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Published on: February 17, 2018
Fatal parvovirus myocarditis in a 5-year-old girl
C E Murry1, K R Jerome, D D Reichenbach
1Department of Pathology, University of Washington, Seattle, WA 98195, USA.
Insights
Parvovirus B19 infection, typically mild in children, can lead to fatal myocarditis. This case suggests an autoimmune response, not direct viral infection, may cause severe heart inflammation in parvovirus B19 cases.
Area of Science:
- Cardiology
- Virology
- Immunology
Background:
- Parvovirus B19 infection is common in children, usually causing mild symptoms like erythema infectiosum.
- Fatal outcomes are rare, making severe complications like myocarditis noteworthy.
Observation:
- A 5-year-old girl with diagnosed parvovirus B19 infection died suddenly.
- Autopsy revealed severe myocarditis with significant immune cell infiltration in the heart.
- Extensive testing ruled out other common viral causes of myocarditis.
Findings:
- Quantitative PCR confirmed active parvovirus B19 infection in the patient's blood.
- However, parvovirus B19 DNA was not detected in the heart tissue via immunostaining or PCR.
- Myocardial parvovirus levels were low, consistent with blood content, not direct cardiac infection.
Implications:
- Parvovirus B19 infection can be a trigger for fatal myocarditis in children.
- The mechanism may involve an immune-mediated cross-reaction between viral epitopes and cardiac tissue.
- This highlights the potential for autoimmune complications following common viral infections.
Abstract:
Infection with parvovirus B19 is common in children and typically causes mild illness. We report here the case of a 5-year-old girl who died suddenly, 2 weeks after the clinical diagnosis of a parvoviral infection (erythema infectiosum). Microscopic examination of the heart showed severe myocarditis with extensive T-cell and macrophage infiltration. Cultures, serology, and molecular analyses of serum for enteroviridae, adenovirus, influenza, varicella zoster, cytomegalovirus, and herpes simplex viruses were negative. Quantitative polymerase chain reaction (PCR) analysis for parvovirus B19 in peripheral blood, however, showed active infection (91,000 genomes/mL serum; 2.4 genomes/mononuclear cell). Despite the presence of myocarditis, immunostaining for parvoviral surface antigens was negative in the heart. Quantitative PCR analysis of paraffin sections showed that myocardial parvoviral content was significantly less than that of the normal appearing kidney and within the range predicted simply by tissue blood content. Thus, parvovirus B19 infection can be complicated by fatal myocarditis. Because the virus does not appear to have infected the heart, per se, we speculate that myocarditis arose from immunological cross-reaction to epitopes shared between the virus and the myocardium. HUM PATHOL 32:342-345.
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