Exaggerated responses to hypertension or prolonged physical training may produce left ventricular hypertrophy closely mimicking hypertrophic cardiomyopathy but disarray is absent. Such cases may die suddenly. H
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disease with an incidence of 1:5001. Hallmarks of HCM are cardiomyocyte disarray, interstitial fibrosis, and hypertrophy of the left ventricle2,3. Disease progression can be variable among affected families and individuals with sympt...
Primary or idiopathic cardiomyopathies describe a clinical syndrome cused by generalized heart muscle diseases of unknown cause and are devided into dilated, hypertrophic and restrictive types. All types of cardiomyopathy are an important cause of morbidity and mortality in animals. In contrast to sec...
—— 水性肿胀(水样变性)hyperplasia —— 增生hypertension —— 高血压hypertrophic cardiomyopathy —— ...
hypertrophic cardiomyopathy <病理学Pathology)> 肥厚型心肌病 hypertrophy <病理学Pathology)> 肥厚 infarct <病理学Pathology)> 梗死 infectious hepatitis <病理学Pathology)> 传染性肝炎 infiltration <病理学Pathology)> 浸润 inflammation <病理学Pathology)> 炎症 ...
Answer: C (Thick interventricular septum) and E (β-myosin heavy chain gene) Explanation: The pathologic change illustrated in the image is myofiber disarray, which is characteristic of hypertrophic cardiomyopathy, which is associated with sudden cardiac death. Gross features of this disease process ...
Macrosomia along with the cardiac, pancreatic and hepatic findings suggested the diagnosis of cardiomyopathy secondary to maternal diabetes. Conclusions: Hypertrophic cardiomyopathy is a common finding in infants of diabetic mothers and most often resolves without intervention within the first 6 months of ...
Hughes SE (2004) The pathology of hypertrophic cardiomyopathy. Histopathology 44(5):412–427 Article CAS PubMed Google Scholar Tansey DK, Aly Z, Sheppard MN (2005) Fat in the right ventricle of the normal heart. Histopathology 46(1):98–104 Article CAS PubMed Google Scholar Skopp G (...
Rodríguez JE, McCudden CR, Willis MS.Familial hypertrophic cardiomyopathy: basic concepts and future molecular diagnostics.Clin Biochem2009;42:755–765. ArticlePubMedGoogle Scholar Shoen FG.Surgical pathology of removed natural and prosthetic heart valves.Hum Pathol1987;18:558–567. ...
Hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, and restrictive cardiomyopathy are the most prevalent forms of cardiomyopathy. 8.3.12 Congenital heart disease The malformation of the heart that is apparent at birth is referred to as congenital heart disease...