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. 2020 Jul 16;8:347. doi: 10.3389/fped.2020.00347

Table 1.

Anamnestic, histological, and microbiologic preoperative data.

Patient# Gender Age (m) Weight
(kg, percentile)
Type of DCM Histology Aspecific symptoms prior admission Viral test
1 M 8.6 8.0,
10th percentile
LV non-compaction cardiomyopathy
[heterozygous mutation of TPM1 gene° (de novo) and of ABCC9 gene (parental)]
Not performed Yes Not performed
2 M 42.2 12.0,
3rd percentile
Fulminant myocarditis in idiopathic unrecognized DCM Active lymphocytic myocarditis with endocardial fibroelastosis Yes Negative
3 M 3.9 5.9, 10th−25th percentile Acute myocarditis Active lymphocytic myocarditis with endocardial fibroelastosis No CMV-DNA positive on blood and urine samples, negative in myocardial biopsy
4 F 12.5 7.7,
<3rd percentile
PVB19 chronic myocarditis Chronic myocarditis in activity Phase Yes PVB19 on blood sample and myocardial biopsy
5 M 5.7 4.8,
<3rd percentile
Acute myocarditis Active lymphocytic myocarditis No HHV6-DNA positive on blood sample, genomic integration in patient's cells, negative in myocardial biopsy

CMV, cytomegalovirus; DCM, dilated cardiomyopathy; PVB19, parvovirus B19; LV, left ventricular.

°associated with non-compaction cardiomyopathy.