Background: Pediatric inflammatory multisystem syndrome temporally associated with SARS‐CoV‐2 (PIMS‐TS) is an inflammatory disease occurring in a small minority of children a few weeks after acute infection. Cardiac manifestations are common, but little is known about the potentially persistent heart changes after PIMS‐TS.Purpose: To analyze the frequency and type of myocardial complications of PIMS‐TS with initial cardiac involvement assessed with cardiac magnetic resonance imaging (MRI), including parametric imaging, performed 3 months after hospitalization.Study Type: Retrospective.Population: Nineteen consecutive children (median age 10 years, interquartile range (IQR) 10–15 years, 74% male).Field Strength/Sequence: Balanced steady state free precession (bSSFP, cine imaging), modified Look‐Locker (T1 mapping), T2‐prepared bSSFP (T2‐mapping), dark‐blood T2‐weighted turbo spin echo with fat suppression and phase sensitive inversion recovery (late gadolinium enhancement (LGE)) sequences at 1.5 T.Assessment: Patients were scanned after a median of 99 days (IQR 89–104 days) from the diagnosis. MR data were reviewed by three independent observers, with 13, 2, and 5 years' experience in cardiac MRI. Pre‐ and post‐contrast T1, T2, extra‐cellular volume, and T2 signal intensity (T2 SI) ratio were calculated. Diagnosis of acute myocarditis was based on modified Lake Louise criteria. Cardiac MRI parameters were compared, where possible, to previously published pediatric normal values.Statistical Tests: Interclass correlation coefficient and Bland–Altman repeatability analysis. A P‐value <0.05 was considered statistically significant.Results: Despite cardiac involvement including decreased left ventricular ejection fraction (LVEF) (median LVEF = 47%, IQR 43%–53%) and increased troponin I (median 101 ng/mL, IQR 50–661 ng/mL) during hospitalization, there were no persistent cardiac changes observed in cardiac MR at follow‐up. All patients had normal size and function of the left ventricle and normal precontrast T1 and T2 relaxation times. There were no signs of LGE. Persistent, mild pericardial effusion (8–9 mm) was found in three (16%) patients.Data Conclusion: There were no persistent changes on cardiac MRI in a group of children approximately 3 months post hospitalization due to PIMS‐TS with cardiac involvement. This supports the hypothesis that cardiac involvement during PIMS‐TS is a form of transient inflammatory response rather than direct and potentially persistent injury from the virus.Level of Evidence: 4Technical Efficacy: Stage 3

Physical training is associated with changes in cardiac morphology called the “athlete’s heart”, which has not been sufficiently studied in children. The aim of the study was to analyze cardiac adaptation to exercise in pre-adolescent soccer players. Thirty-six soccer players (mean age 10.1 ± 1.4 years) and 24 non-athlete male controls (10.4 ± 1.7 years) underwent cardiac magnetic resonance. Measurements of myocardial mass, end-diastolic and end-systolic volume, stroke volume and ejection fraction for left and right ventricle (LV, RV) were performed. Additionally, left and right atrial (LA, RA) areas and volumes were analysed. Relative wall thickness (RWT) was calculated to describe the pattern of cardiac remodeling. Interventricular wall thickness and LV mass were significantly higher in athletes, but remained within the reference (6.9 ± 0.8 vs. 6.2 ± 0.9 mm/√m², p = 0.003 and 57.1 ± 7.4 vs. 50.0 ± 7.1 g/m², p = 0.0006, respectively) with no changes in LV size and function between groups. The RWT tended to be higher among athletes (p = 0.09) indicating LV concentric remodeling geometry. Soccer players had significantly larger RV size (p < 0.04) with similar function and mass. Also, the LA volume (p = 0.01), LA area (p = 0.03) and LA diameter (p = 0.009) were significantly greater in players than in controls. Cardiac adaptations in pre-adolescent soccer players are characterized by an increased LV mass without any changes in LV size and systolic function, which is typical of resistance training with tendency to concentric remodeling. This is accompanied by increase of LA and RV size. It should be taken into account during annual pre-participation evaluation.

A better understanding of the left ventricle (LV) and right ventricle (RV) functioning would help with the differentiation between athlete’s heart and dilated cardiomyopathy (DCM). We aimed to analyse deformation parameters in endurance athletes relative to patients with DCM using cardiac magnetic resonance feature tracking (CMR-FT). The study included males of a similar age: 22 ultramarathon runners, 22 patients with DCM and 21 sedentary healthy controls (41 ± 9 years). The analysed parameters were peak LV global longitudinal, circumferential and radial strains (GLS, GCS and GRS, respectively); peak LV torsion; peak RV GLS. The peak LV GLS was similar in controls and athletes, but lower in DCM (p < 0.0001). Peak LV GCS and GRS decreased from controls to DCM (both p < 0.0001). The best value for differentiation between DCM and other groups was found for the LV ejection fraction (area under the curve (AUC) = 0.990, p = 0.0001, with 90.9% sensitivity and 100% specificity for ≤53%) and the peak LV GRS diastolic rate (AUC = 0.987, p = 0.0001, with 100% sensitivity and 88.4% specificity for >−1.27 s⁻¹). The peak LV GRS diastolic rate was the only independent predictor of DCM (p = 0.003). Distinctive deformation patterns that were typical for each of the analysed groups existed and can help to differentiate between athlete’s heart, a nonathletic heart and a dilated cardiomyopathy.

Background: Hepatic portal venous gas (HPVG) is a rare imaging finding in children. It can be an important manifestation of severe diseases such as necrotizing enterocolitis (NEC) in neonates or bowel wall rupture in older children. However, there are many other diseases presenting with HPVG that do not necessarily require a surgical intervention. Case Report: In the period between 2011–2015, there were 12 cases of HPVG in children aged up to 24 months in our hospital. We did not include children with NEC. We retrospectively analyzed clinical data and US examinations as regards the suspected causes and final diagnoses. Only 1 patient with HPVG required an immediate surgical intervention. This was – a 4-month-old girl 32 days after a repair of a congenital diaphragmatic hernia, with ultrasound signs of acute bowel wall necrosis. During surgery a bowel strangulation was revealed. Other causes included: – 4 patients with bowel inflammation (including complications of neoplastic diseases such as leukemia and Hodgkins’disease); – 3 patients with food allergy; – 1 patient with acute gastroenteritis; – 1 patient with hepatic injury because of a suspected metabolic disease; – 1 incidental finding revealed before closing a ventricular septum defect; – 1 patient during followup performed 2 weeks after a reconstruction of bowel continuity. Conclusions: HPVG is not always a sign of a life-threatening condition and it should not be by itself an indication for surgical treatment. HPVG requires a close monitoring of the clinical status, which is crucial for further management. In patients in non-severe clinical condition, we propose to perform a follow-up ultrasound imaging within 1–2 days, and not to extend diagnostic procedures, especially in case of ultrasound picture normalization. An abdominal ultrasound examination appears to be the method of choice for the identification of gas in the hepatic portal system in children.