“…As hepatocellular insufficiency is rarely a feature of PLD, unlike renal involvement ( 5 ), treatments for PLD are generally indicated when patients become symptomatic. Some interventional approaches, such as transcatheter arterial embolization (TAE) ( 6 , 7 ) and needle aspiration with sclerotherapy ( 8 ), have been attempted, but outcomes were insufficient. Treatment for symptoms of PLD, such as pain and digestive and/or respiratory discomfort due to hepatomegaly, thus remains largely surgical, ranging from fenestration with or without partial hepatic resection to liver transplantation (LT) ( 9 ).…”