A Glimpse Into Isolated Polycystic Liver Disease: Image Case

Abstract

Autosomal-dominant polycystic liver disease is a rare genetic disorder characterized by the formation of cysts on the liver that can progress and replace liver tissue. It leads to symptoms such as early satiety, compression of adjacent organs, and abdominal discomfort. While some patients may remain asymptomatic, others develop symptoms that significantly impact their quality of life. We present a 53-year-old man who presented with symptoms and was incidentally found to have autosomal-dominant polycystic liver disease. Treatment is limited, with surgical interventions and medical management being the mainstays. Early diagnosis and management are essential to mitigate symptoms and improve patient outcome.