中肠扭转合并胃穿孔及静脉周围白质软化一例足月儿

S. Park, J. Hwang
{"title":"中肠扭转合并胃穿孔及静脉周围白质软化一例足月儿","authors":"S. Park, J. Hwang","doi":"10.5385/NM.2021.28.1.53","DOIUrl":null,"url":null,"abstract":"Intestinal malrotation with midgut volvulus (MV) is a life-threatening surgical emer gency. Most events of MV occur in the neonatal period with bilious vomiting, abdominal distension, feeding intolerance, and bloody stools. Neonatal gastric perforation (GP) is a rare and life-threatening condition associated with high mortality. It occurs either in an idiopathic form or in association with gastrointestinal anomalies such as duodenal atresia and MV. The pathogenesis of both MV and GP is related to ischemic change and inflammatory response. MV and GP can lead to morbidities such as sepsis, intestinal ischemia, and organ failure, but not neurologic problems. We herein report the case of a term infant at 5 days after birth, with MV accompanied by GP, who developed periventricular leukomalacia.","PeriodicalId":32945,"journal":{"name":"Neonatal Medicine","volume":"28 1","pages":"53-58"},"PeriodicalIF":0.0000,"publicationDate":"2021-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Case of Midgut Volvulus with Gastric Perforation and Periveintricular Leukomalacia in a Term Infant\",\"authors\":\"S. Park, J. Hwang\",\"doi\":\"10.5385/NM.2021.28.1.53\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Intestinal malrotation with midgut volvulus (MV) is a life-threatening surgical emer gency. Most events of MV occur in the neonatal period with bilious vomiting, abdominal distension, feeding intolerance, and bloody stools. Neonatal gastric perforation (GP) is a rare and life-threatening condition associated with high mortality. It occurs either in an idiopathic form or in association with gastrointestinal anomalies such as duodenal atresia and MV. The pathogenesis of both MV and GP is related to ischemic change and inflammatory response. MV and GP can lead to morbidities such as sepsis, intestinal ischemia, and organ failure, but not neurologic problems. We herein report the case of a term infant at 5 days after birth, with MV accompanied by GP, who developed periventricular leukomalacia.\",\"PeriodicalId\":32945,\"journal\":{\"name\":\"Neonatal Medicine\",\"volume\":\"28 1\",\"pages\":\"53-58\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neonatal Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5385/NM.2021.28.1.53\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neonatal Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5385/NM.2021.28.1.53","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

肠旋转不良伴中肠扭转(MV)是一种危及生命的外科紧急情况。大多数MV发生在新生儿期,伴有胆汁性呕吐、腹胀、进食不耐受和便血。新生儿胃穿孔(GP)是一种罕见且危及生命的高死亡率疾病。它要么以特发性形式发生,要么与十二指肠闭锁和MV等胃肠道异常有关。MV和GP的发病机制都与缺血性变化和炎症反应有关。MV和GP会导致败血症、肠缺血和器官衰竭等疾病,但不会导致神经系统问题。我们在此报告了一例足月婴儿在出生后5天出现室周白质软化症,MV伴GP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
A Case of Midgut Volvulus with Gastric Perforation and Periveintricular Leukomalacia in a Term Infant
Intestinal malrotation with midgut volvulus (MV) is a life-threatening surgical emer gency. Most events of MV occur in the neonatal period with bilious vomiting, abdominal distension, feeding intolerance, and bloody stools. Neonatal gastric perforation (GP) is a rare and life-threatening condition associated with high mortality. It occurs either in an idiopathic form or in association with gastrointestinal anomalies such as duodenal atresia and MV. The pathogenesis of both MV and GP is related to ischemic change and inflammatory response. MV and GP can lead to morbidities such as sepsis, intestinal ischemia, and organ failure, but not neurologic problems. We herein report the case of a term infant at 5 days after birth, with MV accompanied by GP, who developed periventricular leukomalacia.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
17
审稿时长
12 weeks
期刊最新文献
Full-Term Baby with Cerebellar Hemorrhage Referred for Severe Jaundice Occurring within the First 3 Days of Life Should We Consider UGT1A1 Mutation Analysis in Evaluating the Prolonged Jaundice of Newborn Infants? A Case of Oropharyngeal Teratoma Associated with Subluxation of Temporomandibular Joint: A Case Report Does Neonatal Microbiome Research Encompass the Placental Transfer Pathway? Beta Thalassemia Presenting with Neonatal Cholestasis and Extensive Hemosiderosis: A Case Report
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1