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足月新生儿的坎特雷尔五联症

Pentalogy of Cantrell in Full Term Neonate.

作者信息

Taee Nadereh, Goodarzi Mojgan Faraji, Safdari Mohammad, Bajelan Amir

机构信息

Department of Pediatrics, Lorestan University of Medical Sciences, Khorramabad, Iran.

Medical Student, Lorestan University of Medical Sciences, Khorramabad, Iran.

出版信息

AJP Rep. 2019 Apr;9(2):e144-e146. doi: 10.1055/s-0039-1683936. Epub 2019 Apr 9.

Abstract

Pentalogy of Cantrell (PC) is an uncommon congenital disorder characterized by severe defects in the chest and abdomen, including abdominal visceral prolapsed via umbilical cord (omphalocele), defect in the lower part of the sternum, defect in the front of the diaphragm, defects in the anterior part of the pericardium, and the ectopiacordis. Here, we report a 2-hour-old girl, weighing 3,500 g, who was referred to Shahid Madani Hospital in Khorramabad due to the large omphalocele on her chest with pulsating mass above it. The baby was the first child of a 24-year-old mother who was born with an uncomplicated vaginal delivery. Very rare cases of PC are born as a term new-born.

摘要

坎特雷尔五联症(PC)是一种罕见的先天性疾病,其特征为胸部和腹部存在严重缺陷,包括经脐带的腹腔脏器脱垂(脐膨出)、胸骨下部缺损、膈肌前部缺损、心包前部缺损以及心脏异位。在此,我们报告一名2小时大的女婴,体重3500克,因胸部巨大脐膨出且上方有搏动性肿块被转诊至霍拉马巴德的沙希德·马达尼医院。该婴儿是一名24岁母亲的头胎,母亲顺产,分娩过程无并发症。PC极为罕见,该婴儿为足月儿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca38/6456328/489886ac36c3/10-1055-s-0039-1683936-i180027-1.jpg

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