Abstract

Since the discovery of parvovirus B19 by Ivonne Cossart 25 years ago, the knowledge of infection due to this virus has evolved from self-limiting erythema infectiosum in immunocompetent children to lethal cytopenia in immunocompromised patients. Now, it is possible to prevent these life-threatening parvovirus B19-mediated diseases [2, 3]. In this issue of Clinical Infectious Diseases, Lindblom et al. [1] comment on how parvovirus B19 infection causes severe cytopenia and can mimic a leukemic relapse or therapy-induced pancytopenia in children with acute lymphoblastic leukemia, causing significantly longer periods without chemotherapy and a higher number of blood transfusions in parvovirus B19 DNA-positive children, compared with parvovirus B19 DNA-negative patients (n = 99). In their cohort of 99 patients, 18 were parvovirus B19 DNA positive at the time of diagnosis or during therapy, and only 1 child was infected after chemotherapy. The number of days of unwanted treatment interruption was significantly higher for parvovirus B19-positive

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