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A rare type of ileal atresia due to intrauterine intussusception

机译:宫腔套叠引起的一种罕见的回肠闭锁

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摘要

Intrauterine intussusception is an extremely rare cause of intestinal atresia. We report on a full-term neonate with clinical manifestations of intestinal obstruction two days after birth. The prenatal sonography at the late stage of pregnancy did not show any abnormality. The barium enema suggested distal intestinal obstruction. At surgery, a visible ileo-ileal intussusception resulting in ileal atresia was found. According to our knowledge, this presentation of ileal atresia did not fit into the present classification and have not yet been reported on. We present this rare type of ileal atresia due to intrauterine intussusception with operative evidence, which is the first case reported in the medical literature so far.
机译:子宫内肠套叠是肠道闭锁的极为罕见的原因。我们报告了足月新生儿,出生后两天有肠梗阻的临床表现。妊娠后期的产前超声检查未显示任何异常。钡灌肠提示远端肠梗阻。在手术中,发现可见的回肠肠套叠,导致回肠闭锁。据我们所知,这种回肠闭锁的表现不适合目前的分类,尚未有报道。我们提出了这种由于宫腔内肠套叠而引起的回肠闭锁的罕见类型,并有手术证据,这是迄今为止医学文献中首次报道的病例。

著录项

  • 来源
    《European Journal of Pediatrics 》 |2007年第11期| 1177-1178| 共2页
  • 作者单位

    Department of Pediatrics National Defense Medical Center Taipei Taiwan People’s Republic of China;

    Department of Pediatric Surgery Tri-Service General Hospital National Defense Medical Center No. 325 Cheng-Kung Rd. Sec. 2 Neihu Taipei 114 Taiwan People’s Republic of China;

    Department of Pediatrics National Defense Medical Center Taipei Taiwan People’s Republic of China;

    Department of Pediatric Surgery Tri-Service General Hospital National Defense Medical Center No. 325 Cheng-Kung Rd. Sec. 2 Neihu Taipei 114 Taiwan People’s Republic of China;

    Department of Pediatric Surgery Tri-Service General Hospital National Defense Medical Center No. 325 Cheng-Kung Rd. Sec. 2 Neihu Taipei 114 Taiwan People’s Republic of China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Ileal atresia; Intrauterine intussusception;

    机译:回肠闭锁;宫腔套叠;

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