Tetralogy of Fallot
نویسندگان
چکیده
Hearts with Fallot's tetrad from 33 children dying at the age from 14 days to 8 years were studied. Analysis of the morphological features of the defect revealed its typical anatomic signs: anteroleft shift of conic septum (oblique orientation); reorientation of the structures of inflow and outflow parts of the right ventricle infundibular pulmonary stenosis the occurrence of which may be due to all the structures and formations participating in the formation of the outflow part of the right ventricle. Four main types of stenoses were established. The most frequent cause of maximal stenosis of the blood flow through the right ventricle was demarcating muscle ring; a nonrestrictive defect of the ventricular septum (DVS). Three types of DVS in Fallot's tetrad were found: perimembranous, muscular, subarterial; dextroposition of the aorta, and right ventricular hypertrophy.
منابع مشابه
بررسی عملکرد بطنها با اکوکاردیوگرافی در نارسایی دریچه ریوی پس از جراحی تترالوژی فالوت
Background: Tetralogy of Fallot is the most common cyanotic congenital heart disease. The systolic and diastolic function in both ventricles is altered even after successful corrective surgery for this defect with a transannular patch. Pulmonary regurgitation, a common complication after this treatment, is usually well tolerated in childhood. The aim of this study was to assess the combined dia...
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Background Total correction of Tetralogy of Fallot (TOF) anomaly in early childhood has been practiced in many centers with good results, but in some of patients after few years sever Pulmonary valve insufficiency occurred. Materials and Methods At a cross- sectional study from January 2015 to January 2016, 10 patients who had history of primary repair of TOF with free pulmonary insufficiency (...
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Congenital aortocaval fistula in association with complex congenital heart disease has never been described before. We represent an adult with tetralogy of fallot and an undiagnosed subclavian artery to superior vena cava fistula in previous catheterisms. He underwent surgical correction, successfully. After 8 months post operation he was doing well with improved functional capacity and no ...
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ورودعنوان ژورنال:
- Orphanet Journal of Rare Diseases
دوره 4 شماره
صفحات -
تاریخ انتشار 1958