首页> 美国卫生研究院文献>Journal of the Belgian Society of Radiology >An Unusual Presentation of Congenital Esophageal Stenosis Due toTracheobronchial Remnants in a Newborn Prenatally Diagnosed with DuodenalAtresia
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An Unusual Presentation of Congenital Esophageal Stenosis Due toTracheobronchial Remnants in a Newborn Prenatally Diagnosed with DuodenalAtresia

机译:先天性食管狭窄的异常表现新生儿产前经十二指肠气管支气管残余物的诊断闭锁

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摘要

Congenital esophageal stenosis due to tracheobronchial remnants is defined as an intrinsic stenosis of the esophagus caused by congenital architectural abnormalities of the esophageal wall. Although CES is present at birth, it remains asymptomatic till at the age of 4–10 months, when solid food is introduced. Here we present a case diagnosed in the neonatal period after urgent cesarean for an associated duodenal atresia complicated with perforation. There is a mutual association between duodenal atresia and congenital esophageal stenosis. When duodenal atresia is diagnosed, think of possible associated esophageal abnormalities, especially when duodenal atresia is complicated by gastric perforation prenatally.
机译:由气管支气管残余物引起的先天性食管狭窄被定义为由食管壁的先天性建筑异常引起的食管固有狭窄。尽管CES在出生时就存在,但在引入固体食物之前,它直到4-10个月大都没有症状。在这里,我们介绍一例在紧急剖腹产后伴发十二指肠闭锁并穿孔的新生儿。十二指肠闭锁与先天性食管狭窄之间存在相互联系。当诊断出十二指肠闭锁时,请考虑可能的相关食道异常,尤其是当十二指肠闭锁并发于产前胃穿孔时。

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