Cantrell五联症合并心异位1例。

IF 1.7 Q2 PEDIATRICS
Pediatric health, medicine and therapeutics Pub Date : 2022-08-15 eCollection Date: 2022-01-01 DOI:10.2147/PHMT.S374289
Muneer Fazea, Mansour Alhameli, Faisal Ahmed, Mohammad Reza Askarpour, Wafa Murshed, Azizh Jarwsh, Amal Alkbous
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引用次数: 2

摘要

Cantrell五联症是一种中间中胚层结构的先天性异常,预后较差。它的特点是前膈、胸骨下段、腹壁、心包缺损和各种先天性心脏畸形。我们报告一例心脏异位和Cantrell五联症在一个健康的35岁妇女,没有胚胎毒性暴露史或吸烟的新生儿。这名婴儿在妊娠中期首次被诊断出患有这种异常,并在孕35周时通过剖腹产分娩。出生后不久,由于进行性呼吸衰竭,他被转移到新生儿重症监护病房(NICU),最终,与败血症一起,导致婴儿在第二天死亡。总之,应适当评估Cantrell五联症,以便与多学科团队进行有效的产前咨询和产后管理;由于婴儿生存评估和早期诊断给父母终止妊娠的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pentalogy of Cantrell Associated with Ectopia Cordis: A Case Report.

Pentalogy of Cantrell Associated with Ectopia Cordis: A Case Report.

Pentalogy of Cantrell Associated with Ectopia Cordis: A Case Report.

Pentalogy of Cantrell Associated with Ectopia Cordis: A Case Report.

Pentalogy of Cantrell is a congenital anomaly of the median mesodermal constructions with a poor prognosis. It is characterized by defects of the anterior diaphragm, the lower sternum, the abdominal wall, pericardium, and various congenital heart malformations. We present a case of ectopia cordis and Pentalogy of Cantrell in a newborn of a healthy 35-year-old woman with no history of embryotoxic exposure or smoking. The infant was first diagnosed with the anomaly in the second trimester of pregnancy and was delivered at 35 weeks of gestational age via a caesarian section. Shortly after birth, he was transferred to the neonatal intensive care unit (NICU) due to progressive respiratory failure, which ultimately, along with septicemia, led to infant death on the second day. In conclusion, the Pentalogy of Cantrell should be appropriately assessed for effective prenatal counseling and postnatal management with a multidisciplinary team; since infant survival assessment and early diagnosis give the parents the option of terminating the pregnancy.

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