Wednesday, March 28, 2012
Measles
* an acute viral infection characterized by a maculopapular
rash erupting successively over the neck, face, body, and extremitis and
accompanied by a high fever.
ETIOLOGY
Measles virus
*An
RNA virus of the genus Morbillivirus in the family of Paramyxoviridae
*One
serotype, human’s only host
*Stable antigenicity
*Rapidly
inactivated by heat and light
*Survival
in low temperature.
EPIDEMIOLOGY
*Infection
sources
n Patients
of acute stage and viral carriers of
atypical measles
*Transmission
n Highly
contagious, approximately 90% of susceptible contacts acquire the disease.
n Respiratory
secretions: maximal
dissemination of virus occurs by droplet spray during the prodromal period
(catarrhal stage).
n Contagious
from 5 days before symptoms, 5 days after onset of rash
n Seasons:
in the spring, peak in Feb-May
PATHOGENESIS AND PATHOLOGY
*Portal
of entry
n Respiratory
tract and regional lymph nodes
n Enters
bloodstream (primary viraemia) è monocyte – phagocyte system è
target organs (secondary viraemia)
*Target
organs
n The
skin; the mucous membranes of the nasopharynx,
bronchi, and intestinal tract; and in
the conjunctivae, ect
Resulting
In-----
1)
Koplik spots and skin rash: serous exudation and proliferation
of endothelial cells around the capillaries
2)
Conjunctivis
PATHOGENESIS AND PATHOLOGY
3) Laryngitis, croup,
bronchitis :general inflammatory reaction
4)
Hyperplasia of lymphoid tissue: multinucleated
giant cells (Warthin-Finkeldey giant
cells) may be found
5)
Interstitial pneumonitis: Hecht
giant cell pneumonia.
6)
Bronchopneumonia: due to secondary bacterial infections
7)
Encephalomyelitis: perivascular
demyelinization occurs in areas of the brain and spinal cord.
8)
Subacute sclerosing panencephalitis(SSPE):
degeneration of
the cortex and white matter with intranuclear and intracytoplasmic inclusion
bodies
CLINICAL MANIFESTATION
Typical
Manifestation:
patients havn’t
had measles immunization, or vaccine failure with normal immunity or those
havn’t used immune globulin
1.
Incubation period (infection to symptoms) :
6-18days (average 10 days)
2.
Prodromal period:
n 3-4
days
n Non-specific
symptoms: fever, malaise, anorexia, headache
n Classical
triad: cough, coryza, conjunctivitis (with
photophobia, lacrimation)
CLINICAL MANIFESTATION
Enanthem (Koplik spots):
n Pathognomonic
for measles
n 24-48
hr before rash appears
n 1mm, grayish white dots with
slight, reddish areolae
n Buccal mucosa, opposite the
lower 2nd molars
n increase
within 1day and spread
n fade
soon after rash onset
CLINICAL MANIFESTATION
CLINICAL MANIFESTATION
3. Rash period
3-4days
Exanthem:
Erythematous, non-pruritic,
maculopapular
n Upper lateral of the neck, behind ears,
hairline,
face è
trunk arms and legs feet
n The severity of the disease is directly
related to
the extent and confluence of the rash
,
CLINICAL MANIFESTATION
CLINICAL MANIFESTATION
CLINICAL MANIFESTATION
CLINICAL MANIFESTATION
Temperature:
n Rises abruptly as the rash appears
n Reaches 40℃ or higher
n Settles after 4-5 days – if persists,
suspect secondary
infection
Coryza, fever, and
cough:
n Increasingly severe up to the time the rash
has covered the
body
Lymphadenopathy
(posterior cervical region, mesenteric) splenomegaly, diarrhoea, vomiting
Chest X ray:
n May be abnormal,
even in uncomplicated cases
CLINICAL MANIFESTATION
4. Recovery period
3-4days
Exanthem:
n Fades in order of appearance
n Branny desquamation and brownish
discoloration
Entire illness – 10 days
CLINICAL MANIFESTATION
CLINICAL MANIFESTATION
Atypical Manifestation:
1. Mild measles
n In
patients: administered immune globulin products during the incubation period
and immunized against measles; in infants <8mo
n Long
incubation period and short prodromal
phase
n Mild
symptom
n No
Koplik spot
n The
rash tends to be faint, less macular, pinpoint
n No
branny desquamation and brownish discoloration
occur as the rash fades
n No
complications and short course
CLINICAL MANIFESTATION
2.
