A 16-month-old girl was referred for tachycardia and upper respiratory tract infection. Echocardiographic examination revealed pericardial effusion, mild mitral regurgitation, and left ventricle systolic dysfunction. Patient was positive for Parainfluenza type 4 virus. Her laboratory tests revealed increased troponin I level. The patient was treated with intravenous immunoglobulin considering acute viral myopericarditis. Two weeks after treatment, midventricular hypertrophy was detected.
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http://dx.doi.org/10.1017/S1047951122003821 | DOI Listing |
Cardiol Young
July 2023
Pediatric Cardiology, Yildirim Beyazit University, Ankara, Turkey.
A 16-month-old girl was referred for tachycardia and upper respiratory tract infection. Echocardiographic examination revealed pericardial effusion, mild mitral regurgitation, and left ventricle systolic dysfunction. Patient was positive for Parainfluenza type 4 virus.
View Article and Find Full Text PDFBMJ Case Rep
March 2022
Department of Cardiology, Amrita Institute of Medical Sciences, Cochin, Kerala, India.
In this study, we discuss a female patient referred to cardiology with left ventricular hypertrophy at mid-ventricular segments resulting in a mid-cavitary obstruction and a left ventricular apical aneurysm. The patient had normal epicardial coronary arteries, but presented with recurrent cerebrovascular events. The patient had a positive family history for sudden cardiac death.
View Article and Find Full Text PDFAnn Noninvasive Electrocardiol
January 2021
Department of Medicine, University of Colorado School of Medicine, Aurora, CO, USA.
A primigravida 26-year-old woman who had developed pre-eclampsia with malignant hypertension at 30 weeks of gestation suffered acute myocardial infarction two days postpartum. Electrocardiogram demonstrated diffuse ST-segment depression suggestive of subendocardial ischemia. Echocardiography demonstrated focal asymmetric left ventricular hypertrophy, with a characteristic "basal septal bulge", and a left ventricular mid-cavitary gradient of 51 mmHg.
View Article and Find Full Text PDFWorld J Clin Cases
June 2015
Marie-France Poulin, Alap Shah, Richard G Trohman, Christopher Madias, Department of Medicine, Division of Cardiology, Rush University Medical Center, Chicago, IL 60612, United States.
A 54-year-old female with Anderson-Fabry disease (AFD)-R342Q missense mutation on exon 7 in alpha-galactosidase A (GLA) gene - presented with sustained ventricular tachycardia. Imaging confirmed the presence of a new left ventricular apical aneurysm (LVAA) and a significantly reduced intra-cavitary gradient compared to two years prior. AFDcv is an X-linked lysosomal storage disorder caused by GLA enzyme deficiency.
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