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CASE REPORT Open Access An asymptomatic case of peritoneal encapsulation: case report and review of the literature Omer S Al-Taan, Martyn D Evans * , Javid A Shami Abstract Peritoneal encapsulation is a rare congenital anomaly characterised by a thin membrane of peritoneum encasing the small bowel to form an accessory peritoneal sac. We present a case of peritoneal encapsulation diagnosed inci- dentally in an 82 year old man undergoing laparotomy for colonic cancer. The sac was easily excised and surgery was otherwise uneventful. A discussion of the case and a review of the literature are presented. Introduction Peritoneal encapsulation (PE) is a very rare condition that is characterised by a thin membrane encasing the small bowel forming an accessory peritoneal sac. Cases usually present with small bowel obstruction or can be an incidental finding during laparotomy. We present a case of PE diagnosed during surgery for a colon cancer. Case report An 82 year old white male presented to the out patient clinic complaining of left iliac fossa pain and was diag- nosed with a descending colon cancer. He had never undergone abdominal surgery previously. The tumour was thought to be at risk of obstructing the colon and a potentially curative surgery was planned. During opera- tion and after entering the peritoneal cavity the small bowel was entirely covered with a thin membrane that had the appearance of an accessory peritoneum through which the small bowels were visible (see figure 1, figure 2, figure 3 and figure 4). Excision of the membrane released the small bowels. There was no associated small bowel pathology or adhesions. A palliative Hart- manns procedure was performed as peritoneal metas- tases were encountered during surgery. The patient made a good recovery post operatively and was dis- charged from hospital after five days. Discussion Peritoneal encapsulation is a very rare condition charac- terised by what looks to be an accessory peritoneal membrane covering all or part of the small bowels [1]. This is attached to the ascending and descending colon laterally, the transverse colon superiorly and the poster- ior surface of the parietal peritoneum inferiorly. It is believed to be caused by mal-rotation of the bowel dur- ing the 12 th week of gestation [1], this causes the forma- tion of an accessory sac from the peritoneum covering the umbilicus. The membrane may cover the entire or part of the small bowel from the duodeno-jejunal junc- tion down to the ileo-colic junction [2]. The two commonest clinical presentations are: acute small bowel obstruction or incidental diagnosis during laparotomy for another condition [4], however, many cases are incidental findings at autopsy. Some patients may have episodes of intermittent colicky abdominal pain or episodes or sub-acute small bowel obstruction, prior to a definitive diagnosis, Diagnosis of PE pre-operatively may be impossible because plain abdominal x-ray may be normal or only show dilated small bowel loop and CT scan findings can be very non-specific [3]. Membrane division during sur- gery is curative (assuming there is no ischaemic bowel) [2]. On literature search no re-operation was reported on PE after dividing the encasing membrane. Knowledge of this congenital anomaly is of potential use to the abdominal surgeon, as its presence is not reported in standard anatomical descriptions. Its pre- sence is a source of potential confusion, particularly in * Correspondence: [email protected] General Surgery Department, Princess of Wales Hospital, (Coity Road), Bridgend, (CF31 1PU), UK Al-Taan et al. Cases Journal 2010, 3:13 http://www.casesjournal.com/content/3/1/13 © 2010 Al-Taan et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • CASE REPORT Open Access

    An asymptomatic case of peritonealencapsulation: case report and review of theliteratureOmer S Al-Taan, Martyn D Evans*, Javid A Shami

    Abstract

    Peritoneal encapsulation is a rare congenital anomaly characterised by a thin membrane of peritoneum encasingthe small bowel to form an accessory peritoneal sac. We present a case of peritoneal encapsulation diagnosed inci-dentally in an 82 year old man undergoing laparotomy for colonic cancer. The sac was easily excised and surgerywas otherwise uneventful. A discussion of the case and a review of the literature are presented.

    IntroductionPeritoneal encapsulation (PE) is a very rare conditionthat is characterised by a thin membrane encasing thesmall bowel forming an accessory peritoneal sac. Casesusually present with small bowel obstruction or can bean incidental finding during laparotomy. We present acase of PE diagnosed during surgery for a colon cancer.

    Case reportAn 82 year old white male presented to the out patientclinic complaining of left iliac fossa pain and was diag-nosed with a descending colon cancer. He had neverundergone abdominal surgery previously. The tumourwas thought to be at risk of obstructing the colon and apotentially curative surgery was planned. During opera-tion and after entering the peritoneal cavity the smallbowel was entirely covered with a thin membrane thathad the appearance of an accessory peritoneum throughwhich the small bowels were visible (see figure 1, figure2, figure 3 and figure 4). Excision of the membranereleased the small bowels. There was no associatedsmall bowel pathology or adhesions. A palliative Hart-mann’s procedure was performed as peritoneal metas-tases were encountered during surgery. The patientmade a good recovery post operatively and was dis-charged from hospital after five days.

