메뉴 건너뛰기

A · S · H

  • Summary Amyloidosis(아밀로이드증) file

    Introduction Amyloidosis is characterized by extracellular deposition of amyloid protein. Amyloid deposit can occurred in various organs including heart, kidney, liver, etc., and cardiac amyloidosis (CA) is refers to the amyloid deposit in heart tissue causing progressive thickening of cardiac walls and restrictive cardiomyopathy. Two main forms of amyloidosis affect heart, AL amyloidosis and amyloid transthyretin (ATTR)-related amyloidosis. Clinical manifestation Cardiac manifestations of CA in...

  • Summary 심장 유육종증 (cardiac sarcoidosis) file

    Introduction Sarcoidosis is an inflammatory disease involving any organs of the body characterized by non-caseating granuloma. Lung involvement is most common and followed by skin and lymph node. Cardiac sarcoidosis (CS) can be diagnosed as a part of systemic sarcoidosis or detected alone. Several studies described variable range of myocardial involvement in patients with systemic sarcoidosis; 2-5% in retrospective study of systemic sarcoidosis patients and 25-75% in autopsy studies. Disease spe...

  • Summary Hypertrophic cardiomyopathy(비대심근병증) file

    Introduction Hypertrophic cardiomyopathy (HCM) is defined by increased left ventricular wall thickness without evidence of abnormal loading condition, such as hypertension or aortic stenosis. HCM is the most common genetic cardiac disorder that affects one of 500 of general population. Majority of patients have benign course, meanwhile some patients experience heart failure, atrial fibrillation, stroke and sudden cardiac death (SCD). Clinical manifestation Most patients with HCM are asymptomatic...

©2013 KSODESIGN.All Rights Reserved