Your browser doesn't support javascript.
loading
Congenital pancreatic cyst with Ivemark II syndrome: a rare case.
Chahed, Jamila; Mekki, Mongi; Aloui, Sameh; Hidouri, Saida; Ksia, Amine; Krichène, Imed; Maazoun, Kais; Sahnoun, Lassaad; Belghith, Mohsen; Salem, Randa; Njim, Leila; Nouri, Abdellatif.
Afiliación
  • Chahed J; Pediatric Surgery Department, University Hospital Center of Monastir, 5000 Monastir, Tunisia. j.chahed@voila.fr
J Pediatr Surg ; 47(3): e33-6, 2012 Mar.
Article en En | MEDLINE | ID: mdl-22424375
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.
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Quiste Pancreático / Síndrome de Heterotaxia Tipo de estudio: Diagnostic_studies Límite: Humans / Infant / Male Idioma: En Revista: J Pediatr Surg Año: 2012 Tipo del documento: Article País de afiliación: Túnez
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Quiste Pancreático / Síndrome de Heterotaxia Tipo de estudio: Diagnostic_studies Límite: Humans / Infant / Male Idioma: En Revista: J Pediatr Surg Año: 2012 Tipo del documento: Article País de afiliación: Túnez