Severe bone marrow failure associated with human parvovirus B19 infection in a case with no underlying disorder

2012 ◽  
Vol 96 (6) ◽  
pp. 820-821 ◽  
Author(s):  
Chihiro Kawakami ◽  
Yukako Kono ◽  
Akiko Inoue ◽  
Kimitaka Takitani ◽  
Takayuki Ikemoto ◽  
...  
1993 ◽  
Vol 44 (3) ◽  
pp. 207-209 ◽  
Author(s):  
A. Azzi ◽  
R. Fanci ◽  
S. Ciappi ◽  
K. Zakrzewska ◽  
A. Bosi

2003 ◽  
Vol 36 (2) ◽  
pp. 299-302 ◽  
Author(s):  
Sérgio Setúbal ◽  
Maria Cristina Jorge-Pereira ◽  
Anadayr Leite Martins de Sant'Anna ◽  
Solange Artimos de Oliveira ◽  
Anna Ricordi Bazin ◽  
...  

Human parvovirus B19 replicates in erythrocyte precursors. Usually, there are no apparent hematological manifestations. However, in individuals with high erythrocyte turnover, as in patients with sickle-cell disease and in the fetus, the infection may lead to severe transient aplasia and hydrops fetalis, respectively. In AIDS patients, persistent infection may result in chronic anemia. By contrast, in HIV-positive patients without AIDS the infection evolves as a mild exanthematous disease. Two clinical descriptions exemplify these forms of presentation. In the first, an AIDS patient presented with bone marrow failure that responded to immunoglobulin. In the second, an HIV-positive patient without AIDS had a morbilliform rash, and needed no treatment. Knowing that an AIDS patient has chronic B19 anemia lessens concern about drug anemia; protects the patient from invasive diagnostic maneuvers; and prevents the patient from disseminating the infection. In AIDS patients with pure red cell aplasia, a search for parvovirus B19 DNA in the serum or in the bone marrow is warranted.


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