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Congenital gastric outlet obstruction by pyloric membrane: prenatal and postnatal diagnosis and management
V. Frisová, L. Kavalcová, M. Kyncl, R. Vlk, A. Kučera, M. Roček
Jazyk angličtina Země Švýcarsko
Typ dokumentu kazuistiky, práce podpořená grantem
NLK
Karger Journals
od 1998-01-01 do 2009
ProQuest Central
od 1998-01-01 do 2015-12-31
Health & Medicine (ProQuest)
od 1998-01-01 do 2015-12-31
PubMed
19816036
DOI
10.1159/000242455
Knihovny.cz E-zdroje
- MeSH
- lidé MeSH
- magnetická rezonanční tomografie MeSH
- obstrukce vyprazdňování žaludku komplikace patologie ultrasonografie MeSH
- polyhydramnion etiologie ultrasonografie MeSH
- těhotenství MeSH
- třetí trimestr těhotenství MeSH
- ultrasonografie prenatální MeSH
- Check Tag
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- kazuistiky MeSH
- práce podpořená grantem MeSH
Congenital gastric outlet obstruction is a rare condition representing only 1% of all gastrointestinal atresias. Prenatal diagnosis is uncommon and mostly confined to the third trimester of cases presenting a combination of polyhydramnios with dilated stomach. We report a case of congenital gastric outlet obstruction by pyloric membrane which was diagnosed prenatally in the third trimester by sonography and magnetic resonance imaging. The anomaly appeared to be isolated, thus a favorable outcome was expected. A baby girl weighing 3,430 g was delivered spontaneously at 36 weeks. Postnatal imaging methods confirmed the presence of a congenital gastric obstruction. 21 h after delivery, the baby underwent laparotomy, at which time a malrotation and pyloric membrane were found and resolved. The postoperative course was uneventful and the baby was discharged at the age of 18 days and remains well at controls.
Citace poskytuje Crossref.org
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- $a Congenital gastric outlet obstruction is a rare condition representing only 1% of all gastrointestinal atresias. Prenatal diagnosis is uncommon and mostly confined to the third trimester of cases presenting a combination of polyhydramnios with dilated stomach. We report a case of congenital gastric outlet obstruction by pyloric membrane which was diagnosed prenatally in the third trimester by sonography and magnetic resonance imaging. The anomaly appeared to be isolated, thus a favorable outcome was expected. A baby girl weighing 3,430 g was delivered spontaneously at 36 weeks. Postnatal imaging methods confirmed the presence of a congenital gastric obstruction. 21 h after delivery, the baby underwent laparotomy, at which time a malrotation and pyloric membrane were found and resolved. The postoperative course was uneventful and the baby was discharged at the age of 18 days and remains well at controls.
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