Acute intra-familial erythroblastopenia and hereditary spherocytosis: roleof parvovirus B19 infection

Citation
B. Granel et al., Acute intra-familial erythroblastopenia and hereditary spherocytosis: roleof parvovirus B19 infection, REV MED IN, 22(7), 2001, pp. 664-667
Citations number
11
Categorie Soggetti
General & Internal Medicine
Journal title
REVUE DE MEDECINE INTERNE
ISSN journal
02488663 → ACNP
Volume
22
Issue
7
Year of publication
2001
Pages
664 - 667
Database
ISI
SICI code
0248-8663(200107)22:7<664:AIEAHS>2.0.ZU;2-Z
Abstract
Introduction. - Acute parvovirus B19 infection induces a transient inhibiti on of erythroid cell formation, which may induce an erythroblastopenia cris is in patients suffering from chronic hemolytic anemia. Exegesis. - We report here an exceptional observation of acute erythroblast openia crisis with good outcome, occurring at the same time in a mother and her son, both suffering from hereditary spherocytosis. Diagnosis of parvov irus infection is based on detection of serum parvovirus B19-specific immun oglobulin M antibodies in the mother and her son and by the positivity of p arvovirus B19 DNA detected by PCR in serum in the mother. Outcome was good, with the end of the erythroblastopenia crisis obtained 7 to 10 days later, but requiring blood transfusion in the mother. Conclusion. -Our observation is a reminder that the contagiosity of parvovi rus B19 is high in household contacts and that protection of family members should rapidly be considered in hereditary spherocytosis. (C) 2001 Edition s scientifiques et medicales Elsevier SAS.