Peculiar type 1 congenital pyloric atresia: a case report
<p>Abstract</p> <p>Pyloric atresia (PA) is a very rare condition. Its incidence is approximately 1 in 100,000 newborns and constitutes about 1% of all intestinal atresias. We describe the neonatal course of a peculiar case of type 1 pyloric atresia, in which the pyloric membrane wa...
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2010-01-01T00:00:00Z.
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| 001 | doaj_8d7460eb93a541e9925a85d6903cb99b | ||
| 042 | |a dc | ||
| 100 | 1 | 0 | |a Nanni Lorenzo |e author |
| 700 | 1 | 0 | |a Pintus Claudio |e author |
| 700 | 1 | 0 | |a Corsello Mirta |e author |
| 700 | 1 | 0 | |a Zecca Enrico |e author |
| 700 | 1 | 0 | |a Zecca Susanna |e author |
| 245 | 0 | 0 | |a Peculiar type 1 congenital pyloric atresia: a case report |
| 260 | |b BMC, |c 2010-01-01T00:00:00Z. | ||
| 500 | |a 10.1186/1824-7288-36-3 | ||
| 500 | |a 1720-8424 | ||
| 500 | |a 1824-7288 | ||
| 520 | |a <p>Abstract</p> <p>Pyloric atresia (PA) is a very rare condition. Its incidence is approximately 1 in 100,000 newborns and constitutes about 1% of all intestinal atresias. We describe the neonatal course of a peculiar case of type 1 pyloric atresia, in which the pyloric membrane was connected to a second duodenal membrane through a virtual duodenal lumen in a premature newborn. The atypical variant required an unusual side to side gastroduodenostomy. We emphasize the importance of a prompt diagnosis to avoid potentially fatal complications and to warrant a good outcome even in the presence of a strange form of PA in the neonatal period.</p> | ||
| 546 | |a EN | ||
| 690 | |a Pediatrics | ||
| 690 | |a RJ1-570 | ||
| 655 | 7 | |a article |2 local | |
| 786 | 0 | |n Italian Journal of Pediatrics, Vol 36, Iss 1, p 3 (2010) | |
| 787 | 0 | |n http://www.ijponline.net/content/36/1/3 | |
| 787 | 0 | |n https://doaj.org/toc/1720-8424 | |
| 787 | 0 | |n https://doaj.org/toc/1824-7288 | |
| 856 | 4 | 1 | |u https://doaj.org/article/8d7460eb93a541e9925a85d6903cb99b |z Connect to this object online. |