Haemobilia is a rare cause of upper gastrointestinal bleeding that consists of haemorrhage within the biliary tree. Most cases of haemobilia are due to iatrogenic cause, laparoscopic or open cholecystectomy, abdominal trauma, gallstones, hepatic tumours, vascular aneurism. We present the case of a male patient admitted in the surgery department for epigastric and right hypochondria pain, nausea and vomiting. Open cholecystectomy was performed with a trans-cystic tube drainage. Postoperative outcome was favourable but with a continuous decrease in haemoglobin level. In the 13th day postoperatively biliary drainage was 800 ml - haemobilia. Patient health status altered and melena and hematemesis occurred. Endoscopy, cholangiography and abdominal computer tomography (CT) were performed. The episode repeated in day 27 after initial surgery. Duodenotomy and exploration of the biliary tree was performed. Angiography was performed next day that revealed biliary-arterial fistula within segment IV of the liver followed by embolization. Haemobilia reoccurred fifteen days later and colonoscopy and angiography were performed. Embolization with metallic coils was performed. Patient outcome was favourable and was discharged 13 days after second embolization. Interventional angiography remains the first treatment option of haemobilia. Selective arterial ligation or hepatectomy remain the options in case of lack of angiography or insufficient results after embolization.

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Intestinal intussusception is a frequent paediatric pathology, but adult cases are rare and do not have a specific presentation. In most cases adult intestinal intussusception, regardless of its localisation, is caused by an endoluminal tumour, which can be of multiple pathological types. We report a sigmoido-rectal intussusception in an adult in whom an adenoneuroendocrine tumour was identified as the lead point. This case is unique for the following reasons: (1) neuroendocrine tumours rarely involve the sigmoido-rectal segment of the gut, (2) clinical presentation with a recto-sigmoidal intussusception presented a diagnostic challenge.

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