Respiratory syncytial virus-associated mortality in a healthy 3-year-old child: a case report

被引:3
|
作者
Gavotto, A. [1 ,2 ]
Ousselin, A. [3 ]
Pidoux, O. [3 ]
Cathala, P. [4 ]
Costes-Martineau, V [5 ]
Riviere, B. [5 ]
Pasquie, J. L. [6 ]
Amedro, P. [1 ,2 ]
Rambaud, C. [7 ]
Cambonie, G. [3 ]
机构
[1] Montpellier Univ Hosp Ctr, Arnaud de Villeneuve Hosp, Pediat & Congenital Cardiol Dept, Montpellier, France
[2] Univ Montpellier, INSERM, UMR 9214, CNRS,U1046, Montpellier, France
[3] Montpellier Univ Hosp Ctr, Arnaud de Villeneuve Hosp, Dept Neonatal Med & Pediat Intens Care, 371 Ave Doyen Gaston Giraud, F-34295 Montpellier 5, France
[4] Montpellier Univ Hosp Ctr, Lapeyronie Hosp, Dept Forens Med, Montpellier, France
[5] Montpellier Univ Hosp Ctr, Lapeyronie Hosp, Dept Pathol, Montpellier, France
[6] Montpellier Univ Hosp Ctr, Arnaud de Villeneuve Hosp, Dept Cardiol, Montpellier, France
[7] Garches Univ Hosp, Raymond Poincare Hosp, Dept Pathol & Forens Med, Garches, France
关键词
Sudden unexpected death in childhood; Respiratory syncytial virus; Myoepicarditis; Cardioneuropathy; Myosin light chain 2; SUDDEN UNEXPECTED DEATH; COMPLETE HEART-BLOCK; HYPERTROPHIC CARDIOMYOPATHY; PERICARDIAL-EFFUSION; INFECTIONS; INFANTS; DISEASE; TAMPONADE; NEED;
D O I
10.1186/s12887-019-1847-2
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundRespiratory syncytial virus (RSV) is the most frequently identified pathogen in children with acute lower respiratory tract infection. Fatal cases have mainly been reported during the first 6months of life or in the presence of comorbidity.Case presentationA 47-month-old girl was admitted to the pediatric intensive care unit following sudden cardiopulmonary arrest occurring at home. The electrocardiogram showed cardiac asystole, which was refractory to prolonged resuscitation efforts. Postmortem analyses detected RSV by polymerase chain reaction in an abundant, exudative pericardial effusion. Histopathological examination was consistent with viral myoepicarditis, including an inflammatory process affecting cardiac nerves and ganglia. Molecular analysis of sudden unexplained death genes identified a heterozygous mutation in myosin light chain 2, which was also found in two other healthy members of the family. Additional expert interpretation of the cardiac histology confirmed the absence of arrhythmogenic right ventricular dysplasia or hypertrophic cardiomyopathy.ConclusionsRSV-related sudden death in a normally developing child of this age is exceptional. This case highlights the risk of extrapulmonary manifestations associated with this infection, particularly arrhythmia induced by inflammatory phenomena affecting the cardiac autonomic nervous system. The role of the mutation in this context is uncertain, and it is therefore necessary to continue to assess how this pathogenic variant contributes to unexpected sudden death in childhood.
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页数:8
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