Roseola
Basics
Omnipresent infection occurring in infancy and childhood; majority of cases are caused by human herpesvirus 6 (HHV-6); may be associated with other diseases including encephalitis
Description
- Acute infection of infants or very young children
- Causes a high fever; once fever resolves, skin eruption begins
- Rash is a sudden, pink, maculopapular eruption on starting on the trunk and limbs and spreads distally (1).
- Transmission via contact with salivary secretions or respiratory droplet
- Incubation period of 9 to 10 days
- System(s) affected: skin/exocrine, metabolic, gastrointestinal, respiratory, neurologic
- Synonym(s): roseola infantum, exanthem subitum; pseudorubella; sixth disease; 3-day fever
Pediatric Considerations
A disease of infants and very young children
Epidemiology
- Predominant age
- HHV-6
- Infants and very young children (<2 years old)
- Peak age infection 6 to 9 months, rarely congenital or perinatal infection
- 95% of children have been infected with HHV-6 by 2 years of life.
- HHV-7
- Later childhood
- Mean age of infection 26 months
- >90% population with HHV-7 by 10 years
- HHV-6
- Predominant sex: male = female
- No seasonal variance
Incidence
Common: accounts for 20% ED visits for febrile illness among children 6 to 8 months
Prevalence
- Peak prevalence is between 9 and 21 months.
- Nearly 100% population carrying HHV-6 by 3 years.
- Approximately 20% patients with primary HHV-6 have roseola.
Etiology and Pathophysiology
- HHV-6 and HHV-7
- Majority of cases (60–74%) due to HHV-6
- HHV-6B > HHV-6A
- HHV-6A seen in children in Africa
- HHV-6 binds to CD46 receptors on all nucleated cells.
- Primary infection typically through respiratory droplets or saliva
- Congenital infection/vertical transmission occurs in 1% of cases.
- Transplacental transmission
- Chromosomal integration (clinical significance unknown)
- Lifelong latent or persistent asymptomatic infection occurs after primary infection.
- 80–90% of population intermittently sheds HHV-6/HHV-7 in saliva.
- Patients are viremic from 2 days prior to fever until defervescence and onset of rash.
- HHV-6 latency is also implicated in CSF.
Genetics
HHV-6 is integrated into the chromosomes of 0.2–3% of the population. This leads to vertical transmission of the virus. Clinical significance of this is unknown.
Risk Factors
- Female gender
- Having older siblings
- At-risk adults: immunocompromised
- Renal, liver, other solid organ, and bone marrow transplant (BMT)
- HHV-6 reactivation can occur in first week posttransplant. HHV-6 viremia occurs in 30–45% of BMT within the first several weeks after transplantation.
- Usually asymptomatic
- Up to 82% of HHV-6 reactivation/reinfection in solid organ transplant
- Non-risk factors
- Child care attendance
- Method of delivery
- Breastfeeding (HHV does not appear to pass through breast milk.)
- Maternal age
- Season
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