peds rheum Flashcards

(45 cards)

1
Q

JIA

A

prolonged fever, salmon patch rash, arthritis, visceral involvement

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2
Q

scarlet fever

A

strawberry tongue, bilateral cervical LAD, fever, rash

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3
Q

rheumatic fever

A

Rash, subcutaneous nodules, fever, polyarthralgia, chorea

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4
Q

viral syndrome (enterovirus)

A

Fever 3-5 days, non-descript non-painful rash, can walk

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5
Q

kawasaki

A

fever > 5days, nonpurulent conjunctivitis, erythematous rash, swelling and erythema of extremities, unilateral LAD

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6
Q

osteomyelitis/septic joint

A

Low grade fever, painful walking

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7
Q

RMSF

A

Fever

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8
Q

Steven johnson

A

Severe pruritic rash, fever

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9
Q

measles

A

conjunctivitis, fever, rash, non-immunized

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10
Q

kawasaki

A

Mucocutaneous lymph node syndrome

Acute Febrile Vasculitic syndrome of early childhood

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11
Q

kawasaki symps list

A

Supporting Sx: Non-remitting High grade Fever > 5 days PLUS 4/5 of the following:
red macpap rash
unilat cerv adeno>1.5 cm
strawberry tongue, red fissurd lips, injected pharynx
non-pur. conjunc, bilat, painless
redness/swell of hands/feet
desquamations of tips, transfers grooves across nails -beau lines)

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12
Q

kawasaki labs

A

No specific diagnostic test; Elevated ESR/CRP, Anemia, Elevated WBC, Thrombocytosis, Hypoalbuminemia, Elevated AST/ALT
Case: Echocardiogram with coronary artery aneurysms

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13
Q

kawasaki complications

A
coronary artery aneurysm
CNS manifest (mening.)
liver dysfunc
arthritis
hydrops of gall bladder
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14
Q

kawasaki pathoma

A
Kawasaki Motorcycle
Hold on with Palms and Soles:
Edema
Erythema
Desquamation
Heart Racing: CAA
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15
Q

kawasaki tx

A

Usually self-limiting ~12 days
BUT leads to significant morbidity and mortality
IV IG (dec. CAA)
Aspirin
(Anti-inflammatory, anti-pyretic, anti-platelet)
Possible Reye syndrome- recommend influenza vaccine
Echocardiogram- evaluate for CAA

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16
Q

kawasaki buzz words

A
High-grade Fever for multiple days
Strawberry Tongue
Conjunctivitis
Thrombocytosis and peeling of fingers
Erythematous Maculopapular Rash
Coronary Artery Aneurysms
Treated with Aspirin in Childhood
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17
Q

“gelling phenomenon”

A

joint pain is worse in the morning and after periods of sitting and watching television

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18
Q

ESR vs CRP

A

ESR: concentration of fibrinogen and other inflammatory modulators that have half-lives of days to weeks.
CRP: made exclusively in the liver and can rise and fall within hours of an acute inflammatory stimulus

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19
Q

JIA (Juvenile Idiopathic Arthritis)

20
Q

JIA types

A

polyarthritis
oligoarthritis
systemic: characteristic arthritis that develops with fever and rash; and exclusion of other juvenile arthritis

21
Q

JIA comps

A

Chronic iridocyclitis in pauciarticular JRA (other ocular disease includes iritis, and uveitis)

Joint deformities in polyarticular JRA
(can have positive or negative rheumatoid factor)

22
Q

common tests for GAS (rheumatic fever)

A

throat cx

anti–streptolysin O (ASO) and anti–deoxyribonuclease B (anti–DNAase B)

23
Q

ASO titers

A

peak 3 to 6 weeks after GAS infection.
They are elevated in 80% of patients with typical rheumatic fever (and GABHS pharyngitis)
less than 50% of kicks w/ rec. GABHS skin inf.
less than 70% of patients with chorea

24
Q

Anti–DNAase B titers

A

more reliable, in both pharyn. and skin GABHSpts

peak 6 to 8 weeks after GABHS infection. The elevated titers may persist for several months after infection

