Chicken pox
Etiopathogenesis
• Highly infectious disease
• By varicella-zoster virus
• Enveloped DNA virus
• Transmission by direct contact, droplet ,
airborne or fomites.
• Only 1 serotype known
• Man is the only reservoir
• Virus  upper respiratory tract and tonsillar
tissue replicates there for initial 8-10 days
primary viremia into reticuloendothelial
systemsecondary viremia
• Skin lesions seen during the secondary viremia
that lasts for 3-7 days.
• Virus is carried to vescicular fluid and respiratory
tract  shedding  transmits infection to
susceptible contacts
• Virus may be transported to the dorsal nerve
root of spinal cord where latent infection is
established which can be reactivated later to
cause disease.
Clinical features
• Incubation period is 14-16 days
• Diseases starts with fever, malaise, sore throat,
headache.
• Maculopapular rash on 1st day of fever.
• Period of Infectivity from 2 days prior to
appearance of rash upto 3-7 days after the rash.
• Rash begins as crops of macules which evolve into
papules then vesicles with centripetal distribution.
• Vesicles are initially filled with clear fluid then it
becomes cloudy.
• Vesicles persists for 3-4 days  pustules  crusts
 scab  falls in 10-20 days  usually no
permanent scar
• Infectivity is maximum in prodormal phase and
wanes once the lesions are crusted as crusts donot
contain live virus.
• Vesicles may be round, oval or irregular with
surrouned red area.
• Rash 1st on face & scalp  trunk  whole body
• Palms and soles are spared.
• Size of rash 5-10 mm
• Lesions of different stages are seen
simultaneously.
Complications
• Bacterial infections  cellulitis, skin abscess
Pneumonia , Septic arthritis, Osteomyelitis
• Neurological  seen at end of 1st week
- Commonest pure cerebellar ataxia
excellent prognosis
- Encephalitis
- ADEM
- Transverse myelitis, GBS , Seizures
• Varicella pneumonitis  appears 3-5 days after
rash
others
• Myocarditis, Pericarditis , endocarditis
• Hepatitis
• AGN
• Appendicitis
• Keratoconjuctivitis
• Thrombocytopenia
Congenital varicella
• Mother has chickenpox in 1st trimester there is 2%
risk of the baby to develop congenital varicella
embryopathy.
• Malformations includes limb hypoplasia, scarring
of limbs , digital defect , cortical atrophy ,retinitis,
cataract
Varicella neonatorum
• If maternal rash appers 5 days before to 2 days
after the delivery there is 20-30 % chance the
baby will be infected and have chickenpox.
• Very high risk of disseminated disease with death
• Fatality rate is around 30 %
• Baby should receive VZIG & IV acyclovir
Treatment
• Supportive
• Antipyretic  paracetamol no aspirin
• For pruritus  calamine lotion , antihistaminic
• No antiviral for uncomplicated cases
• Acyclovir for complicated cases
• Antibiotics for secondary bacterial infection
Prevention
• Immunization with live vaccine
• 1st dose at 15 months
• 2nd dose at 4-6 years.
• Infection gives life long immunity
MUMPS
Etiopathogenesis
• Mumps is a acute viral infection of the parotid
and other salivary gland.
• Self limiting and vaccine preventable disease
• Mumps a RNA virus belongs to paramyxovirus
group
• Annual incidence is 100-1000 per 1 lakh
population.
• Man is the only host
• Transmission by droplets
• Infective period is 2 days before to 5 days after
the parotitis
• Mumps in adult is severe
• Mumps in pregnancy can lead to abortion
Clinical features
• Incubation period is 16-18 days
• Initial symptoms fever, malaise , headache ,
vomiting,
• Classical symptom is parotitis with enlarged
parotid gland.
• Bilateral in 70 % cases , unilateral in 30 % cases
• 10 % cases other salivary glands are involved
• Associated with difficultly in swallowing ,
chewing, pain in ear, local edema.
• 1st one side then spreads to other side with in
72 hours.
• Swelling increases in size for 3 – 4 days then
starts receding and disappear by 10-14 days.
Complications
• Aseptic meningitis  commonest , in 10 % cases
• Orchitis 25 % in adolescent
• Epididymitis, Oophoritis
• Meningoencephalitis
• Pancreatitis
• Nephritis
• Arthritis
• Thyroditis
• Thromocytopenic purpura
DIAGNOSIS
• Mostly clinical
• Virus can be isolated from nasopharangeal swab,
urine, blood , resp secretions .
• Mumps specific IgG Antibodies
• PCR to detect viral antigen
Treatment
• No specific treatment
• Supportive management
Prevention
• Immunization
THANK U

Chicken pox, measles

  • 1.
