Focal Lesions in the Liver Flashcards

1
Q

solid liver lesions

A

older patients = malignant with metastases

chronic liver disease = primary liver cancer

non cirrhotic patients = haemangioma

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2
Q

benign

A

haemangioma
focal nodular hyperplasia
adenoma
liver cysts

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3
Q

malignant

A

primary liver cancers - hepatocellular carcinoma, cholangiocarcinoma

metastases

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4
Q

haemangioma

A

female>males

commonest liver tumour
hypervascualr
usually asymptmatic

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5
Q

haemangioma - diagnosis

A

US - echogenic spot
CT - venous enhancement from periphery to centre
MRI - high intensity area
no need for FNA

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6
Q

haemangioma - treatment

A

no need for treatment

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7
Q

focal nodular hyperplasia (FNH)

A

benign nodule formation of normal liver tissue

congenital vascular anomaly - associated with Osler-weber-rendu and liver haemangioma

central scar containing a large artery, radiating branches to the periphery

hyperplastic response to abnormal arterial flow

sinusoids, bile ductules and kupffer cells present on histology

minimal pain

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8
Q

focal nodular hyperplasia (FNH) - diagnosis

A

US - nodule with varying echogenicity
CT - hyper vascular mass with central scar
MRI - iso or hypo intense
FNA - normal hepatocytes and kupffer cells with central core

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9
Q

focal nodular hyperplasia (FNH) - treatment

A

no treatment necessary

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10
Q

hepatic adenoma

A

benign neoplasm composed of normal hepatocytes no portal tract, central veins or bile ducts

female>male
associated with contraceptive hormones

RUQ pain

rupture, haemorrhage or malignant transformation

transformation risk higher in males

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11
Q

hepatic adenoma - diagnosis

A

US - filling defect
CT - diffuse arterial enhancement
MRI - hypo or hyper intense lesion
FNA - may be needed

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12
Q

hepatic adenoma - treatment

A

stop hormones, weight loss

surgical excision

imaging after 6 months

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13
Q

simple cyst

A

liquid collection lined by an epithelium
no biliary tree communication

solitary and uniloculated

asymptomatic

intracystic haemorrhage, infection, rupture, compression

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14
Q

simple cyst - management

A

no follow up necessary
doubt = image in 3-6months

surgical intervention

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15
Q

hydatid cyst

A

echinoccocus granulosus

endemic regions - Eastern Europe, central america, South America, Middle East and North Africa

disseminated disease or erosion of cyst into adjacent structures and vessels

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16
Q

hydatid cyst - diagnosis

A

detection of anti-echinoccus antibodies

17
Q

hydatid cyst - mangement

A

surgery
conservative
radical
risks

medical = albendazole

percutaneous drainage

18
Q

polycystic liver disease

A

embryonic ductal plate malformation of the intrahepatic biliary tree

numerous cysts throughout liver parenchyma

Von meyenburg complexes (VMC)

polycystic liver disease

autosomal dominant polycystic kidney disease

19
Q

Von meyenburg complexes (VMC)

A

benign cystic nodules throughout the liver

cystic bile duct malformations, originating form the peripheral biliary tree

remanants develop into small hepatic cysts and usually remain silent during life

not gremlin genetically driven

incidental finding

20
Q

polycystic liver disease

A

liver function preserved renal failure rare

symptoms = size dependent

PPKCSH and SEC63

21
Q

autosomal dominant polycystic kidney disease

A

renal failure due to polycystic kidneys and non-renal extra-hepatic features are common in ADPKD

potential massive hepatic enlargement

PKD1 and PKD2

22
Q

liver abscess

A

high fever
leukocytosis
abdominal pain
complex liver lesion

history
abdominal or biliary infection
dental procedure

23
Q

liver abscess - management

A

initial empiric broad spectrum antibiotics

aspiration/drainage percutaneously

echocardiogram

operation if no clinical improvement

4 weeks antibiotic therapy with repeat imaging

24
Q

hepatocellular carcinoma (HCC)

A

most common primary liver cancer
men>female

risk factor = cirrhosis

25
Q

hepatocellular carcinoma (HCC)

A

weight loss and RUQ pain

asymptomatic

worsening of pre-exisiting chronic liver disease
acute liver failure

signs of cirrhosis
hard enlarger RUQ mass
liver bruit

26
Q

hepatocellular carcinoma (HCC) - labs

A

AFP (alpha fetoprotein)
>100mg/ml
elevation seen in 60-80%

27
Q

hepatocellular carcinoma (HCC) - diagnosis

A
presentation
elevated AFP
US
triphasic CT scan - very early arterial perfusion 
MRI
biopsy
28
Q

hepatocellular carcinoma (HCC) - prognosis

A

tumour size

extrahepatic spread

underlying liver disease and patient performance

29
Q

hepatocellular carcinoma (HCC) - LIVER TRANSPLANTATION

A

best available treatment

removes tumour and liver

only if single tumour less than 5cm or less than 3 tumours less than 3 cm each

recurrence rate is low

30
Q

hepatocellular carcinoma (HCC) - RESECTION

A

feasible for small tumours with preserved liver function (no jaundice or portal HTN)

recurrence rate is high

31
Q

hepatocellular carcinoma (HCC) - LOCAL ABLATION

A

for non resectable

advanced liver cirrhosis

alcohol injection
radio-frequency ablation

temporary measure only

32
Q

hepatocellular carcinoma (HCC) - chemoembolization

A

TransArterialChemoEmbolization
TACE

inject chemotherapy selectively in hepatic artery

inject an embolic agent

only in patients with early cirrhosis

no role for systemic chemotherapy

33
Q

fibro-lamellar carinoma

A

presents in young patients

not related to cirrhosis

AFP is normal

CT shows typical stellate scar with radial septa showing persistent enhancement

surgical resection or transplantation is the standard of care for fibrolamellar carcinoma

TACE for patients with unresectable tumour

34
Q

secondary liver metastases

A

common site for blood born metastases

mild cholestatic picture (ALP) with preserved liver function

Dx imaging for FNA

treatmetn depends on the primary cancer

resection or chemoebolization is possible