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Published on: September 7, 2022
Parvovirus B19 infection in children with a variety of hematological disorders
Maysaa El Sayed Zaki1, Samir AbouEl Hassan, Tarek Seleim
1Clinical Pathology, Faculty of Medicine, Mansoura University, Mansoura, Egypt. may_s65@hotmail.com
Insights
Parvovirus B19 (PB19) infection is common in children with hematological disorders, impacting blood counts. Early screening for PB19 is crucial for accurate diagnosis and management in these pediatric patients.
Area of Science:
- Pediatric Hematology
- Viral Infections
- Immunology
Background:
- Parvovirus B19 (PB19) is a known pathogen affecting red blood cells.
- Its role in pediatric hematological disorders requires further elucidation.
- Understanding PB19's contribution to hematological changes is critical for patient management.
Purpose of the Study:
- To detect Parvovirus B19 (PB19) DNA and antibodies in children with hematological disorders.
- To assess the impact of PB19 infection on hematological parameters.
- To clarify the diagnostic utility of virological markers in this population.
Main Methods:
- Sera from 85 pediatric patients with hematological disorders and 20 healthy controls were analyzed.
- PB19-specific IgG, IgM antibodies, and viral DNA (by PCR) were quantified.
- Patients were categorized into groups based on diagnosis: aplastic crisis, hemolytic anemia, acute leukemia under chemotherapy, and newly diagnosed acute leukemia.
Main Results:
- Significant differences in hemoglobin and RBC counts, neutropenia, and lymphocytosis were observed in PB19-positive patients compared to controls.
- Prevalence of PB19 IgM, IgG, and PCR varied across patient groups.
- IgG was most prevalent in hemolytic anemia groups, while IgM and PCR were higher in acute leukemia under chemotherapy.
Conclusions:
- Parvovirus B19 infection is prevalent in children with hematological disorders.
- PB19 should be suspected in pediatric patients presenting with anemia, neutropenia, and lymphocytosis.
- Combined serological and molecular testing (PCR) is recommended for reliable PB19 diagnosis in these children.
Abstract:
This study was carried out to detect Parvovirus B19 (PB19) DNA together with its antibodies in the sera of children with a range of hematological disorders to clarify the contribution of this infection to changes observed in hematological picture in those populations. This study included 85 pediatric patients with different hematological disorders. Twenty healthy subjects with matched age and sex were included as controls. Patients were classified into four groups; group I included 25 patients with hemolytic anemia in aplastic crisis, group II included 20 patients with hemolytic anemia without aplastic crisis, group III included 20 acute leukemia patients under chemotherapy, group IV included 20 patients with recently diagnosed acute leukemia. Virological study for PB19 included determination of specific IgG & IgM together with viral DNA by polymerase chain reaction (PCR). In all groups of patients with positive markers for PB19, there were statistically significant differences in the mean Hb concentration and RBC count (P < 0.001 for each), presence of neutropenia (P = 0.003) and lymphocytosis (P < 0.001) compared to controls. There was statistically significant difference in the prevalence of PB19 IgM, IgG and PCR among studied groups compared to control group. In group I and group II IgG had the highest positive rate (56 and 35%, respectively). In group III IgG also had a high positive rate (45%). However, in group IV IgM had the highest positive rate (50%) followed by PCR (45%) then IgG (40%). In conclusion, PB19 infection is detected in high rates among children with hematological disorders. PB19 must be suspected and screened for when there is anemia in those patients associated with neutropenia and lymphocytosis. In patients with acute leukaemia under chemotherapy who have unexpected anemia, neutropenia and lymphocytosis Parvovirus infection should be considered before a change of chemotherapy protocol. Screening of blood for PB19 may be helpful in understanding the epidemiology of infection with this virus. The direct detection of DNA by PCR in sera needs to be coupled with serology for a more reliable diagnosis of PB19 infections in these children.
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