[Oesophageal duplication with neonatal revelation. About 2 cases]

Autor: L, Karboubi, N, Sadiq, M, Kisra, M, Kabiri, A, Barkat, F, Ettaybi, N L, Bouazzaoui
Jazyk: francouzština
Rok vydání: 2007
Předmět:
Zdroj: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 15(8)
ISSN: 0929-693X
Popis: Oesophageal duplication is a rare form of digestive duplication. This congenital malformation can be asymptomatic or manifest itself through respiratory signs due to airway compression. We report 2 cases of oesophageal duplication discovered in the neonatal period.In both cases, symptoms were dominated by respiratory distress and vomiting. Diagnosis was confirmed by oesophageal contrast X-rays, which revealed a total tubular form in the 1st case and a cystic form in the 2nd case.Oesophageal duplication is a rare abnormality of benign nature, which can be revealed in neonatal period by a noisy compression picture. Diagnosis of this anomaly should trigger a search for other digestive duplications, as well as associated malformations, in particular vertebral.
Databáze: OpenAIRE