An article reviews etiopathogenesis of cardiomyopathy. Regardless of the fact that many early days' fundamental investigations are devoted to cardiomyopathy problem, still there is no common consideration concerning the etiology, pathogenesis, morphogenesis, classification and therapy of cardiomyopathy as well. Problem concerning the etiology of cardiomyopathy appear of particular interest. Great number of authors put an emphasis on the role of coxsackie B viruses' group encompasses enteroviruses with well defined cardiotropic features. Smoking is believed to play significant role in the evolution of cardiomyopathy, having drastic effect on the oxidative and energetic processes of the cells. Consequently, the phrase "cardiomyopathy during smoking" seems quite relevant. On behalf of World Public Health Services recommendation the term cardiomyopathy encloses patients with myocarditis of unknown origin with well defined characteristic features - megalocardia and cardiac decompensation. However, heart valve, coronary and lung vessels injuries are excluded. Note worthily, concept "secondary cardiomyopathy" is not well interpreted, especially as in this case etiology is well understood. Due to the complexity of differential diagnostics for congestive cardiomyopathy and myocardial ischemia in present day literature the term "ischemic cardiomyopathy" is widely applicable. Frequently, patients with congestive cardiomyopathy and myocardial ischemia reveal identical clinical-angiocardiographic set of symptoms determined by generalized injury of cardiac muscle. Taking into account all the above mentioned data it is evident that regarding etio pathogenesis and morphogenesis cardiomyopathy is not completely explored pathology and needs further investigation. The goal here is revelation of factors affecting cardiac contractile function. Besides, elaboration of new, effective pharmaceutical means seems of great importance.
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Circ Heart Fail
January 2025
Assistance Publique Hopitaux de Paris (APHP), Pitié-Salpêtrière Hospital, Institute of Cardiology and Institute for Cardiometabolism and Nutrition, Paris, France (A.H., M.L., P. Charron, E.G.).
Transl Pediatr
December 2024
Department of Medicine, Dow Medical College, Karachi, Pakistan.
Transl Pediatr
December 2024
Department of Pediatric Intensive Care Unit, National Regional Medical Center, Guizhou Branch of Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Guizhou Provincial People's Hospital, Guiyang, China.
Background: Metabolic cardiomyopathy is characterized by structural and functional changes to the heart and interstitial fibrosis without coronary artery disease or hypertension. Inborn metabolic defects are a common cause of cardiomyopathy in children. There are more than 40 kinds of inborn metabolic defects that cause cardiomyopathy.
View Article and Find Full Text PDFJACC Case Rep
January 2025
Division of Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Structural abnormalities within the right ventricular outflow tract (RVOT) can present similarly to Brugada syndrome. A 34-year-old woman with no medical history presented with polymorphic ventricular tachycardia/ventricular fibrillation cardiac arrest and initial electrocardiogram showed type I Brugada pattern. Cardiac magnetic resonance imaging revealed prominent tissue thickening at the RVOT with late gadolinium enhancement.
View Article and Find Full Text PDFJACC Case Rep
January 2025
Division of Cardiothoracic Surgery, Department of Surgery, Virginia Commonwealth University, Richmond, Virginia, USA.
Extracavitary cardiac calcific amorphous tumors/masses are extremely rare. We present a case report of a 62-year-old man with end-stage renal disease who presented with extracavitary cardiac calcific amorphous tumors/masses compressing the biventricular outflow tracts, resulting in hemodynamic compromise and progressive limitation of activities. The patient was successfully treated with surgery, with complete resolution of symptoms and markedly improved quality of life.
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