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胎儿空肠闭锁的产前诊断:一例报告

Prenatal Diagnosis of Fetal Jejunal Atresia: A Case Report.

作者信息

Galani Apostolia, Zikopoulos Athanasios, Papandreou Lampros, Mastora Eirini, Zikopoulos Konstantinos, Makrydimas George

机构信息

Obstetrics and Gynaecology, University Hospital of Ioannina, Ioannina, GRC.

Obstetrics and Gynaecology, Royal Cornwall Hospital, Cornwall, GBR.

出版信息

Cureus. 2021 Oct 21;13(10):e18947. doi: 10.7759/cureus.18947. eCollection 2021 Oct.

Abstract

Intestinal atresia is the result of fetal bowel maldevelopment which leads to congenital bowel obstruction. It is a common cause of ileus of the newborn and can occur at any site of the gastrointestinal tract. Prenatal diagnosis relies on the demonstration of dilated loops of the fetal bowel and the presence of polyhydramnios at the end of the second or more frequently the third trimester of pregnancy. This condition requires surgical correction soon after birth, with timely diagnosis improving the prognosis. Here, we present the case of a fetus diagnosed with jejunal atresia at 33weeks of pregnancy.

摘要

肠闭锁是胎儿肠道发育异常导致的先天性肠梗阻。它是新生儿肠梗阻的常见原因,可发生于胃肠道的任何部位。产前诊断依赖于妊娠中期(多为妊娠晚期)超声显示胎儿肠管扩张及羊水过多。这种情况需要在出生后尽快进行手术矫正,及时诊断可改善预后。在此,我们报告一例在妊娠33周时被诊断为空肠闭锁的胎儿病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e2/8605830/e37ea4f39726/cureus-0013-00000018947-i01.jpg

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