Fifth disease
| Erythema infectiosum | |
|---|---|
 16-month-old with erythema infectiosum | |
| Classification and external resources | |
| Specialty | Infectious disease |
| ICD-10 | B08.3 |
| ICD-9-CM | 057.0 |
| DiseasesDB | 4442 |
| MedlinePlus | 000977 |
| eMedicine | emerg/378 derm/136 ped/192 |
| Patient UK | Fifth disease |
| MeSH | D016731 |
- Not to be confused with sixth disease. See Exanthema subitum.
Erythema infectiosum or fifth disease is one of several possible manifestations of infection by parvovirus B19.[1] The disease is also referred to as slapped cheek syndrome, slapcheek, slap face or slapped face.[2][3]
The name "fifth disease" comes from its place on the standard list of rash-causing childhood diseases, which also includes measles, scarlet fever, and rubella.
Signs and symptoms
Fifth disease starts with a low-grade fever, headache, rash, and cold-like symptoms, such as a runny or stuffy nose. These symptoms pass, then a few days later the rash appears. The bright red rash most commonly appears in the face, particularly the cheeks. This is a defining symptom of the infection in children (hence the name "slapped cheek disease"). Occasionally the rash will extend over the bridge of the nose or around the mouth. In addition to red cheeks, children often develop a red, lacy rash on the rest of the body, with the upper arms, torso, and legs being the most common locations. The rash typically lasts a couple of days and may itch; some cases have been known to last for several weeks. Patients are usually no longer infectious once the rash has appeared.[2][3]
Teenagers and adults may present with a self-limited arthritis. It manifests in painful swelling of the joints that feels similar to arthritis. Older children and adults with fifth disease may have difficulty in walking and in bending joints such as wrists, knees, ankles, fingers, and shoulders.[2][3]
The disease is usually mild,[4] but in certain risk groups it can have serious consequences:
- In pregnant women, infection in the first trimester has been linked to hydrops fetalis, causing spontaneous miscarriage.
- In people with sickle-cell disease or other forms of chronic hemolytic anemia such as hereditary spherocytosis, infection can precipitate an aplastic crisis.[2][3]
- Those who are immuno-compromised (HIV/AIDS, chemotherapy) may be at risk for complications if exposed.[5]
Transmission
Fifth disease is transmitted primarily by respiratory secretions (saliva, mucus, etc.) but can also be spread by contact with infected blood. The incubation period (the time between the initial infection and the onset of symptoms) is usually between 4 and 21 days. Individuals with fifth disease are most infectious before the onset of symptoms. Typically, school children, day-care workers, teachers and parents are most likely to be exposed to the virus. When symptoms are evident, there is little risk of transmission; therefore, symptomatic individuals don't need to be isolated.[2][3]
Treatment
Treatment is supportive as the infection is frequently self-limiting. Antipyretics (i.e., fever reducers) are commonly used. The rash usually does not itch but can be mildly painful. There is no specific therapy.
Epidemiology
Any age may be affected although it is most common in children aged five to fifteen years.[6] By the time adulthood is reached about half the population will have become immune following infection at some time in their past.[2][3] Outbreaks can arise especially in nursery schools, preschools, and elementary schools. Infection is an occupational risk for school and day-care personnel.[7] There is no vaccine available for human parvovirus B19,[3] though attempts have been made to develop one.[8]
History
The name "fifth disease" is not typically capitalized, since the name derives from its historical classification as the fifth of the classical childhood skin rashes or exanthems. Their classification is as follows:
- Measles
- Scarlet fever
- Rubella
- Dukes' disease
- Fifth disease (erythema infectiosum)
- Roseola
It was first described by Robert Willan in 1799 as "Rubeola, sine catarrho". It was better defined by Anton Tschamer in 1889 as a rubella variant ("Ortliche Rotheln"), identified as a distinct condition in 1896 by T. Escherich, and given the name "erythema infectiosum" in 1899.[9]
See also
References
Notes
- ↑ Weir E (March 2005). "Parvovirus B19 infection: fifth disease and more". CMAJ 172 (6): 743. doi:10.1503/cmaj.045293. PMC 552884. PMID 15767606.
- 1 2 3 4 5 6 Sabella C, Goldfarb J; Goldfarb (October 1999). "Parvovirus B19 infections". Am Fam Physician 60 (5): 1455–60. PMID 10524489. Retrieved 2009-11-06.
- 1 2 3 4 5 6 7 Servey JT, Reamy BV, Hodge J; Reamy; Hodge (February 2007). "Clinical presentations of parvovirus B19 infection". Am Fam Physician 75 (3): 373–6. PMID 17304869. Retrieved 2009-11-06.
- ↑ Mankuta D, Bar-Oz B, Koren G; Bar-Oz; Koren (March 1999). "Erythema infectiosum (fifth disease) and pregnancy". Can Fam Physician 45: 603–5. PMC 2328398. PMID 10099795.
- ↑ Yoto, Y., et. al, (2003). "Retrospective study on the influence of human parvovirus B19 infection among children with malignant diseases". Acta Haematol pg.8–12, PMID 8237278
- ↑ Kwon, Kenneth T (March 19, 2009). "Pediatrics, Fifth Disease or Erythema Infectiosum". eMedicine. Retrieved November 7, 2009.
- ↑ Gillespie, S. M.; Cartter, M. L.; Asch, S; Rokos, J. B.; Gary, G. W.; Tsou, C. J.; Hall, D. B.; Anderson, L. J.; Hurwitz, E. S. (1990). "Occupational risk of human parvovirus B19 infection for school and day-care personnel during an outbreak of erythema infectiosum". JAMA 263 (15): 2061–5. doi:10.1001/jama.1990.03440150069028. PMID 2157074.
- ↑ Ballou WR, Reed JL, Noble W, Young NS, Koenig S (2003). "Safety and immunogenicity of a recombinant parvovirus B19 vaccine formulated with MF59C.1". J Infect Dis 187 (4): 675–8. doi:10.1086/368382. PMID 12599085.
- ↑ Altman, Lawrence K (November 30, 1982). "THE DOCTOR'S WORLD". The New York Times. Retrieved November 7, 2009.
External links
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