Abstract

1. Abstract
1.1. Objective: to explore the pathophysiology, prenatal and postnatal diagnosis, treatment, surgical methods and prognosis of Cantrell pentalogy.
1.2. Methods: The clinical data of a neonate with Cantrell pentalogy were analyzed retrospectively, and the related literatures were reviewed.
1.3. Results: The clinical and imaging features of the children were consistent with the diagnosis of Cantrell's pentalogy. Three surgical operations were performed in the neonatal period, including end-to-side anastomosis of aortic arch under cardiopulmonary bypass, patch repair of ventricular septal defect, repair of atrial septal defect, ligation of arterial catheter, correction of cardiac vascular malformation and repair of chest and abdominal wall defect, and the postoperative recovery was in good condition.
1.4. Conclusion: Cantrell pentalogy is a rare congenital dysplasia, and its condition is complex. Surgery is an effective treatment method, and the prognosis is related to complicated malformation