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8705947
Kawasaki Disease
Description
Mind Map on Kawasaki Disease, created by danny ramos on 27/04/2017.
Mind Map by
danny ramos
, updated more than 1 year ago
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Created by
danny ramos
over 7 years ago
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Resource summary
Kawasaki Disease
DEFINITION
also known as
mucocutaneous lymph node syndrome
is a disease
blood vessels
through the body
become inflamed
EPIDEMIOLOGY
vasculitis
rare in children
incidence
10 and 50 / 100.000
< 5% of referrals to pediatric rheumatologist
2 common types deleted
< 1%
of chronic inflammatory disorders in childhood
2 common types
kawasaki disease
similar %
have evidence of infection
bacterial
viral
systemical
local
predominant children
< 2 years
rare in late childhood
henoch schonlein (HSP)
1/3 of cases HSP
after Streptococcal infection
posible pathogenesis
suggest a close connection
transmisible agent
occurs regularly in 1980
average of patients
age decreased
% of girls increased
decades of attempts to prove
viruses
bacterial toxins
specific pathogens
causes most cases
not been subestimated
RISK FACTOR
most type of vasculitis
not known
rick factors are equally hidden
infections
inmunization
genetic factors
inmunomoduladory
haplotypic
vascular genes
do not explain phenomena
monogenic diseases
vasculopathy
associted with
mutations in adenosine deaminase 2
PATHOPHYSIOLOGY
pathology characteristics
primary target of inflammation
medium-sized muscular arteries
coronary arteries
most affected
most likely to suffer
chronic damage
neutrophils
invade
vessels walls
neutrophil infiltrate
evident in the arterial wall
first 2 week of disease
immunologic response
gene expression studies
DNA microarrays
from acute - phase whole blood
confirm increased relative abundance with neutrophils
adrenomodulin
grancalcin
granulin
decreased NK
decreased CD8 + lymphocytes
CLINICAL FEATURES
differ from chronic vaasculophaties
characteristics of any type of vasculitis
fever
malaise
fatigue
failure to thrive
increased levels
acute - phase reactant
progressions immits viral infections
rash
eritema
desquamation
mucosal inflammation
extremity changes
non - exudative conjuntivitis
cracked
red lips
strawberry tongue
beau lines (nails)
arthritis
commonly affects
lower extremities
small joint polyarthritis
cervical lymphoadenopaty
LABORATORY FINDINGS
systemic inflammation
PCR
erytrocyte sedimentation rate
Alpha 1 antitripsine
leukocytosis
increased platelets levels
normonytic,normochromic anemia
Hb concentration
more than 2 DE
urianalysis
white blood cells
liver enzymes
increased transminase levels
mild hyperbilirrubinemia
obstructive jaundice
from hydrops of gallbladder
cerebrospinal fluid
pleocythosis
DIFFERENTIAL DIAGNOTICS
mucocutaneos inflammation
measles
echovirus
adenovirus
toxin mediated illness
mediated by B - hemolytic streptococcus
rocky mountain fever and leptospirosis
steven - johnson syndrome
drug reaction
mercury hipersensitive reaction
PAN
rheumatoid arthritis
MANAGMENT
IVIG
for 10 days
reduces incidence of
coronary artery aneurysm
by more than 70%
aspirin
antiinflammatory and antithrombotic effects
initial dose 100 mg/kg/d
once fever is solved
3 to 5 mg/kg/d
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