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Congenital peritoneal encapsulation of the small intestine: A rare case report

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Autore
Zoulamoglou M., Flessas I., Zarokosta M., Piperos T., Kalles V., Tsiaousis I., Kaklamanos I., Sgantzos M., Mariolis-Sapsakos T.
Data
2016
Language
en
DOI
10.1016/j.ijscr.2016.07.046
Soggetto
abdominal distension
abdominal pain
abdominal scintiscanning
adult
Article
case report
cesarean section
colic
computer assisted tomography
congenital malformation
female
human
laparoscopy
nausea
peritoneal disease
peritoneal encapsulation
peritoneum
priority journal
small intestine disease
small intestine obstruction
Elsevier Ltd
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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. © 2016 The Authors
URI
http://hdl.handle.net/11615/81036
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