpigmented patch and shiny hypo pigmented skin with a brown border
localized linear scleroderma
47
SLE diagnosis requires
4 or more - malar rash - discoid lesions - photosensitivity - oral ulcerations - arthritis - hematologic abnormalities - renal abnormalities - anti-ds-DNA, and-DNA and anti-Smith Ab's - psychosis - positive ANA
48
antibody specific to SLE
anti-ds-DNA and anti-smith DNA
49
how to track severity of disease in SLE
anti-ds-DNA levels (fluctuate accordingly) or C3 and C4 levels (inversely proportional)
50
rash on trunk and bradycardia with 3rd degree heart block in newborn
neonatal lupus
51
most common cause of death in an infant born to a mom with SLE
heart block
52
antibody associated with neonatal lupus
anti-SSA antibody (anti-Ro) and anti-SSB (anti-la)
53
mild lupus treatment
NSAIDs and hydroxychloroquine
54
hydoxychloroquine side effects
blurring of vision to permanent retinal damage and ototoxicity
55
treatment for lupus with severe organ involvement
cyclophosphamide
56
complications associated with high dose steroids
cataracts, glaucoma, osteoporosis, HTN, glucose intolerance, cushingoid features
57
ANA pattern in mixed connective tissue disease
speckled ANA
58
antibody in mixed connective tissue disease
anti-U1 ribonucleoprotein antibody (anti-U1 RNP)
59
diagnosis in child with systemic JIA now with elevated LFTs, positive d-dimer, prolonged PTT and cytopenia
macrophages activation syndrome
60
diagnosis with arthritis, dactylics and pitting of nails
juvenile psoriatic arthritis
61
fever, weight loss, migratory arthralgia, nodules in lungs, elevated creatinine, positive c-ANCE
granulomatosis with polyangitis (Wegener's)
62
pathergy test
prick skin with needle, pustule or papule surrounded by redness forms within 48 hours with Behcet disease
63
painful recurrent oral and genital ulcers and uveitis
Behcet disease
64
antibody that is likely the cause of miscarriages in lupus
antiphospholipid antibodies
65
recurrent parotitis, dry eyes and mouth, anti-Ro positive
sjogren syndrome
66
PFAPA
periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis
67
Turkish girl with fevers for 3 days every 3 months with elevated ESR, CRP and WBC during fevers nut normal in between
familial mediterranean fever