77. Liver Tumours Flashcards
What are the different types of tumours you might find in the liver?
Metastasis Malignant primaries (HCC, cholangiocarcinoma, hepatoblastoma) Benign tumours (haemangioma, adenoma, fibroma)
Where is the likely site of a primary in liver metastasis?
Stomach, lung, colon (men)
Breast, colon, stomach, uterus (woman)
Pancreas, leukaemia, lymphoma, carcinoid tumours (rare)
Describe the malignant primary tumours you might see in the liver?
Hepatocellular carcinoma- primary hepatocytes neoplasia, caused by Hep B
Cholangiocarcinoma-biliary tree cancer,
Angiosarcoma- blood/lymph vessel cancer
Hepatoblastoma- typically presents in kids
Gastrointestinal stroma tumour- sarcomas (soft tissue cancer)
Discuss the benign tumours you would typically see in the liver?
Cysts
Heamoangioma-dont biopsy, don’t need treatment
Adenoma- (epithelial)
Focal modular hyperplasia
Fibroma- connective tissue
Benign GIST- e.g. Leiomyoma
What symptoms and signs would make you consider a liver cancer?
Fever, malaise, anorexia, weight loss, RUQ pain
Jaundice is late except in cholangiocarcinoma
Intraperitoneal heamorrhage (tumour rupture)
Helatomgelay
Decompensated liver disease (ascites, reduced clotting)
How do investigate a suspected liver tumour?
Bloods: FBC, clotting, LFT, hepatitislmserology, a-fetoprotein
USS/CT- identify lesions, guide biopsy and staging, find primary.
MRI- distinguish malignant from benign
Liver biopsy- May achieve histological diagnosis
How do you treat liver metastasis?
Mostly palliative
Certain tumours may respond to chemo (lymphomas, germ cell tumours)
Some tumours may be able to be resected (e.g. colorectal mets)
Heamobilia is a late stage symptom of hepatocellular carcinoma. It should always be considered when Quincke’s triad is observed. What is quincke’s triad?
Right upper quadrant pain
Upper GI heamorrhage
Jaundice
What causes hepatocellular carcinoma?
Hep B, Hep C Cirrhosis NAFLD Anabolic steroids Alfatoxins (mould)
What is the treatment for HCC?
Resection fo tumours <3cm
Liver transplant
TACE
Sorafenib (kinase inhibitor)
What causes cholangiocarcinoma?
Flukes (works)
PSC
Biliary cysts
HBV,HCV
What is the prognosis and treatment for cholangiocarcinoma
As most people present late with raised ALP and, bilirubin and general fatigue not a lot can be done.
Surgery is rarely an option and typically involves major hepatectomy, extrahepatic bile duct excision and caudate lobe resection
Prognosis 5 months