Successful atrial septal defect transcatheter closure in 
a patient with pentalogy of Cantrell and ectopia cordis

Gałeczka, Michał; Fiszer, Roland; Knop, Mateusz; Smerdziński, Sebastian; Szkutnik, Małgorzata; Białkowski, Jacek

doi:10.5114/aic.2019.86018

Cited by 5 publications

(4 citation statements)

References 11 publications

(12 reference statements)

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“…McMahon describes the case of a patient with double outlet right ventricle and pulmonary outflow tract obstruction with successful stent implantation in the ventricular outflow tract. 3 Galeczka describes percutaneous atrial septal defect closure procedure in a patient, 4 while Tanaka describes a pulmonary valvuloplasty performed by ventricular puncture in a patient with pentalogy of Cantrell and ectopia cordis. 5 Percutaneous stent implantation in the pulmonary outflow tract ensures better anterograde flow to the pulmonary arteries, improving the patient's saturation and promoting the growth of the pulmonary arteries.…”

Section: Discussionmentioning

confidence: 99%

Stent Implantation in the Right Ventricular Outflow Tract to Pulmonary Artery in a Child with Pentalogy of Cantrell: Case Report

Lombardi,

Calamita,

Tannus

et al. 2024

ABC Imagem Cardiovascular

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Section: Discussionmentioning

confidence: 99%

Stent Implantation in the Right Ventricular Outflow Tract to Pulmonary Artery in a Child with Pentalogy of Cantrell: Case Report

Lombardi,

Calamita,

Tannus

et al. 2024

ABC Imagem Cardiovascular

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“…We believe that staged operation is more appropriate, which is consistent with the literature report ( 7 ): if the congenital heart disease of PC patients is not so serious as to pose no threat to life, then the early surgical intervention is mainly to repair the abdominal wall muscles and diaphragm, so as to let the heart return to the chest at first, and if the heart structure is abnormal, we can judge whether or when to perform the operation according to the results of long-term follow-up. In recent years, there have been some reports of treatment of some such extraordinary heart defects in PC with transcatheter methods ( 10 , 11 ). However, this reported case was diagnosed with aortic arch hypoplastic and coarctation, and a large VSD.…”

Section: Discussionmentioning

confidence: 99%

Surgical treatment of neonatal Cantrell pentalogy: a case report and literature review

Liao¹,

Huang²,

Li³

2023

AME Case Rep

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Background Pentalogy of Cantrell (PC) is a congenital multiple malformation consisting of midline supraumbilical thoracoabdominal wall defects, anterior and pericardial diaphragm defects, lower sternum defects, ectopia cordis and various intracardiac anomalies, that present a distinctive challenge for care-providers and surgeons. Case Description Cases of PC in twin pregnancies is rare. We report a new born infant, weighing 2,400 g, the younger twin. After birth, he was transferred to the Children’s Hospital of Soochow University due to the prenatal echocardiography indicated that he has ventricular septal defect (VSD), atrial septal defect (ASD) and aortic arch hypoplasia. From the appearance, the lower end of sternum is suspiciously missing, the apical beating point is located at the lower edge of the median xiphoid process of sternum, and the upper abdominal muscle below the beating area is defective. He has the clinical and imaging features of complete type of PC. Three surgical operations were performed in the neonatal period, including end-to-side anastomosis of aortic arch under cardiopulmonary bypass (CPB), patch repair of VSD, repair of ASD, ligation of ductus arteriosus, correction of cardiac vascular malformation and repair of chest and abdominal wall defect, and the postoperative recoveries went smoothly. Conclusions PC is a rare congenital dysplasia, and its condition is complex. Our case shows that surgery is an effective treatment method, and the prognosis is related to the complexity of malformations.

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“…According to many researchers, the effectiveness and success of treatment as well as long-term survival depend primarily on the type of diagnosed heart defect. In recent years, some new aspects of Pentalogy of Cantrell management, such as the fetal diagnostic possibilities and the possible transcatheter interventions, could improve the survival of such patients [8][9][10]. However, first, these management were used for newborn or infant.…”

Section: Discussionmentioning

confidence: 99%

A Rare Long Term Survival Case of Complete Pentalogy of Cantrell in Adult after One-Staged Surgery

Hong¹,

Dong²,

Xie³

et al. 2021

Congenital Heart Disease

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Pentalogy of Cantrell is a rare congenital abnormality. Even with high-quality medical care and staged corrective surgeries in professional hospitals, the mortality rate is still very high and long-term prognosis is poor. Survival is largely determined by the complexity and severity of cardiac abnormalities, the efficiency of abdominal wall closure and postoperative complications. A 24-year-old male patient with complete pentalogy of Cantrell was diagnosed. One-stage surgical repair of all abnormalities were completed. The patient recovered well and had been follow-up for 7 years. He has a good cosmetic outcome, with no signs of cardiac dysfunction. No complications were noted.

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Successful atrial septal defect transcatheter closure in a patient with pentalogy of Cantrell and ectopia cordis

Cited by 5 publications

References 11 publications

Stent Implantation in the Right Ventricular Outflow Tract to Pulmonary Artery in a Child with Pentalogy of Cantrell: Case Report

Stent Implantation in the Right Ventricular Outflow Tract to Pulmonary Artery in a Child with Pentalogy of Cantrell: Case Report

Surgical treatment of neonatal Cantrell pentalogy: a case report and literature review

A Rare Long Term Survival Case of Complete Pentalogy of Cantrell in Adult after One-Staged Surgery

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