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Neonatal Congenital Pancreatic Cyst: A Report of Three Cases | OMICS International | Abstract

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Case Report

Neonatal Congenital Pancreatic Cyst: A Report of Three Cases

Chahed Jamila1*, Kechiche Nahla1, Hidouri Saida1, Aloui Sameh1, Ksia Amine1, Mekki Mongi1, Sahnoun Lassad1, Krichene Imed1, Belghith Mohsen1, Zakhama Abdelfatteh2, Salem Randa3 and Nouri Abdellatif1
1Paediatric Surgery Department of EPS Fattouma Bourguiba, Tunisia
2Department of Histopathology of EPS Fattouma Bourguiba, Tunisia
3Department of Radiology of EPS Fattouma Bourguiba, Tunisia
Corresponding Author : Chahed Jamila
Pediatric Surgery Department of EPS Monastir CP 5000
Research laboratory LR 12SP13, School of medicine of Monastir
University of Monastir, Tunisia
Tel: +21673461144
Fax: +21673460678
E-mail: j.chahed@voila.fr
Received June 11, 2014; Accepted July 15, 2015; Published July 20, 2015
Citation: Jamila C, Nahla K, Saida H, Sameh A, Amine K, et al. (2015) Neonatal Congenital Pancreatic Cyst: A Report of Three Cases. J Preg Child Health 2:179. doi: 10.4172/2376-127X.1000179
Copyright: © 2015 Jamila C, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Neonatal congenital pancreatic cyst is rare. It can be isolated or associated to other malformations. Early management is recommended because of possible severe complications. The aim of our work is to report our experience with three newborns with congenital pancreatic cyst. A five year (2010-2015) retrospective study is carried. Data were collected from medical files of three different patients. Diagnosis was prenatal in two patients. The Cyst was associated to Ivemark syndrome in two cases and solitary in one. Cystic complications were infection in one case and pancreatitis with liver cirrhosis in another case. These pancreatic cysts were successfully managed by surgery. One patient succumbed as a result of heart failure. To our knowledge we report the first case of congenital pancreatic cyst complicated with liver cirrhosis. We concluded that prompt diagnosis is important to prevent severe complications. Prognosis is dependent on early management and on life threatening associated malformations.

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