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一例极其罕见的产前诊断为主动脉瓣和肺动脉瓣均缺失的病例。

An extremely rare case of prenatally diagnosed absent both aortic and pulmonary valves.

作者信息

Yeon Hyeon Kyeong, Lee Mi-Young, Yoon Sun-Young, Jung Hee Jung, Park Ji Eun, Shim Jae-Yoon, Won Hye-Sung, Lee Pil-Ryang, Kim Ahm

机构信息

Department of Obstetrics and Gynecology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.

出版信息

Obstet Gynecol Sci. 2016 Sep;59(5):393-6. doi: 10.5468/ogs.2016.59.5.393. Epub 2016 Sep 13.

Abstract

We describe a case of absent aortic and pulmonary valves, diagnosed at 16.4 weeks of gestation. Fetal echocardiography showed cardiomegaly with dilated both ventricles. No valve leaflets were observed in the aorta and pulmonary artery, and a typical to-and-fro flow pattern was noted in both great arteries on color Doppler imaging. Fetal hydrops was also detected. Follow-up ultrasonographic evaluation at 19 weeks demonstrated intrauterine fetal death. Postmortem autopsy revealed the absence of both aortic and pulmonary valve leaflets. To the best of our knowledge, this is the earliest diagnosed case of absent both aortic and pulmonary valves and only the second case to be diagnosed prenatally.

摘要

我们描述了一例在妊娠16.4周时被诊断出的主动脉瓣和肺动脉瓣缺如病例。胎儿超声心动图显示心脏增大,双心室扩张。在主动脉和肺动脉中未观察到瓣膜小叶,彩色多普勒成像显示两条大动脉均有典型的往返血流模式。还检测到胎儿水肿。19周时的超声随访评估显示宫内胎儿死亡。尸检显示主动脉瓣和肺动脉瓣小叶均缺如。据我们所知,这是最早诊断出的主动脉瓣和肺动脉瓣均缺如的病例,也是第二例产前诊断的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5d8/5028647/8c3ad34c34cb/ogs-59-393-g001.jpg

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