CASE REPORT article
Front. Pediatr.
Sec. Pediatric Cardiology
Volume 13 - 2025 | doi: 10.3389/fped.2025.1579212
Case Series: Full Recovery in Severe ParvoB19 Myocarditis with DCM Phenotype: The Impact of rASD Creation and Pulmonary Banding
Provisionally accepted- 1Department of Pediatric Cardiology, Faculty of Medicine, University of Giessen, Giessen, Germany
- 2Cardiopathology, Institute for PAthology and Neuropathology, University Tuebingen, Tuebingen, Germany
- 3University Hospital Frankfurt, Frankfurt, Hesse, Germany
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Background: The incidence of parvovirus B19 (B19V)-associated myocarditis progressing to dilated cardiomyopathy (DCM) is on the rise. We hypothesize that a comprehensive treatment regimen enables cardiac regeneration in young patients with life-threatening B19V myocarditis.Methods: Four patients with clinical and imaging evidence of DCM were referred due to suspected myocarditis. An endomyocardial biopsy (EMB) confirmed the diagnosis. The diastolic dysfunction associated with heart failure and reduced left ventricular ejection fraction (HFrEF) was established invasively. Before surgical pulmonary artery banding (PAB), a transcatheter procedure was performed to create a restrictive atrial defect (rASD).Results: The drug-treated patients (ages 15 to 26 months) had a mean LV-EF of 22.5% (20-25%), a left ventricular end-diastolic diameter (LVEDD) of 49 (45-51) mm (Z-score >5), and elevated LVED pressures (>18 mmHg). EMB revealed B19V-associated acute/subacute or chronic active myocarditis with characteristics of DCM. Drug therapy, including immunoglobulins and creating a rASD, resulted in clinical improvement and enhanced right ventricular function. However, LV enlargement and dysfunction persisted. Four weeks after surgical PAB, all patients showed improvement and were discharged home. The pressure gradient across the PAB ranged from 40 to 45 mmHg, and LVEDD decreased to a mean z-score of +3.5. Within three to six months, LVEDD normalized, and LV-EF increased to a mean of 63% (range: 57-68%). Clinical and cardiac improvements were sustained over a median follow-up of 7.5 years.A holistic treatment approach allows functional regeneration in B19V myocarditis with obvious end-stage DCM. Restrictive ASD creation is required before surgical PAB when HFpEF is associated with a diastolic dysfunction component.
Keywords: B19V, Myocarditis, dilated cardiomyopathy, restrictive ASD, Pulmonary Artery Banding (PAB), case report
Received: 18 Feb 2025; Accepted: 14 May 2025.
Copyright: © 2025 Logeswaran, Akintuerk, Mueller, Rueblinger, Gummel, Klingel, Steinbrenner, Jux and Schranz. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Thushiha Logeswaran, Department of Pediatric Cardiology, Faculty of Medicine, University of Giessen, Giessen, Germany
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