    DiscussionPeritoneal encapsulation is a very rare condition charac-terised by what looks to be an accessory peritonealmembrane covering all or part of the small bowels [1].This is attached to the ascending and descending colonlaterally, the transverse colon superiorly and the poster-ior surface of the parietal peritoneum inferiorly. It isbelieved to be caused by mal-rotation of the bowel dur-ing the 12th week of gestation [1], this causes the forma-tion of an accessory sac from the peritoneum coveringthe umbilicus. The membrane may cover the entire orpart of the small bowel from the duodeno-jejunal junc-tion down to the ileo-colic junction [2].The two commonest clinical presentations are: acute

    small bowel obstruction or incidental diagnosis duringlaparotomy for another condition [4], however, manycases are incidental findings at autopsy. Some patientsmay have episodes of intermittent colicky abdominalpain or episodes or sub-acute small bowel obstruction,prior to a definitive diagnosis,Diagnosis of PE pre-operatively may be impossible

    because plain abdominal x-ray may be normal or onlyshow dilated small bowel loop and CT scan findings canbe very non-specific [3]. Membrane division during sur-gery is curative (assuming there is no ischaemic bowel)[2]. On literature search no re-operation was reportedon PE after dividing the encasing membrane.Knowledge of this congenital anomaly is of potential

    use to the abdominal surgeon, as its presence is notreported in standard anatomical descriptions. Its pre-sence is a source of potential confusion, particularly in

    * Correspondence: [email protected] Surgery Department, Princess of Wales Hospital, (Coity Road),Bridgend, (CF31 1PU), UK

    Al-Taan et al. Cases Journal 2010, 3:13http://www.casesjournal.com/content/3/1/13

    © 2010 Al-Taan et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative CommonsAttribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction inany medium, provided the original work is properly cited.

    mailto:[email protected]://creativecommons.org/licenses/by/2.0

  • laparoscopic surgery after establishing pneumo perito-neum. The use of laparoscopy to carry out abdominalsurgery is increasing, knowledge of this anatomicalanomaly would allow a surgeon, who recognised themembrane as PE, to divide the membrane laparoscopi-cally without recourse to conversion to openlaparotomy.

    ConsentWritten informed consent was obtained from the patientfor publication of this case report and accompanying

    images. A copy of the written consent is available forreview by the Editor-in-Chief of this journal.

    Authors’ contributionsOA prepared the manuscript. ME carried out the literature search and editedthe manuscript. JS conceived the idea to write the case report and editedthe manuscript. All authors read and approved the manuscript.

    Competing interestsThe authors declare that they have no competing interests.

    Received: 14 October 2009Accepted: 9 January 2010 Published: 9 January 2010

    Figure 1 Peritoneal encaspulation of the small bowel observed after opening the abdomen.

    Figure 2 Small bowel loops visible through the sheet of the peritoneal encapsulation.

    Al-Taan et al. Cases Journal 2010, 3:13http://www.casesjournal.com/content/3/1/13

    Page 2 of 4

  • Figure 3 Superior attachment of PE to the inferior surface of the transverse colon with greater omentum.above, inferior and lateralattachments have been divided.

    Figure 4 Membrane of peritoneal encapsulation is being held up by the operating surgeon, with the small bowel visible inferiorly.

    Al-Taan et al. Cases Journal 2010, 3:13http://www.casesjournal.com/content/3/1/13

    Page 3 of 4

  • References1. Naraynsingh V, Maharaj D, Singh M, Ramdass MJ: Peritoneal encapsulation:

    a preoperative diagnosis is possible. Postgrad Med J 2001, 77:725-726.2. Sherigar* JM, McFall B, Wali J: Peritoneal encapsulation: presenting as

    small bowel obstruction in an elderly woman. Ulster Med J 2007, 76(1):42-44.

    3. Chew MH, Sophian Hadi I, Chan G, Ong HS, Wong WK: A problemencapsulated: the rare peritoneal encapsulation syndrome. SingaporeMed J 2006, 47(9):808-10.

    4. Wirnsberger GH, Ganser K, Domej W, Sauseng G, Moore D, Moczygemba M,Krejs GJ: Sclerosing encapsulating peritonitis: differential diagnosis toperitoneal encapsulation and abdominal cocoon. Z Gastroenterol 1992,30(8):534-7.

    doi:10.1186/1757-1626-3-13Cite this article as: Al-Taan et al.: An asymptomatic case of peritonealencapsulation: case report and review of the literature. Cases Journal2010 3:13.

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    Al-Taan et al. Cases Journal 2010, 3:13http://www.casesjournal.com/content/3/1/13

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    http://www.ncbi.nlm.nih.gov/pubmed/11677284?dopt=Abstracthttp://www.ncbi.nlm.nih.gov/pubmed/11677284?dopt=Abstracthttp://www.ncbi.nlm.nih.gov/pubmed/17288307?dopt=Abstracthttp://www.ncbi.nlm.nih.gov/pubmed/17288307?dopt=Abstracthttp://www.ncbi.nlm.nih.gov/pubmed/16924364?dopt=Abstracthttp://www.ncbi.nlm.nih.gov/pubmed/16924364?dopt=Abstracthttp://www.ncbi.nlm.nih.gov/pubmed/1413936?dopt=Abstracthttp://www.ncbi.nlm.nih.gov/pubmed/1413936?dopt=Abstracthttp://www.biomedcentral.com/http://www.biomedcentral.com/info/publishing_adv.asphttp://www.biomedcentral.com/

    AbstractIntroductionCase reportDiscussionConsentAuthors' contributionsCompeting interestsReferences