scholarly journals Congenital Infundibular Stenosis

2020 ◽  
Author(s):  
Anaesthesia ◽  
1960 ◽  
Vol 15 (1) ◽  
pp. 45-47 ◽  
Author(s):  
H. A. CONDON ◽  
P. F. S. LEE

PEDIATRICS ◽  
1957 ◽  
Vol 19 (6) ◽  
pp. 1139-1147
Author(s):  
Mary Allen Engle

Dr. Engle: When pulmonic stenosis occurs as an isolated congenital malformation of the heart, it usually is due to fusion of the valve cusps into a dome with a small hole in the center. In Figure 1 the pulmonary artery has been laid open so that one can see the three leaflets of the pulmonary valve are completely fused, and that there is only a small, central, pinpoint opening which permits blood to leave the right ventricle and enter the pulmonary circulation. Valvular pulmonic stenosis is much more common than subvalvular or infundibular stenosis, where the obstruction to pulmonary blood flow lies within the substance of the right ventricle. There it may be due to a diaphragm of tissue which obstructs the outflow of the right ventricle, or to an elongated narrow tunnel lined with thickened endocardium, or to a ridge of fibrous or muscular tissue just beneath the pulmonary valve. The changes in the cardiovascular system which result from obstructed pulmonary blood flow are so characteristic that they permit the ready recognition of this condition. Proximal to the constriction, these changes manifest the burden placed on the right ventricle, which enlarges and hypertrophies. On physical examination this is demonstrated by the precordial bulge and tapping impulse just to the left of the sternum, where the rib cage overlies the anterior (right) ventricle. Radiographically, both by fluoroscopy and in roentgenograms in the frontal and both oblique views, right ventricular enlargement is seen. In the electrocardiogram, the precordial leads show a pattern of right ventricular hypertrophy.


2016 ◽  
pp. 339-345
Author(s):  
Petrişor A. Geavlete ◽  
Gheorghe Niţă ◽  
Răzvan Mulţescu ◽  
Cristian Moldoveanu ◽  
Bogdan Geavlete

Urology ◽  
2002 ◽  
Vol 60 (2) ◽  
pp. 344 ◽  
Author(s):  
Michael J Nurzia ◽  
Alexandru R Costantinescu ◽  
Joseph G Barone

2004 ◽  
Vol 23 (4) ◽  
pp. 285-292 ◽  
Author(s):  
Randall Craver ◽  
Rebecca Boyd ◽  
Kenneth Ward ◽  
Edwin Harmon

2014 ◽  
Vol 13 (1) ◽  
pp. eV45
Author(s):  
V. Mirciulescu ◽  
R. Multescu ◽  
D. Georgescu ◽  
G. Nita ◽  
C. Moldoveanu ◽  
...  

1998 ◽  
Vol 8 (4) ◽  
pp. 440-442
Author(s):  
Antoinette M. Cilliers ◽  
Kathy M. Vanderdonck ◽  
Jan P. du Plessis ◽  
Stefanus L. Cronje ◽  
Solomon E. Levin

AbstractThe finding of bland, sterile vegetations in children with severe tetralogy of Fallot is unexpected, and to our knowledge, has not been reported previously. Eight patients diagnosed with tetralogy between January 1993 and July 1997 had sterile vegetations proven by histological and microbiological evaluation, in their right ventricular outflow tracts. Four of these patients were experiencing severe hyper-cyanotic spells, and four had severely reduced effort tolerance at presentation. They all underwent cardiac catheterization and were submitted for surgical repair. At surgery, the vegetations were thought to be causing further narrowing of the already tight fibrotic infundibular stenosis. Two of these patients had evidence of damaged valves, without evidence of active endocarditis. Although initially sterile, these vegetations, may in some instances, become infected.


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