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Tracheobronchomegaly following intrauterine tracheal occlusion for congenital diaphragmatic hernia

机译:宫腔内气管闭塞后先天性diaphragm肌疝气管支气管扩张

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摘要

Fetuses with severe congenital diaphragmatic hernia (CDH) and pulmonary hypoplasia may benefit from fetal endoluminal tracheal occlusion (FETO). Enlargement of the main bronchi and trachea appears to be a common complication of FETO.
机译:患有严重先天性diaphragm肌疝(CDH)和肺发育不全的胎儿可能会受益于胎儿腔内气管阻塞(FETO)。主支气管和气管增大似乎是FETO的常见并发症。

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  • 来源
    《Pediatric Radiology》 |2012年第8期|p.916-922|共7页
  • 作者单位

    Department of Pediatric Radiology, Hospital Universitario Vall d’Hebron - AMI, Ps. Vall d’Hebron 119-129, 08035, Barcelona, Spain;

    Department of Pediatric Radiology, Hospital Universitario Vall d’Hebron - AMI, Ps. Vall d’Hebron 119-129, 08035, Barcelona, Spain;

    Department of Pediatric Radiology, Hospital Universitario Vall d’Hebron - AMI, Ps. Vall d’Hebron 119-129, 08035, Barcelona, Spain;

    Department of Pediatric Radiology, Hospital Universitario Vall d’Hebron - AMI, Ps. Vall d’Hebron 119-129, 08035, Barcelona, Spain;

    Department of Pediatric Radiology, Hospital Universitario Vall d’Hebron - AMI, Ps. Vall d’Hebron 119-129, 08035, Barcelona, Spain;

    Department of Pediatric Surgery, Hospital Universitario Vall d’Hebron, Barcelona, Spain;

    Department of Obstetrics and Gynecology, Hospital Universitario Vall d’Hebron, Barcelona, Spain;

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

    Tracheobronchomegaly; Fetal endoluminal tracheal occlusion; Congenital diaphragmatic hernia; Lung hypoplasia;

    机译:气管支气管肿大;胎儿腔内气管闭塞;先天性diaphragm疝;肺发育不全;

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