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The Journal of Thoracic and Cardiovascular Surgery, Vol 81, 887-896, Copyright © 1981 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
RH Anderson, SP Allwork, SY Ho, CC Lenox and JR Zuberbuhler
On the basis of previous experience, we have analyzed the anatomy of a
series of 53 hearts catalogued as having tetralogy of Fallot in the museum
of the Children's Hospital of Pittsburgh. All hearts had a ventricular
septal defect, aortic overriding, infundibular pulmonary obstruction, and
right ventricular hypertrophy. None of the hearts had been operated upon
during life. We paid particular attention to features of surgical
importance. Thus the ventricular septal defect was found to be of variable
form. It was perimembranous in 42 hearts. In 11 hearts it had entirely
muscular rims and in the remaining heart it was roofed by the conjoined
aortic and pulmonary valve rings (subarterial). From our previous
histologic experience, it was evident that this varying morphology
significantly affected the surgical anatomy of the atrioventricular
conduction tissues. We endeavored to display this disposition as might be
viewed by the surgeon. The degree of aortic override was variable, the
aortic valve being connected by 15% to 95% to the right ventricle. In 17
hearts more than half the aortic valve was attached to right ventricular
musculature. The nature of the infundibular obstruction also varied
markedly. In all cases (except the one with absent infundibular septum) the
infundibular septum was deviated in cephalad and anterior direction so as
to produce obstruction. In the majority of hearts further anatomic
structures also contributed to the obstruction. In some hearts there was
hypertrophy of the infundibular septum, particularly at its junction with
the trabecular septum. In others there was hypertrophy of the trabecula
septomarginalis, and in many hearts there was hypertrophy of additional
anterior infundibular trabeculations. The pulmonary valve was the narrowest
point of the outflow tract in only six hearts, but in many of the others,
it was abnormal. The results emphasize that while hearts may exhibit the
classical features of tetralogy of Fallot, there is usually considerable
individual variation in each of these features which is of major surgical
significance.
ARTICLES
Surgical anatomy of tetralogy of Fallot
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