image of the issue Available from: URL: http://www.jgld.ro/2015/2/7/html DOI: http://dx.doi.org/10.15403/jgld.2014.1121.242.hlx The Helix Sign in the Peritoneal Encapsulation Syndrome: a New Sign in a Rare Cause of Bowel Obstruction? Vasileios Mitrousias1, Evangelos Alexiou2, Apostolos Katsanas1, Konstantinos Batzalexis1, Stylianos Germanos1 1) Department of Surgery; 2) Department of Radiology, General Hospital of Larissa Koutlimbanio & Triantafylio, Larissa, Greece A 78-year-old male was referred to the emergency department with three-day history of bilious vomiting and abdominal pain and no previous abdominal surgery. The initial clinical examination revealed abdominal tenderness with mild distension without peritoneal signs. Abdominal X-ray was indicative of small bowel obstruction. No significant changes were found in the blood tests. A CT scan revealed a mild small bowel dilatation with no discrete transition point and a membranous, thin septum which seemed to surround the small intestine resembling a thickened accessory peritoneal sac (Fig.1). The 3D volume rendered images illustrated a helical-pattern mass of small bowel loops displaced anteriorly (Fig.2). An explorative laparotomy under spinal anesthesia was performed. The laparotomy revealed a thin, fibrous peritoneal sac, with the borders extending from the level of the mesocolic root superiorly, up to the level of the urinary bladder inferiorly and between the ascending and the descending colon, laterally. A small bowel loop was trapped into a small perforation of the sack causing bowel obstruction (Fig.3). The sac was partially excised. A sac encasing the small intestine is a rare condition, which may remain asymptomatic [1, 2] or manifest as a small bowel obstruction [3, 4]. Its cause is congenital, the result of the abnormal rotation of the mid gut loop to the abdominal cavity in the early stages of development [3]. There are no specific CT findings described so far [1]. Therefore, we believe that the helix sign in the appearance of the small intestine may well be suggestive of the presence of peritoneal encapsulation. This sign could raise the clinical awareness of this rare condition and could be beneficial: an early diagnosis could replace open laparotomy with laparoscopy. Corresponding author: Vasileios Mitrousias; vasileiosmitrousias@gmail.com Conflicts of interest: None to declare. References 1. Al-Taan OS, Evans MD, Shami JA. An asymptomatic case of peritoneal encapsulation: case report and review of the literature. Cases J 2010; 3: 13. doi: 10.1186/1757-1626-3-13 2. Kumara TL, Kollure SK. A case of peritoneal encapsulation syndrome. Ceylon Med J 2009; 54: 17-18. doi: 10.4038/cmj.v54i1.468 3. Naraynsingh V, Maharaj D, Singh M, Ramdass MJ. Peritoneal encapsulation: a preoperative diagnosis is possible. Postgrad Med J 2001; 77: 725-726. doi: 10.1136/pmj.77.913.725 4. Stewart D, Rampersad R, King SK. Peritoneal encapsulation as a cause for recurrent abdominal pain in a 16-year-old male. ANZ J Surg 2014. doi: 10.1111/ans.12907. J Gastrointestin Liver Dis, June 2015 Vol. 24 No 2: 144