  • 2.
    Etiopathogenesis • Highly infectiousdisease • By varicella-zoster virus • Enveloped DNA virus • Transmission by direct contact, droplet , airborne or fomites.
  • 3.
    • Only 1serotype known • Man is the only reservoir • Virus  upper respiratory tract and tonsillar tissue replicates there for initial 8-10 days primary viremia into reticuloendothelial systemsecondary viremia • Skin lesions seen during the secondary viremia that lasts for 3-7 days.
  • 4.
    • Virus iscarried to vescicular fluid and respiratory tract  shedding  transmits infection to susceptible contacts • Virus may be transported to the dorsal nerve root of spinal cord where latent infection is established which can be reactivated later to cause disease.
  • 5.
    Clinical features • Incubationperiod is 14-16 days • Diseases starts with fever, malaise, sore throat, headache. • Maculopapular rash on 1st day of fever. • Period of Infectivity from 2 days prior to appearance of rash upto 3-7 days after the rash.
  • 6.
    • Rash beginsas crops of macules which evolve into papules then vesicles with centripetal distribution. • Vesicles are initially filled with clear fluid then it becomes cloudy. • Vesicles persists for 3-4 days  pustules  crusts  scab  falls in 10-20 days  usually no permanent scar • Infectivity is maximum in prodormal phase and wanes once the lesions are crusted as crusts donot contain live virus.
  • 7.
    • Vesicles maybe round, oval or irregular with surrouned red area. • Rash 1st on face & scalp  trunk  whole body • Palms and soles are spared. • Size of rash 5-10 mm • Lesions of different stages are seen simultaneously.
  • 8.
    Complications • Bacterial infections cellulitis, skin abscess Pneumonia , Septic arthritis, Osteomyelitis • Neurological  seen at end of 1st week - Commonest pure cerebellar ataxia excellent prognosis - Encephalitis - ADEM - Transverse myelitis, GBS , Seizures
  • 9.
    • Varicella pneumonitis appears 3-5 days after rash others • Myocarditis, Pericarditis , endocarditis • Hepatitis • AGN • Appendicitis • Keratoconjuctivitis • Thrombocytopenia
  • 10.
    Congenital varicella • Motherhas chickenpox in 1st trimester there is 2% risk of the baby to develop congenital varicella embryopathy. • Malformations includes limb hypoplasia, scarring of limbs , digital defect , cortical atrophy ,retinitis, cataract
  • 11.
    Varicella neonatorum • Ifmaternal rash appers 5 days before to 2 days after the delivery there is 20-30 % chance the baby will be infected and have chickenpox. • Very high risk of disseminated disease with death • Fatality rate is around 30 % • Baby should receive VZIG & IV acyclovir
  • 12.
    Treatment • Supportive • Antipyretic paracetamol no aspirin • For pruritus  calamine lotion , antihistaminic • No antiviral for uncomplicated cases • Acyclovir for complicated cases • Antibiotics for secondary bacterial infection
  • 13.
    Prevention • Immunization withlive vaccine • 1st dose at 15 months • 2nd dose at 4-6 years. • Infection gives life long immunity
  • 14.
  • 15.
    Etiopathogenesis • Mumps isa acute viral infection of the parotid and other salivary gland. • Self limiting and vaccine preventable disease • Mumps a RNA virus belongs to paramyxovirus group • Annual incidence is 100-1000 per 1 lakh population.
  • 16.
    • Man isthe only host • Transmission by droplets • Infective period is 2 days before to 5 days after the parotitis • Mumps in adult is severe • Mumps in pregnancy can lead to abortion
  • 17.
    Clinical features • Incubationperiod is 16-18 days • Initial symptoms fever, malaise , headache , vomiting, • Classical symptom is parotitis with enlarged parotid gland. • Bilateral in 70 % cases , unilateral in 30 % cases • 10 % cases other salivary glands are involved
  • 18.
    • Associated withdifficultly in swallowing , chewing, pain in ear, local edema. • 1st one side then spreads to other side with in 72 hours. • Swelling increases in size for 3 – 4 days then starts receding and disappear by 10-14 days.
  • 19.
    Complications • Aseptic meningitis commonest , in 10 % cases • Orchitis 25 % in adolescent • Epididymitis, Oophoritis • Meningoencephalitis • Pancreatitis • Nephritis • Arthritis • Thyroditis • Thromocytopenic purpura
  • 20.
    DIAGNOSIS • Mostly clinical •Virus can be isolated from nasopharangeal swab, urine, blood , resp secretions . • Mumps specific IgG Antibodies • PCR to detect viral antigen
  • 21.
    Treatment • No specifictreatment • Supportive management
  • 22.
  • 23.