Observations on human parvovirus B19 infection diagnosed in 2011

2012 ◽  
Vol 153 (49) ◽  
pp. 1948-1957 ◽  
Author(s):  
Ilona Mihály ◽  
András Trethon ◽  
Zsuzsanna Arányi ◽  
Adrienne Lukács ◽  
Tímea Kolozsi ◽  
...  

Introduction: The incidence of human parvovirus B19 infection is unknown. Aim: A retrospective analysis of clinical and laboratory findings was carried out in patients diagnosed with human parvovirus B19 infection in 2011 in a virologic laboratory of a single centre in Hungary. Methods: Clinical and laboratory data of patients with proven human parvovirus B19 infection were analysed using in- and out-patient files. Results: In 2011, 72 patients proved to have human parvovirus B19 infection with the use of enzyme immunoassay. The clinical diagnoses of these patients were as follows: human parvovirus B19 infection (30.6%), transient aplastic crisis (16.7%), arthritis (8.3%) and acute hepatitis (4.1%). Symptoms of each of the four phases of the infection occurred in various combinations with the exception of the monophase of cheek exanthema. This occurred without the presence of other symptoms in some cases. Leading symptoms and signs were exanthema (in 74.6% of cases), haematological disorders (in 69% of cases), fever (in 54.9% of cases) and arthritis (in 33.8% of cases). Several atypical dermatological symptoms were also observed. Acute arthritis without exanthema was noted in 8 patients. Of the 72 patients with proven human parvovirus B19 infection there were 7 pregnant women, and one of them had hydrops foetalis resulting spontaneous abortion. In 16 patients (22.5%) human parvovirus B19 IgG was undetectable despite an optimal time for testing. Conclusion: The observations of this study may contribute to a better recognition of clinical symptoms of human parvovirus B19 infection. Orv. Hetil., 2012, 153, 1948–1957.

1992 ◽  
Vol 34 (5) ◽  
pp. 479-482 ◽  
Author(s):  
R. C. N. Cubel ◽  
M. C. Valadão ◽  
W. V. Pereira ◽  
M. C. Magalhães ◽  
J. P. Nascimento

Specific anti-B19 IgM was demonstrated in sera from three children showing transient aplastic crisis. A two years-old boy living in Rio de Janeiro suffering from sickle-cell anaemia showed the crisis during August, 1990. Two siblings living in Santa Maria, RS, developed aplastic crisis during May, 1991, when they were also diagnosed for hereditary spherocytosis. For a third child from this same family, who first developed aplastic crisis no IgM anti-B19 was detected in her sera.


2009 ◽  
Vol 40 (7) ◽  
pp. 612-617 ◽  
Author(s):  
Shih-Chi Liu ◽  
Chia-Ti Tsai ◽  
Cho-Kai Wu ◽  
Meng-Fen Yu ◽  
Mu-Zon Wu ◽  
...  

The Lancet ◽  
2001 ◽  
Vol 357 (9267) ◽  
pp. 1494-1497 ◽  
Author(s):  
Thomas Tolfvenstam ◽  
Nikos Papadogiannakis ◽  
Oscar Norbeck ◽  
Karin Petersson ◽  
Kristina Broliden

2004 ◽  
Vol 24 (7) ◽  
pp. 513-518 ◽  
Author(s):  
Martin Enders ◽  
Andrea Weidner ◽  
Iris Zoellner ◽  
Karen Searle ◽  
Gisela Enders

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