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Cardiac involvement in a female patient with Beçhet's disease: newer diagnostic and therapeutic approaches-a case report.
Eur Heart J Case Rep
November 2024
Department of Cardiology, University of Athens Medical School, Hippokration General Hospital, 114 Vasilissis Sofias Avenue, Athens 11527, Greece.
Background: Behçet's disease (BD) is a multisystemic chronic inflammatory disorder. Cardiac manifestations in BD are extremely rare. There have been no reports of cardiac involvement of BD and especially endomyocardial fibrosis in the left ventricle (LV).
View Article and Find Full Text PDFA fiery heart: case report of perimyocarditis in a patient with eosinophilic granulomatosis with polyangiitis.
Eur Heart J Case Rep
September 2024
Division of Cardiology, Cook County Health, 1969 W. Ogden Ave, Chicago, IL 60612, USA.
Background: Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare disease caused by small- to medium-sized vessel vasculitis which can also impact the heart. Because of its rarity and diverse clinical manifestations, diagnosis can be challenging. Here, we present a unique case of EGPA causing perimyocarditis in a young female patient.
View Article and Find Full Text PDFDistinguishing hypertensive cardiomyopathy from cardiac amyloidosis in hypertensive patients with heart failure: a CMR study with histological confirmation.
Int J Cardiovasc Imaging
December 2024
Division of Cardiovascular Medicine, The Ohio State University Wexner Medical Center, 452 W 10th Ave Columbus, Columbus, OH, 43210, USA.
Purpose: Differentiation of the cause of left ventricular hypertrophy (LVH) is challenging in cases with co-existing hypertension. CMR offers assessment of diffuse myocardial abnormalities via T1 mapping with extracellular volume fraction (ECV) and macroscopic fibrosis via late gadolinium enhancement imaging (LGE). The goal of the study was to understand if CMR parameters can differentiate hypertensive cardiomyopathy (HC) from cardiac amyloidosis (CA) in patients with hypertension and heart failure, using endomyocardial biopsy (EMB) as the gold standard.
View Article and Find Full Text PDFMyocardial infarction in a 17-year-old patient diagnosed with MPOD II syndrome.
Cardiol Young
October 2024
Medical and surgical unit of Congenital and Paediatric Cardiology, Reference Centre for Complex Congenital Heart Defects-M3C, University Hospital Necker-Enfants Malades, Paris, France.
Introduction: Microcephalic osteodysplastic primordial dwarfism (MOPD) syndrome type 2, caused by a mutation in the PCNT gene (21q22.3), is a rare autosomal recessive disorder. Patients present with bone dysplasia, insulin resistance, kidney diseases, and cardiac malformations, making them prone to vascular diseases.
View Article and Find Full Text PDFElectrocardiographic Findings in Diffuse Subendocardial Ischemia.
N Engl J Med
September 2024
Rambam Health Care Campus, Haifa, Israel
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