Use of ultrasound and MRI for evaluation of lung volumes in fetuses with isolated left congenital diaphragmatic hernia

被引：23
|
作者：
Victoria, Teresa [1 ,2 ]
Danzer, Enrico [2 ]
Adzick, N. Scott [2 ]
机构：
[1] Childrens Hosp Philadelphia, Dept Radiol, Philadelphia, PA 19103 USA
[2] Childrens Hosp Philadelphia, Ctr Fetal Diag & Treatment, Philadelphia, PA 19103 USA
来源：
SEMINARS IN PEDIATRIC SURGERY | 2013年 / 22卷 / 01期
关键词：
Congenital diaphragmatic hernia; Fetal MRI; LHR; O/E fetal lung volume; ENDOSCOPIC TRACHEAL OCCLUSION; TO-HEAD RATIO; MAGNETIC-RESONANCE; LIVER HERNIATION; STOMACH POSITION; PROGNOSTIC VALUE; PREDICTION; SURVIVAL; AREA; HYPOPLASIA;
D O I：
10.1053/j.sempedsurg.2012.10.006
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Congenital diaphragmatic hernia (CDH) is an anomaly that results in lung hypoplasia and pulmonary hypertension. The lungs of the CDH fetus have an abnormal architecture, with fewer bronchial branches and decreased number of arteries and veins, factors which result in pulmonary compromise postnatally. The goal of this review is to evaluate prenatal prognostic factors in the fetus with isolated left CDH, with particular emphasis on fetal MRI. These imaging indicators may be used to provide health professionals and the parents with the most accurate information about fetal prognosis. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码：30 / 36
页数：7
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