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MEASLES
RUBEOLA
OR MORBILLI
Department of infectious disease
WANG JINGYAN
DEFINITION
•
Measles is an acute highly contagious viral
disease caused by measles virus.It is
characterized by fever,URT catarrhal inflamation,
koplik’s spots and maculopapules.
•
The disease may complicated with branchpneumonia, encepholitis, hepatitis.
•
The lived attenuated measles virus
• vaccine has been utilized wildly since 1965 ,the
incidence of the disease has declined in china.
ETIOLOGY
•
1 .Pathogen is measles virus.
it has been classed as a paramyxovirus.it is
spherical in appearance ,measuring about
100~150nm in diameter.It has an outer envelope
composed of M-protein, H-protein, F-protein,
and internal core is RNA.
• 2 .Site of the measles virus exists
measles can be detected from blood and nasal,
pharyngeal secretions.
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•
•
•
•
•
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3. Three kinds of antibodies are produced
after infection,that is
3.1 complement combining antibody;
`
3.2 hemagglutinin inhibiting antibody
3.3 neutralizing antibody
4 .Only one antigenic type of measles virus
is known.
5.Resistance:measles virus is sensitive to
heat or disinfectant , it is also inactivated by
ultraviolet light easily.not strong
EPIDEMIOLOGY
• 1.Source of infection
The patients are the only source of infection.
• 2 .Routes of transmission
air-borne
• 3. Susceptibility of population
3.1 All age person is susceptible; 90% of
contact people acquire the disease.
3.2 The permanent immunity acquire after
disease.
• 4. Epidemic features
season:winter and spiring
age:6 months to 5 years old
PATHOGENESIS AND PATHOLOGY
measles virus
↓respiratory tract
epithelial cells(multiply)
↓lymphoid tissue
blood (first virusemia)
↓
MPS(multiply)
↓
blood (second virusemia)
↓
general toxic symptoms
PATHOLOGY
•
•
•
•
Rash: corium superficial blood vessel
Pigmentation:
Desquamation:
Koplik’s spots
CLINICAL MANIFESTATIONS
• Typical type
• 1.Incubation period is approximately
6~18days,10days is the most common.
(3-4weeks)
• 2 .predromal phase
3~4 days.
2 .1 Fever;
2 .2 Catarrhal inflammation of URT;
2 .3 Koplik’s spots;
2 .4 Transient prodromal rashes.
• 3. Eruption stage
3 .1. Time: the3~5 days after fever;but the 4th
day is most common;
3 .2 . Shape:maculopapular
3.3. Seuence:behind the ear→along the
hairline→face→neck→chest→back→abdome
n→limbs→hand and feet(palm,sole)
3 .4 . The temperature rise continously and
companied with the toxic symptoms
exaggerate
• 4 . Convalescent stage
brown staining.
fine branny desquamation.
course:10-14 days
• Atypical measles
1 . mild measles;
2 . severe measles (toxic and shock type
measles);
3. hemorrhagic measles;
4 . variant measles.
COMPLICATIONS
•
•
•
•
1 .Bronchopneumonia;
2 .Myocarditis;
3 .Laryngitis;
4 .Neurologic complications:
Encephalitis and SSPE .
0.1-0.2%
1-4/m
2-6days
2-17ys
viral encephalitis retrograde change
early-viral
mutation
late crossed immune
LABORATORY FINDINGS
• Blood routine
• Serum Ab measurement
complement combining antibody;
hemagglutinin inhibiting antibody;
neutralizing antibody;
specific antibody IgM.
• Other Ag and multinucleated giant cells
• The separation of virus
DIAGNOSIS
• 1 .Epidemiologic data;
• 2 .Clinical manifestations;
• 3. Laboratory findings:
. 3 .1 .Multinucleated giant cells are
detected in nasopharyax mucosa
secretions;
• 3 .2 .Measles virus can be isolated in
tissues culture;
. 3 .3 . Antibody titer;
• 3 .4 . WBC is relative low .
DIFFERENTIAL DIAGNOSIS
• 1 .Rubella (German measles) ;
• 2 .Roseola infantum (infant
subitum,exanthem subitum)
• 3. Drug rashes.
*the early stage definite diagnosis is:
*the early stage clinical diagnosis is:
*the clinical diagnosis is:
treatment
•
1 .General therapy: rest, nursing and
diet
• 2. Symptomatic therapy: fever and
cough,
• 3.Support threapy:r-globulin
traditional chinese herbs may be
used ;
• 4.complications of treatment
PREVENTION
• 1 .Control source of infection;
• 2 .Interruption of transmissions ;
• 3 .Protection of the susceptible person:
3.1 . Active immunization
Lived attenuated measles vaccine.
plan immune:8m,7j
epidemic stage:before 2 m
contactor:with in 2 days
Contraindications:pregnancy et al
3.2 . Passive immunization
placenta globulin or gamma globulin.
<5 days
prevent onset
>5 days
relieve symptoms
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