| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4157472 | Journal of Pediatric Surgery | 2012 | 4 Pages |
Abstract
An infant with congenital pancreatic cyst with Ivemark II syndrome is reported because it is a rare association. The infant had associated situs inversus, asplenia, and complex congenital heart disease. The pancreatic cyst was successfully managed by cystoduodenostomy because of connection to the biliary tract. The infant succumbed as a result of heart failure at age 2 months. Prognosis depends on the presence of life-threatening malformations.
Keywords
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Perinatology, Pediatrics and Child Health
Authors
Jamila Chahed, Mongi Mekki, Sameh Aloui, Saida Hidouri, Amine Ksia, Imed Krichène, Kais Maazoun, Lassaad Sahnoun, Mohsen Belghith, Randa Salem, Leila Njim, Abdellatif Nouri,