• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Type I fetal cystic adenomatoid malformation of the lung with hydrops at 18 weeks' gestation: a case report.

作者信息

Lagrew D C, Morgan M A, Branigan T, Lee T, Randall R

机构信息

Saddleback Memorial Medical Center, Laguna Hills, Calif.

出版信息

J Perinatol. 1994 Jul-Aug;14(4):316-8.

PMID:7965230
Abstract

Fetal cystic adenomatoid malformation, type I, is a rare pulmonary anomaly that has been diagnosed after 20 weeks' gestation. The prognosis of this malformation is usually dependent on whether it is microcystic, types II and III, or macrocystic, type I. We report a case of severe macrocystic fetal cystic adenomatoid malformation diagnosed at 18.4 weeks' gestation. This case demonstrates that fetal cystic adenomatoid malformation can be diagnosed at 18 weeks and that hydrops with oligohydramnios may be part of the natural history of type I lesions this early in pregnancy.

摘要

相似文献

1
Type I fetal cystic adenomatoid malformation of the lung with hydrops at 18 weeks' gestation: a case report.
J Perinatol. 1994 Jul-Aug;14(4):316-8.
2
Nonimmune fetal hydrops caused by bilateral type III congenital cystic adenomatoid malformation of the lung at 17 weeks' gestation.孕17周时由双侧III型先天性肺囊性腺瘤样畸形引起的非免疫性胎儿水肿。
Am J Obstet Gynecol. 1992 Aug;167(2):503-5. doi: 10.1016/s0002-9378(11)91438-0.
3
Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature.导致胎儿水肿的肺囊性腺瘤样畸形:病例报告及文献复习
Arch Gynecol Obstet. 2009 Aug;280(2):293-6. doi: 10.1007/s00404-008-0880-4. Epub 2008 Dec 20.
4
Fetal lung lesions: management and outcome.胎儿肺部病变:管理与结局
Am J Obstet Gynecol. 1998 Oct;179(4):884-9. doi: 10.1016/s0002-9378(98)70183-8.
5
Antenatal intervention for congenital cystic adenomatoid malformation.
Lancet. 1990 Oct 20;336(8721):965-7. doi: 10.1016/0140-6736(90)92420-m.
6
Successful outcome in a case of cystic adenomatoid malformation of the lung complicated by fetal hydrops, using extracorporeal membrane oxygenation.应用体外膜肺氧合治疗合并胎儿水肿的肺囊性腺瘤样畸形患儿取得成功。
Fetal Diagn Ther. 1994 Mar-Apr;9(2):88-91. doi: 10.1159/000263914.
7
Spontaneous resolution of nonimmune hydrops in a fetus with a cystic adenomatoid malformation.
J Perinatol. 1998 Jul-Aug;18(4):308-10.
8
Fetal case of congenital cystic adenomatoid malformation of the lung: fetal therapy and a review of the published reports in Japan.胎儿先天性肺囊性腺瘤样畸形病例:胎儿治疗及日本已发表报告综述
Congenit Anom (Kyoto). 2005 Sep;45(3):96-101. doi: 10.1111/j.1741-4520.2005.00075.x.
9
Successful thoracoamniotic shunting using a double-flower catheter in a case of fetal cystic adenomatoid malformation associated with hydrops and polyhydramnios.在一例与水肿和羊水过多相关的胎儿囊性腺瘤样畸形病例中,使用双花导管成功进行胸腔羊膜分流术。
Ultrasound Obstet Gynecol. 1997 Oct;10(4):293-6. doi: 10.1046/j.1469-0705.1997.10040293.x.
10
Prenatal diagnosis of congenital cystic adenomatoid lung malformation: a report of seven cases.
Prenat Diagn. 1993 Jan;13(1):65-71. doi: 10.1002/pd.1970130110.