TY - JOUR
T1 - Ultrasound and MR images of prenatally diagnosed bilateral congenital diaphragmatic hernia, a rare variation of CDH
AU - Hiasa, Kana Ishibashi
AU - Fujita, Yasuyuki
AU - Fukushima, Kotaro
AU - Nagata, Kouji
AU - Taguchi, Tomoaki
AU - Wake, Norio
PY - 2012/9
Y1 - 2012/9
N2 - 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.
AB - 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.
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U2 - 10.1016/j.clinimag.2011.11.033
DO - 10.1016/j.clinimag.2011.11.033
M3 - Article
C2 - 22920382
AN - SCOPUS:84865361360
VL - 36
SP - 639
EP - 642
JO - Clinical Imaging
JF - Clinical Imaging
SN - 0899-7071
IS - 5
ER -