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

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

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)639-642
Number of pages4
JournalClinical Imaging
Volume36
Issue number5
DOIs
Publication statusPublished - Sep 1 2012

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High-Frequency Ventilation
Extracorporeal Membrane Oxygenation
Inferior Vena Cava
Hernia
Blood Vessels
Stomach
Thorax
Magnetic Resonance Imaging
Congenital Diaphragmatic Hernias

All Science Journal Classification (ASJC) codes

  • Radiology Nuclear Medicine and imaging

Cite this

Ultrasound and MR images of prenatally diagnosed bilateral congenital diaphragmatic hernia, a rare variation of CDH. / Hiasa, Kana; Fujita, Yasuyuki; Fukushima, Kotaro; Nagata, Kouji; Taguchi, Tomoaki; Wake, Norio.

In: Clinical Imaging, Vol. 36, No. 5, 01.09.2012, p. 639-642.

Research output: Contribution to journalArticle

Hiasa, Kana ; Fujita, Yasuyuki ; Fukushima, Kotaro ; Nagata, Kouji ; Taguchi, Tomoaki ; Wake, Norio. / Ultrasound and MR images of prenatally diagnosed bilateral congenital diaphragmatic hernia, a rare variation of CDH. In: Clinical Imaging. 2012 ; Vol. 36, No. 5. pp. 639-642.
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