Literature DB >> 19717356

Uncorrected pink tetralogy of Fallot in an adult patient: incidental CT findings.

Thanongchai Siriapisith1, Jitladda Wasinrat, Damras Tresukosol.   

Abstract

Tetralogy of Fallot (TOF), one of the most common congenital heart diseases, has four major components: right ventricular hypertrophy, overriding aorta, membranous ventricular septal defect, and right ventricular outflow tract obstruction. If not already present at birth, cyanosis develops in the first year of life. Survival of the patient depends on the degree of pulmonary obstruction and the pulmonary blood supply. Patients rarely survive after the fourth decade of life. Limitation of blood to the lungs combined with ventricular septal defect results in supply of oxygen-poor blood to the body, causing cyanosis (blue coloration) in the patient. If the pulmonary stenosis is mild and ventricular septal defect is in balance, however, the noncyanotic patient is referred as having "pink tetralogy of Fallot." 2010 Society of Cardiovascular Computed Tomography. Published by Elsevier Inc. All rights reserved.

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Year:  2009        PMID: 19717356     DOI: 10.1016/j.jcct.2009.08.002

Source DB:  PubMed          Journal:  J Cardiovasc Comput Tomogr        ISSN: 1876-861X


  1 in total

1.  Right ventricular outflow tract obstruction caused by double-chambered right ventricle presenting in adulthood.

Authors:  John Kokotsakis; Efthymia G Rouska; Leanne Harling; Hutan Ashrafian; Vania Anagnostakou; Christos Charitos; Thanos Athanasiou
Journal:  Tex Heart Inst J       Date:  2014-08-01
  1 in total

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