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Prenatal diagnosis of bilateral diaphragmatic hernia by fetal sonography
Derya Eroglu 1 , Filiz Yanik 1 , Ayse Ebru Sakallioglu 2 , Unser Arikan 3 , Birgul Varan 4 and Esra Kuscu 1
 Departments of 1Obstetrics and Gynecology,   2 Pediatric Surgery,   3 Pathology and   4 Pediatric Cardiology, Baskent University School of Medicine, Ankara, Turkey
Correspondence to  Dr Derya Eroglu, Baskent University School of Medicine, Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Kubilay Sok. No: 36 Maltepe, TR-06570 Ankara, Turkey. Email: d_eroglu@hotmail.com
Copyright 2006 Japan Society of Obstetrics and Gynecology
KEYWORDS
bilateral congenital diaphragmatic hernia • fetal sonography • lung hypoplasia • postnatal outcome • prenatal diagnosis

Abstract

AbstractIntroductionCase ReportDiscussionReferences

This report describes a case of prenatally diagnosed bilateral diaphragmatic hernia. At 22 weeks' gestation, ultrasound revealed a cystic structure behind the fetus's heart on the axial image at the level of the cardiac four-chamber view. This suggested a left-sided congenital diaphragmatic hernia with herniation of the stomach into the left hemithorax. However, the left-to-right midline shift of the heart was minimal, which is not typical of left-sided congenital diaphragmatic hernia. Throughout the 30th week of gestation, the right and left branches of the pulmonary artery were hypoplastic compared with the values in normal fetuses of the same gestational age. The presumptive diagnosis was bilateral congenital diaphragmatic hernia. A female newborn weighing 2900 g was delivered at 37 weeks' gestation, and she died at 7 h of age. An autopsy revealed large defects on both sides of the diaphragm. In conclusion, prenatal diagnosis of bilateral diaphragmatic hernia is possible with fetal sonography.


Received: April 22 2005.
Accepted: October 28 2005.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1447-0756.2006.00357.x About DOI

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