7.02 - HPB Liver Flashcards
What are simple liver cysts?
Fluid filled epithelial lined sacs within the liver, most commonly occurring in the right lobe.
They are thought to be due to a congenitally malformed bile duct, failing to connect to the extrahepatic ducts, leading to local dilatation filled with bile-like fluid.
What are the clinical features of simple liver cysts?
Usually asymptomatic and detected incidentally on imaging.
Around 10% of patients are symptomatic:
- abdominal pain
- nausea
- early satiety
How are liver cysts investigated?
LFTs (usually normal, although GGT may be raised)
Tumour markers CEA and CA19-9 can be elevated
Ultrasound is imaging modality of choice, showing well-defined lesions.
How are simple liver cysts managed?
Most do not require intervention.
If >4cm in side, follow-up ultrasound is recommended.
If patient is symptomatic, can do ultrasound-guided aspiration or laparoscopic de-roofing
What is polycystic liver disease?
The presence of ≥20 cysts within the liver parenchyma, caused by one of the two following autosomal dominant conditions:
- autosomal dominant polycystic kidney disease (ADPKD)
- autosomal dominant polycystic liver disease (ADPLD)
Polycystic structures are not connected to intrahepatic bile ducts and so do not drain, leading to dilatation.
What are the clinical features of polycystic liver disease?
Majority of patients are asymptomatic, however symptoms can occur due to localised compression.
Common symptoms include abdominal pain, hepatomegaly, and urinary tract symptoms.
Significant disease can eventually cause liver cirrhosis and portal hypertension.
How is polycystic liver disease investigated?
LFTs (normal, though ALP may be raised)
U&Es to examine renal function (ADPLD)
Definitive diagnosis via ultrasound imaging, demonstrating multiple cysts.
How is polycystic liver disease managed?
Asymptomatic disease left alone.
US-guided aspiration or laparoscopic de-roofing of cysts if:
- intractable symptoms
- inability to rule out malignancy
- prevention of malignancy
What are cystic neoplasms?
Make up around 5% of liver cysts, most commonly cystadenomas.
They are premalignant developing as a result of abdominal proliferation of biliary epithelium.
What are the clinical features of cystic neoplasms?
Most commonly asymptomatic
Abdominal pain, anorexia, nausea, fullness and bloating if symptomatic due to compression of local structures.
How are cystic neoplasms investigated?
LFTs normal
ALP, CEA and CA19-9 elevated
CT with contract performed
How are cystic neoplasms managed?
Liver lobe resection, with samples sent for subsequent biopsy.
What are hydatid cysts?
Tapeform Echinococcus granulosus passes via the hepatic portal system into the liver, where they continue to grow and form cysts.
What are the clinical features of hydatid cysts?
Cysts grow very slowly so can remain asymptomatic for many years.
Common presenting symptom is vague abdominal pain, caused by mass effect on surrounding structures or due to rupture.
OE jaundice or cholangitis, vomiting, dyspepsia, early satiety.
How are hydatid cysts investigated?
LFTs normal (unless cholangitis)
FBC shows eosinophilia
Ultrasound scan first line, with further imaging via CT imaging with contract