Citation:
Zoulamoglou M, Flessas I, Zarokosta M, Piperos T, Kalles V, Tsiaousis I, Kaklamanos I, Sgantzos M, Mariolis-Sapsakos T. Congenital peritoneal encapsulation of the small intestine: A rare case report. Int J Surg Case Rep. 2016;27:28-31.
Abstract:
INTRODUCTION: Peritoneal Encapsulation (PE) is a scarce congenital malformation, characterized by a supplementary peritoneal membrane that covers all or a part of the small intestine.
PRESENTATION OF CASE: PE was unexpectantly discovered in a young woman during laparotomy for bowel obstruction. There were no specific pre-operative indications of this malformation. The operation was uneventful.
DISCUSSION: PE is a very rare congenital anatomical anomaly that is difficultly identified pre-operatively. PE is mainly asymptomatic, but in some cases, like in the presented one, PE presents with small bowel obstruction. Surgeons should be aware of this malformation and suspect it when encountering a patient with small bowel obstruction without other etiological factors.
CONCLUSION: Knowledge of this peculiar congenital anomaly is pivotal, so that accurate diagnosis and appropriate management of it are direct and efficient.