| Literature DB >> 25920561 |
Alice Wolfromm1, Christophe Rodriguez2,3, Marc Michel4, Anoosha Habibi5, Vincent Audard3,6, Emmanuel Benayoun1, Olivier Rogier2, Dominique Challine2, Olivier Chosidow7,8,9, Jean-Daniel Lelièvre3,10, Xavier Chevalier11, Fabien Le Bras12, Cécile Pautas13, Michèle Imbert1, Jean-Michel Pawlotsky2,3, Orianne Wagner-Ballon1,3.
Abstract
The virological diagnosis of Parvovirus B19 (PvB19) infection is currently based on sero-diagnosis, molecular methods or both, yet without clear recommendations. We retrospectively identified patients with polymerase chain reaction-positive PvB19 and/or positive serological assay between 2007 and 2013. Eighty-two adults with at least one diagnostic criterion of recent PvB19 infection (IgM antibodies, viral DNA in blood and/or in marrow) were included and classified into three homogeneous groups: 30 patients had no underlying predisposing condition, 25 a hereditary haemolytic anaemia, 27 an underlying immunodeficiency. The classical PvB19-related manifestations were less frequent in immunocompromised than in immunocompetent patients (arthromyalgia: 5 vs. 14; erythema: 4 vs. 17, respectively). Only 41·4% of patients with no underlying disease were anaemic. Bicytopenia and pancytopenia were observed mainly in immunocompromised patients. Classical pure red cell aplasia was observed in only 9 of the 27 marrow smears performed. Specific IgM were found in 93% of immunocompetent patients, whereas only 58% had detectable viral DNA in blood. IgM and DNA were present alone or together in all patients with hereditary haemolytic anaemia. In immunocompromised patients, the diagnosis was confirmed by marrow analysis in 91% of cases. We make some proposals based on this large series of PvB19-infected patients.Entities:
Keywords: anaemia; human parvovirus B19; pure red cell aplasia; underlying predisposing condition
Mesh:
Year: 2015 PMID: 25920561 DOI: 10.1111/bjh.13421
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998