نتایج جستجو برای: tetralogy of fallot coronary vessel anomalies echocardiography

تعداد نتایج: 21211118  

Journal: :the journal of tehran university heart center 0
saeed davoodi national iranian oil company central hospital, tehran, iran. yaddollah dadashi national iranian oil company central hospital, tehran, iran. manouchehr madani civi national iranian oil company central hospital, tehran, iran. seyed hesameddin abbasi national iranian oil company central hospital, tehran, iran. amir hossien sami national iranian oil company central hospital, tehran, iran. kyomars majdi national iranian oil company central hospital, tehran, iran.

in this paper, we describe a case of an aneurysmal circumflex artery connected to the coronary sinus through a fistula in a 40-year-old man with a two-year history of palpitation and chest pain. we discussed surgical management for patients with coronary artery fistula (caf), particularly for asymptomatic patients with a small left-to-right shunt .

2009
Jung Yun Choi

= Abstract = Sewn years' experience of fetal echocardiography was reviewed to assess the diagnostic accuracy of fetal echocardiography, distribution of individual cardiac anomalies, and some practical problems of fetal echocardiography in Korea. A total of 737 fetuses IMlre examined and 45 confirmed and 20 unconfirmed cardiac structural anomalies IMlre identified. In general, fetal echocardiogr...

Journal: :acta medica iranica 0
khosrow hashemzadeh department of cardiovascular surgery, cardiovascular research center, shahid madani hospital, tabriz university of medical sciences, tabriz, iran. shahryar hashemzadeh department of general and thoracic surgery, imam reza hospital, tabriz university of medical sciences, tabriz, iran.

the purpose of this study was to evaluate the early and late outcome after total correction of tetralogy of fallot (tof) in 101 consecutive patients with a mean age of 8.23 ± 4.90 years underwent repair of surgery at one institution between 1995 and 2006. forty two patients had initial palliative operations. a transannular patch was inserted in 60 (58.5%) patients. risk factors for operative mo...

Journal: :the journal of tehran university heart center 0
mohammadreza pourbehi the persian gulf nuclear medicine research centre, bushehr university of medical sciences, bushehr, iran. abdolatif amini department of cardiology, medical faculty, bushehr university of medical sciences, bushehr, iran. shokrollah farrokhi the persian gulf tropical medicine research center, bushehr university of medical sciences, bushehr, iran.

congenital anomalies of coronary arteries, albeit rare, may be significant contributors to angina pectoris, hemodynamic abnormalities, and sudden cardiac death. a 47-year-old man referred to us with atypical chest pain. electrocardiography demonstrated no significant ischemic changes, but cardiac troponin i test was positive. the patient underwent coronary angiography, which revealed a single c...

Journal: :the journal of tehran university heart center 0
arash gholoobi atherosclerosis prevention research center, imam reza hospital, mashhad university of medical sciences, mashhad, iran. mohammad vojdanparast cardiovascular research center, mashhad university of medical sciences, mashhad, iran.

large intercoronary communications in the absence of obstructive coronary artery disease constitute a very rare coronary artery anomaly in which there is a readily visible connection between the 2 coronary arteries with a unidirectional or bidirectional blood flow; consequently, this anomaly may be misinterpreted as a functioning collateral vessel, indicative of an unrecognized proximal coronar...

Journal: :Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese 2005
George E Sarris

T etralogy of Fallot is the most common cyanotic congenital heart lesion. Its anatomical features were first described by Stenson in 1672. In 1888 Fallot published his clinical observations, linking the four elements he considered to be the main anatomical abnormalities (interventricular septal defect, stenosis of the right ventricular outflow tract, right ventricular hypertrophy and an aorta t...

Journal: :Texas Heart Institute journal 2013
Elisa Bradley Jeff Parker Eric Novak Philip Ludbrook Joseph Billadello Ari Cedars

Patients with tetralogy of Fallot can survive to late adulthood; however, there are few data on cardiovascular outcomes in this population. We conducted a single-center retrospective analysis of cardiovascular outcomes and risk factors in 208 patients with tetralogy of Fallot to better evaluate the burden of cardiovascular disease in this group. Descriptive statistics were used to determine the...

Journal: :iranian journal of medical sciences 0
alwaleed al-dairy department of cardiovascular surgery, rajaie cardiovascular medical and research center, iran university of medical sciences, tehran, iran yousef rezaei heart valve disease research center, rajaie cardiovascular medical and research center, iran university of medical sciences, tehran, iran maziar gholampour dehaki department of cardiovascular surgery, rajaie cardiovascular medical and research center, iran university of medical sciences, tehran, iran anita sadeghpour echocardiography research center, rajaie cardiovascular medical and research center, iran university of medical sciences, tehran, iran zia totonchi department of cardiac anesthesia, rajaie cardiovascular medical and research center, iran university of medical sciences, tehran, iran hamidreza pouraliakbar department of radiology, rajaie cardiovascular medical and research center, iran university of medical sciences, tehran, iran

anomalous origin of the left coronary artery from the pulmonary artery (alcapa) is a rare congenital cardiac malformation. we report three cases of alcapa who survived to adulthood. the first case was a 51-year-old woman who complained of typical chest pain that was diagnosed with alcapa using cardiac catheterization and coronary computed tomographic angiography (cta). the second case was a 30-...

2009
Tayfun Sahin Teoman Kilic Umut Celikyurt Ulas Bildirici Dilek Ural

Persistent left superior vena cava is a rare congenital venous anomaly. It results from failure of closure of the left anterior cardinal vein during cardiac development. It is usually asymptomatic but can be associated with other congenital cardiac defects including atrial septal defects, ventricular septal defects, endocardial cushion defects, tetralogy of Fallot and rhythm disturbances. PLSVC...

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