Lemmel's syndrome is an uncommon pathology first described in 1934,1 and is defined as an obstructive jaundice caused by a periampullary duodenal diverticulum compressing the intra-pancreatic part of the common bile duct resulting in upstream dilatation of the extra- and intra-hepatic bile ducts.2
A 74-year-old woman presented to the emergency department without any significant past medical history. The patient was being studied by the surgery department after having suffered several episodes of abdominal pain in the right hypocondrium, fever and jaundice. In addition, alkaline phosphatase, serum aspartate aminotransferase (AST), alanine transaminase (ALT), and bilirubin metabolites were all elevated.
Ultrasound revealed intra- and extra-hepatic biliary ductal dilatation, without apparent cause. The patient underwent an magnetic resonance cholangiopancreatography (MRCP) which proved dilatation of the biliary tract as well as a large duodenal diverticulum with an air-fluid level in its interior that was displacing and compressing the main biliary tract (Fig. 1), with no images suggesting cholelithiasis or choledocholithiasis; this finding was consistent with a subsequent CT study (Fig. 2). Other causes of obstruction of the bile duct were not recognized. These findings were compatible with lemmel syndrome.
The authors declare that they have no competing interest.