Outcome of congenital cystic adenomatoid malformation of the lung after antenatal diagnosis

被引：22

作者：

Hsieh, CC ^{[1
]}

Chao, AS ^{[1
]}

Chang, YL ^{[1
]}

Kuo, DM ^{[1
]}

Hsieh, TT ^{[1
]}

Hung, HT ^{[1
]}

机构：

[1] Chang Gung Mem Hosp, Dept Obstet & Gynecol, Div Maternal Fetal Med, Taipei 105, Taiwan

来源：

INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS | 2005年 / 89卷 / 02期

关键词：

prenatal diagnosis; outcome; congenital anomalies; congenital cystic adenomatoid malformation of the lung;

D O I：

10.1016/j.ijgo.2004.11.031

中图分类号：

R71 [妇产科学];

学科分类号：

100211 ;

摘要：

Objective: We evaluated the outcome of fetuses diagnosed with having congenital cystic adenomatoid malformation (CCAM) on ultrasonographic examination and managed conservatively. Methods: A retrospective study of 19 cases of CCAM diagnosed antenatatty in our hospital was conducted between 1990 and 2001. Complete clinical information was available for all patients, with a mean follow-up of 62 months. Results: The median gestational age at which CCAM was diagnosed was 23 weeks and there were eight live births. With conservative postnatal management, seven neonates had no major complications and one developed bronchopneumonia. Conclusion: Taken together, the findings of the present study and a review of the literature strongly support the conservative management of selected neonates with CCAM. (c) 2005 International Federation of Gynecology and Obstetrics. Published by Elsevier Ireland Ltd. All rights reserved.

引用

页码：99 / 102

页数：4

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