학술논문

Low-phospholipid associated cholelithiasis (LPAC) syndrome: an unusual form in an elderly and overweight woman.
Document Type
Case Study
Source
Egyptian Liver Journal. 4/18/2023, Vol. 13 Issue 1, p1-5. 5p.
Subject
*INTRA-abdominal hypertension
*OLDER women
*GALLSTONES
*INTRAHEPATIC bile ducts
*OVERWEIGHT women
*URSODEOXYCHOLIC acid
Language
ISSN
2090-6218
Abstract
Background: Low-phospholipid associated cholelithiasis (LPAC) remains an under-diagnosed condition. It can be revealed by complications such as acute cholecystitis, acute angiocholitis and acute pancreatitis. We report a case of acute pancreatitis secondary to LPAC syndrome. Case presentation: A 58-year-old woman was hospitalized for recurrent biliary-type abdominal pain after cholecystectomies. The diagnosis of acute biliary pancreatitis revealing a low-phospholipid associated cholelithiasis syndrome was retained after explorations. An abdominal ultrasound performed by an expert radiologist allowed us to confirm the diagnosis of LPAC syndrome, showing a comet tail image along the intrahepatic bile ducts. Ursodeoxycholic acid was started without waiting for the result of the ABCB4 mutation. The outcome was spectacular with complete disappearance of the symptoms after the first week. Conclusion: Expert ultrasound remains the key examination for the confirmation of the diagnosis of a low-phospholipid associated cholelithiasis syndrome. It should be requested at the slightest warning signs such as a young age less than 40 years and recurrence of biliary symptoms after cholecystectomy. [ABSTRACT FROM AUTHOR]