An unrepaired persistent truncus arteriosus in a 62-year-old adult

2016 ◽  
Vol 17 ◽  
pp. e124-e125 ◽  
Author(s):  
Giordano Zampi ◽  
Andrea Celestini ◽  
Fabrizio Benvissuto ◽  
Pietro Scrimieri ◽  
Amedeo Pergolini ◽  
...  
2021 ◽  
Author(s):  
SENAI Goitom SEREKE ◽  
Hamdi Mohamed Isse ◽  
Tamale Jaffar ◽  
Felix Bongomin

Abstract Background: Persistent truncus arteriosus (TA) is a rare congenital heart condition with reported incidence of 1.2% among all congenital heart malformations. Majority of patients with TA die early in childhood due to complications such as heart failure. Case presentation: An 18-year-old adult with unsuspected congenital heart disease since birth, not detected in childhood. Six months prior to his presentation, he complained of easy fatigability and paroxysmal nocturnal dyspnea. Chest radiography demonstrated normal heart size and electrocardiogram showed biventricular hypertrophy. Echocardiograph showed truncus arteriosus type II with large outlet ventricular septal defect. The patient was put on medical therapy including bed rest, fluid restriction and then surgical correction was done. The patient’s symptom improved after the surgical correction.Conclusion: TA is a rare, serious congenital heart defect that can be detected in prenatal period by routine ultrasound screening. It is also very rare for TA to be silent and reach adulthood without clinical manifestation and a diagnosis.


2021 ◽  
Vol 4 (5) ◽  
pp. 01-04
Author(s):  
Miguel Maluf

We report long-term outcome after one-stage, surgical repair, in a two months-old girl with persistent truncus arteriosus type I, II. The operation was carried out with the remodeling of the right ventricle, using a swine bicuspid pulmonary prosthesis. Twenty-six years later, the patient is in excellent clinical condition, CF I (NYHA), with normal peripheral oxygen saturation. Recent invasive and not invasive imaging show: absence of intracardiac shunt and growing of the right ventricle outlet tract and discrete double lesion of the pulmonary valve. The pulmonary flow directed uniformly for both lungs. In selected cases, the long-term prognosis of patients with persistent truncus arteriosus, undergoing early surgical repair, avoiding the use of valved conduit, makes for an excellent evolution, without new interventions. Endovascular procedures, now well standardized, for the implantation of a pulmonary valve stent, through a catheter, will allow an effective approach, in the presence of late obstructions, in patients who have undergone right ventricular remodeling, without the use of valved conduits.


Ultrasound ◽  
2017 ◽  
Vol 25 (4) ◽  
pp. 251-254
Author(s):  
Maryam Nabati

Persistent truncus arteriosus is a rare congenital cardiac malformation. It is characterized by a single great artery arising from the heart which supplies the aorta, the origin of coronary arteries and pulmonary arteries. Without surgery, prognosis is poor and 90% of these patients die before one year of age. We report a rare case of an asymptomatic 35-year-old woman with uncorrected persistent truncus arteriosus and hypoplastic right and left pulmonary arteries. Hypoplastic branch pulmonary arteries prevented the development of severe pulmonary arterial hypertension.


Heart ◽  
1968 ◽  
Vol 30 (6) ◽  
pp. 812-816 ◽  
Author(s):  
B E Victorica ◽  
I H Gessner ◽  
G L Schiebler

2020 ◽  
Vol 15 (1) ◽  
Author(s):  
Rawan M. Alamri ◽  
Ahmed M. Dohain ◽  
Amr A. Arafat ◽  
Ahmed F. Elmahrouk ◽  
Abdullah H. Ghunaim ◽  
...  

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