Ultrasound and MR images of prenatally diagnosed bilateral congenital diaphragmatic hernia, a rare variation of CDH

Kana Ishibashi Hiasa, Yasuyuki Fujita, Kotaro Fukushima, Kouji Nagata, Tomoaki Taguchi, Norio Wake

研究成果: Contribution to journalArticle査読

3 被引用数 (Scopus)

抄録

The patient referred to our hospital at 29 weeks. The detailed ultrasound study demonstrated the stomach behind the heart, the slight deviation of the heart, and the vascular connection between the right chest organ and inferior vena cava. Bilateral congenital diaphragmatic hernia was suggested and confirmed by magnetic resonance imaging. A baby was delivered at 37 weeks and immediately placed on high-frequency oscillation ventilation. Although a surgical correction of the bilateral hernia under extracorporeal membrane oxygenation was completed, he expired at 14 h of age.

本文言語英語
ページ(範囲)639-642
ページ数4
ジャーナルClinical Imaging
36
5
DOI
出版ステータス出版済み - 9 2012

All Science Journal Classification (ASJC) codes

  • Radiology Nuclear Medicine and imaging

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