Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3273910 | Journal de Gynécologie Obstétrique et Biologie de la Reproduction | 2008 | 6 Pages |
Abstract
Usually considered as an isolated malformation carrying a rather good postnatal prognosis, gastroschisis may however occasionally bear an unfavourable outcome despite reassuring ultrasound follow-up. We report on the case of a fetus with gastroschisis diagnosed at 13 weeks of gestation followed by a progressive bowel absorption and closure of the abdominal defect at 24 weeks, associated with a 10 to 15Â mm intra-abdominal bowel tract dilatation. At birth, the infant did not show any recognizable ventral wall defect or scar. Surgical exploration was decided due to the presence of a high level bowel tract occlusion associated with a dilated proximal jejunum on standard abdominal X-ray radiograph. Long-segment atresia of the midintestine without any possible surgical option was observed. The infant died at day 5.
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Authors
C. Foucher, P. Herve, H. Lardy, F. Perrotin,