Abstract
The records of 22 children with parvovirus B19-induced aplastic crisis were reviewed. The group consisted of 16 children with sickle cell hemoglobinopathies and 6 with hereditary spherocytosis. Children presented to the hospital 0.5 to 8 days (mean, 2.4 days) after the onset of symptoms. The children with sickle-cell disease presented earlier (mean, 1.4 days) than did children with hereditary spherocytosis (mean, 5 days; P = 0.02. Fever was the most common symptom, occurring in 73% of children. Rash did not occur in either group. Reticulocyte counts began to rise 1 week after onset of illness associated with a rise in parvovirus B19-specific IgG antibody. These data suggest that parvovirus B19 infection in children with sickle-cell hemoglobinopathies and heredity spherocytosis differs from infection in normal children.
| Original language | English |
|---|---|
| Pages (from-to) | 1100-1101 |
| Number of pages | 2 |
| Journal | Pediatric Infectious Disease Journal |
| Volume | 22 |
| Issue number | 12 |
| DOIs | |
| State | Published - Dec 2003 |
Keywords
- Aplastic crisis
- Hemolytic anemia
- Hereditary spherocytosis
- Parvovirus B19
- Sickle-cell anemia
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