Severe measles:
n In cases with
malnutrition, hypoimmunity and secondary
infection
n Persistent
hyperpyrexia, sometimes with convulsions and even
coma
Exanthem:
n Completely covered the skin
n Confluent, petechiae, ecchymoses
n The hemorrhagic type of measles (black
measles), bleeding
may occur from the mouth, nose, or
bowel. disseminated
intravascular coagulation (DIC)
CLINICAL MANIFESTATION
CLINICAL MANIFESTATION
3.
Atypical measles syndroma:
n Recipients
of killed measles virus vaccine, who later come in
contact with wild-type measles virus.
n Distinguished by high fever, severe headache,
severe abdominal
pain, often with vomiting, myalgias,
respiratory symptoms,
pneumonia with pleural effusion
Exanthem:
n First appears on the palms, wrists, soles,
and ankles, and
progresses in a centripetal direction.
n Maculopapular è
vesicular è purpuric or hemorrhagic.
n Koplik spots
rarely appear
CLINICAL MANIFESTATION
CLINICAL MANIFESTATION
4.
Measles absent of rush
n Immunodepressed, or passive immunized
recently cases and
occasionally in infants <9mo who have
appreciable levels
of maternal antibody
n Non-specificity
n Difficult to diagnosis
COMPLICATIONS
1.
Respiratory Tract
* Laryngitis,
tracheitis, bronchitis – due to measles itself
* Laryngotrachobronchitis
(croup) –cause airway obstruction to require tracheostomy
* Secondary
pneumonia – immunocompromised, malnourished patients. pneumococcus, group A
Streptococcus, Staphylococcus aureus and
Haemophilus influenzae type B.
* Exacerbation
of TB
COMPLICATIONS
2. Myocarditis
3. Malnutrition and Vitamin A deficiency
COMPLICATIONS
4.
CNS
*The
incidence of encephalomyelitis is 1-2/l,000 cases of measles
*Onset
occurs 2-5 days after the appearance of the rash
*No
correlation between the severity of the rash illness and
that of the neurologic involvement
n Earlier - direct viral effect in CNS
n Later – immune response causing demyelination
n Significant morbidity, permanent sequelae –
mental
retardation and paralysis
*Subacute
sclerosing panencephalitis (SSPE): extremely rare, 6-10 years after infection.
Progressive dementia, fatal. Interaction of host with defective form of virus
LABORATORY
EXAMINATION
*Isolation
of measles virus from a clinical specimen (e.g., nasopharynx, urine)
*Significant
rise in measles IgG by any standard serologic assay
*Positive
serologic test for measles IgM antibody
*Immunofluorescence
detects Measles antigens
*Multinucleated
giant cells in smears of nasal mucosa
*Low
white blood cell count and a relative lymphocytosis in PB
*Measles
encephalitis – raised protein, lymphocytes in CSF
DIAGNOSIS
characteristic
clinical picture:
Measles contact
Koplik spot
Features of the skin rash
The relation between the eruption and fever
Laboratory confirmation is rarely needed
DIFFERENTIAL DIAGNOSIS
*The rash of measles must be differentiated from
that of
*rubella;
*roseola
intantum;
*enteroviral infections;
*scarlet
fever;
*and
drug rashes.
DIFFERENTIAL DIAGNOSIS
DIFFERENTIAL DIAGNOSIS
TREATMENT
*Supportive, symptom-directed
Antipyretics for fever
Bed rest
Adequate fluid intake
Be protected from exposure to strong
light
*Antibiotics for otitis media, pneumonia
*High doses Vitamin A in severe/ potentially severe
measles/ patients less than 2 years
100,000IU—200,000IU
PREVENTION
*1. Quarantine period
5 days after rash
appears, longer for complicated measles
*2. Vaccine
The initial
measles immunization is recommended at 8mo of
age
A second immunization is recommended
routinely at 7yr of
age
*3. Postexposure Prophylaxis
Passive
immunization with immune globulin (0.25mL/kg)
is effective for
prevention and attenuation of measles within
5 days of exposure.
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