Articles

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798 results found
Article

Thoracic aorta

The thoracic aorta is the most superior division of the aorta and is divided into three sections: ascending aorta aortic arch descending aorta The thoracic aorta begins at the aortic valve, located obliquely just to the left of the midline at the level of the third intercostal space. It term...
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Aortic root abscess

An aortic root abscess is a serious complication of infective endocarditis and most commonly seen in patients who have had aortic root repair and/or aortic valve replacement. Epidemiology Aortic root abscess occurs as a complication of infective endocarditis in 10-37% 9. Abscess formation in p...
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Aortic root

The aortic root is the first part of the aorta containing parts of the aortic valve and connects the heart to systemic circulation.  Gross anatomy The aortic root is located between the aortic annulus (the junction of the outflow tract of the left ventricle and the aortic valve) and the sinotu...
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Obliteration of the retrosternal airspace

Obliteration of the retrosternal airspace is a sign on lateral chest radiographs which can be due to anterior mediastinal mass or right ventricular hypertrophy.
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Pericardial lipoma

Pericardial lipomas are slowly growing benign tumors of the pericardium that are asymptomatic unless large in size, where they can cause pressure symptoms. Clinical presentation Pericardial lipomas are usually asymptomatic. Occasionally non-specific symptoms are present including: chest pain...
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Intracardiac thrombus

Intracardiac thrombi are seen in a variety of clinical settings and can result in severe morbidity or even death from embolic events. They can occur following myocardial infarction with ventricular thrombus formation, or with atrial fibrillation and mitral stenosis where atrial thrombi predomina...
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Watchman device

Watchman device is a permanent left atrial appendage closure device, which is percutaneously implanted to prevent embolization of thrombus from the appendage into the systemic circulation in cases of atrial fibrillation. It is used when there is a contraindication to anticoagulation or high risk...
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Left atrial appendage closure devices

Left atrial appendage (LAA) closure devices are implantable cardiac devices which are placed in the left atrial appendage for stroke prevention in patients with atrial fibrillation who have contraindications to pharmacological anticoagulation. Depending on the device they may be inserted percuta...
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Page kidney

Page kidney, or Page phenomenon, refers to systemic hypertension secondary to extrinsic compression of the kidney by a subcapsular collection, e.g. hematoma, seroma, or urinoma. Clinical presentation Patients present with hypertension, which may be recognized acutely after an inciting event or...
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Light chain amyloidosis

Amyloid light chain (AL) amyloidosis or immunoglobulin light chain amyloidosis is a systemic amyloidosis and a plasma cell proliferative disorder characterized by deposition of misfolded monoclonal kappa or lambda light chains produced by clonal plasma cells 1-6. Epidemiology Amyloid light cha...
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Cardiac dyssynchrony

Cardiac dyssynchrony refers to deviations in timing and/or disturbance of the normal sequence of activation and contraction between the atria and ventricles of the heart, the right and left ventricle or among the ventricular wall segments. Epidemiology Mechanical dyssynchrony is common in pat...
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Cardiogenic pulmonary edema

Cardiogenic pulmonary edema is a subtype of pulmonary edema where the underlying etiology is due to left ventricular dysfunction. Pathology Etiology left heart failure congestive cardiac failure mitral regurgitation aortic stenosis arrhythmias myocardial pathology myocarditis cardiomyo...
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Hypoplastic left heart syndrome

Hypoplastic left heart syndrome (HLHS) is a cyanotic congenital cardiac anomaly where affected individuals can have profound cyanosis and cardiac failure. It is one of the most common causes for a neonate to present with congestive cardiac failure and the 4th most frequent cardiac anomaly to ma...
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Major aortopulmonary collateral arteries

Major aortopulmonary collateral arteries (MAPCAs) are persistent tortuous fetal arteries that arise from the descending aorta and supply blood to pulmonary arteries in the lungs usually at the posterior aspect of the hilum. Pathology Embryologically, the intersegmental arteries regress with th...
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Caseous calcification of the mitral annulus

Caseous calcification, liquefactive necrosis or ‘toothpaste tumor’ of the mitral annulus refers to a calcified cardiac mass and a rare variant of mitral annular calcification that is often misdiagnosed as a cardiac abscess or cardiac tumor. Epidemiology Caseous mitral annular calcification is ...
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Apical hypertrophic cardiomyopathy

Apical hypertrophic cardiomyopathy (AHCM or ApHCM), also known as Yamaguchi syndrome, is a rare form of hypertrophic cardiomyopathy which usually involves the apex of the left ventricle, rarely involves the right ventricular apex, or involves both apices. Epidemiology Historically, this condit...
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Arrhythmogenic right ventricular cardiomyopathy diagnostic criteria

For the diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC) to be made, patients must have either two major criteria, one major and two minor criteria, or four minor criteria. Major criteria global or regional dysfunction and structural alterations: severe dilatation of the ri...
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Coronary artery bypass graft

A coronary artery bypass graft (CABG or CAG) is placed during a surgical procedure to increase blood flow to the myocardium due to coronary stenoses, usually caused by coronary artery disease. Arteries or veins can be grafted during this procedure. Long term outcome of coronary artery bypass gr...
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Aortopulmonary septal defect

Aortopulmonary septal defect (APSD) is a congenital anomaly where there is an abnormal communication between the proximal aorta and the pulmonary trunk in the presence of separate aortic and pulmonary valves. Terminology APSD should not be confused with the radiographic term aortopulmonary win...
Article

RASopathy

RASopathies are a class of developmental disorders caused by germline mutations in genes that encode for components or regulators of the Ras/mitogen-activated protein kinase (MAPK) pathway. Epidemiology As a group, RASopathies represent one of the most common malformation syndromes, with an in...

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