摘要
Autosomal dominant polycystic liver disease(ADPLD)refers to a condition characterized by the presence of numerous cholangiocytes-lined and fluid-filled cysts in the liver and the absence of polycystic kidney disease.1 Although patients with ADPLD may be asymptomatic,some patients suffer from abdominal pain,gastroesophageal reflux,and nausea,because of hepatomegaly.
基金
supported by the Medical Discipine Construction Project of Pudong Health Committee of Shanghai(No.PWYgf2021-08 to S.Y.H)
the National Natural Science Foundation of China(No.82030021 to W.F.X.,82070624 to C.H.L.,and 82000581 to J.P.L.)a
the Deep Blue Talent Project of Naval Medical University to W.P.X.
