PRENATAL DIAGNOSIS OF CONGENITAL DIAPHRAGMATIC HERNIA BY ULTRASONOGRAPHY: A CASE REPORT
Abstract
A case of congenital diaphragmatic hernia diagnosed sonographically in utero at 20 weeks gestation is described. In previous reports, this diagnosis has been made as early as 15 weeks gestation'. Recognition of this severe abnormality in the second trimester is beneficial. The parents can interrupt the pregnancy. Or, prompt operative treatment after delivery of an infant with this disorder may minimize the development of hypoxemia and acidosis commonly occur in these cases. In addition, appropriate parental counseling may be started.
Downloads
Metrics
References
Benacerraf BR. and Adzick NS. Fetal dia- phragmatic hernia: ultrasound diagnosis and clinical outcome in 19 cases. Obstet Gynecol 1987;156:573-6.
Harrison MR, De lorimier AA. Congenital diaphragmatic hernia. Surg Clin North Am 1981;61:1023-35.
Czeizel A: Schisis-association. Am J Med Genet 1981;10:25-35.
Benjamin DR, Juul S. and Siebert JR. Congenital postero-lateral diaphragmatic hernia: associated malformations. J of Ped Surg 1988;23:899-903.
Stiller RJ, Roberts NS, Weiner S, et al. Congenital diaphragmatic hernia antenatal diagnosis and obstetrical management. J Clin Ultrasound 1985;13:212-5.
Cullen ML, Klein MD and Philippart AI. Congenital diaphragmatic hernia Surg Clin of North Am 1985;65:1115-37.
Adzick NS, Harrison MR, Glick PL. et al. Diaphragmatic hernia in the fetuses: prenatal diagnosis and outcome in 94 cases. J of Ped Surg 1985;20:357-61.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2023 The ASEAN Journal of Radiology
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Disclosure Forms and Copyright Agreements
All authors listed on the manuscript must complete both the electronic copyright agreement. (in the case of acceptance)