Background: Low phospholipid-associated cholelithiasis (LPAC) syndrome is a very particular form of biliary lithiasis with no excess of cholesterol secretion into bile, but a decrease in phosphatidylcholine secretion, which is responsible for stones forming not only in the gallbladder, but also in the liver. LPAC syndrome may be underreported due to a lack of testing resulting from insufficient awareness among clinicians.
Aim: To describe the clinical and radiological characteristics of patients with LPAC syndrome to better identify and diagnose the disease.
Clin Res Hepatol Gastroenterol
September 2020