25
elevation of ??? in 95% rheumatic fever pts
anti–DNAase B, antistreptokinase, or antihyaluronidase
26
Jones Criteria for rheumatic fever
2 major criteria or 1 major + 2 minor + evidence of recent GAS infection (+ throat cx/RADT, rising ASO titers) MAJOR: carditis, polyarthritis, chorea, erythema marginatum MINOR: fever, arthralgia, elevated APPs, prol. PR interval
27
JIA tx
Hospitalization Cardiology consult PCN or Erythromycin (if patient is allergic to PCN) arthritis and carditis tx: ASA 90 to 120mg/kg/day until symptoms resolve chorea tx: Haloperidol, phenobarbital, or valproic acid
28
JIA ppx
Start prophylactic antibiotics immediately after the therapeutic antibiotic course is completed. Continue until child is an adult and is recurrence free for 10 years (longer if they have residual heart disease) Options for lower risk of recurrent ARF: PCN V K, Sulfadiazine, Macrolides Higher risk of recurrent ARF: Benzathine PCN G intramuscularly, every 4 weeks
29
RF summary
``` Age range: 5-15yo Seasonality: Winter Preceding URI Strep Pharyngitis Jones criteria ```
30
RF: carditis
``` Prolonged PR interval Varying degrees of heart block Cardiomegaly may be noted on CXR Inflammation of valves and endocardium valvular regurgitation/stenosis Mitral valve most common (rheuMATic: Valves affected Mitral>Aortic>Tricuspid) ```
31
RF: skin/ST
(typically only in carditis patients) Subcutaneous nodules over bony prominences present up to a month Erythema marginatum annular erythema, usually present on the trunk and proximal portions of the extremities, sparing the face
32
RF: CNS
Sydenham Chorea abrupt, purposeless, nonrhythmic, involuntary movements that cease during sleep muscular weakness emotional disturbances; ranges from outbursts of inappropriate behavior to transient psychosis Occur 3-8 months after GAS infection
33
RF labs
``` elev. ESR, CRP CXR: mild effusion EKG: prol. PR interval Echo: mitral valve regurg +ASO ```
34
erythema nodosum
type of panniculitis, inflammation of subcutaneous fat in the skin, usually first evident as an outcropping of erythematous nodules that are highly sensitive to touch Most located symmetrically on the ventral aspect of the lower extremities tests: CBC, ESR, ASO titers, Excisional biopsy (when clinical diagnosis is in doubt)
35
Henoch Schonlein Purpura
Small-vessel vasculitis associated with abrupt onset of a rash, palpable purpura most common; GI manifestation, arthritis and arthralgia, and late renal manifestations, commonly after exposure to triggering antigen (eg infectious agent) tests: CBC, ESR, abdominal US, urinalysis, ASO titers, Excisional biopsy (when clinical diagnosis is in doubt)
36
Immune thrombocytopenic purpura
Thrombocytopenia associated with petechia or purpura; bleeding (e.g., gingival, gastrointestinal, mucocutaneous); symptoms of end-organ ischemia (in patients with thrombotic disease) tests: CBC with peripheral smear, coagulation studies, platelet-associated antibody (immunoglobulin G), electrolytes, BUN, creatinine, LDH, urinalysis
37
leukemia
Nonspecific symptoms of fever, easy bleeding, skin findings (e.g., petechiae, purpura), bone pain, fatigue, hepatosplenomegaly, lymphadenopathy tests: CBC, ESR, coagulation profile, bone marrow biopsy
38
meningococcemia
Malaise, fever, rash (e.g., maculopapular rash, petechiae, ecchymosis), and hypotension with possible associated symptoms of meningitis or tenosynovitis tests: CBC, PT/aPTT, fibrinogen, fibrin degradation productions, blood culture, CSF analysis and culture
39
polyarteritis nodosa
Multisystem involvement from segmental inflammatory, necrotizing vasculitis of the small- and medium-sized muscular arteries leading to general symptoms of fever, weakness, weight loss, malaise, myalgia, rash (e.g., livedo reticularis, purpura), headache, and abdominal pain tests: Biopsy of involved organ, urinalysis, CBC, ESR, CRP, angiography
40
RMSF
Headache; fever associated with a centripetal rash (involving palms and soles, spreading to arms, legs, and trunk) that is often petechial; report of recent tick bite or outdoor activity in endemic area tests: Immunofluorescence staining of tissue specimen or serologic analysis for Rickettsia rickettsii, CBC, electrolytes
41
HSP (Henoch Schonlein Purpura/IgA vasculitis)
most common vasculitis in children (about 50% of cases). S/S Hallmark: non-thrombocytopenic palpable purpura. LE and buttocks Colicky abdominal pain (50%) Occult blood (50%) Arthritis(50-67% kiddos) Mainly in knees and ankles ]renal involvement (hematuria) (1/3rd kiddos) screen monthly with UA for 6 months, nephritis is a late finding recent URI (2/3 cases) elevated ASO (50%)
42
HSP dx
triad of purpura, abdominal pain, and arthritis Non-blanching palpable purpura of LE and butt absence of thrombocytopenia Skin biopsy(rare): characteristic IgA deposits in vessel walls Renal biopsy (only indicated if nephritis develops): membranoproliferative glomerulonephritis similar to IgA nephropathy
43
HSP comps
considered benign hosp. if abd pain, GI bleed, intussusception, renal involve - 5% kids-->renal failure - 2-3% intussusception (60% ileoileal) - 33% recurrence rate
44
HSP tx
min: supportive mild: acetomin/NSAIDs mod: corticosteroids sev: cortsters + adj. immunsuppr (cyclophosphamide, IVIG) or plasmapheresis
45
HSP labs
Abdominal CT:marked bowel wall thickening from the vasculitis Abdominal US: identify constipation, intussusception, or other GI involvement ASO titers – Previous strep inf BMP (electrolytes, BUN, Cr) – monitor for renal insufficiency Blood culture – Evaluate for bacteremia or sepsis as possible cause CBC – identify WBC, HCT, Hgb, platelets Anemia could indicate GI bleed Identify thrombocytopenia CRP, ESR – indicate inflammatory reaction IgA levels – typically elevated in HSP, but nonspecific PT/PTT – Elevated levels make bleeding diathesis more probable UA – Assess for renal involvement Serology – Evaluate for cause of infection