wk 6 3 Focal Lesions in Liver Flashcards

1
Q

solid liver lesions in elderly more likely to be

A

malignant

with metastases more common than primary liver cancer in the absence of liver disease

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2
Q

solid liver lesions in chronic liver disease is more likely to be primary liver cancer t./f

A

true

cirrhossi/hepB

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3
Q

if non cirrhotic, what is the most commmon solid liver tumour

A

haemangioma

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4
Q

other than haemangioma, what else can be benign 3

A

focal nodular hyperplasia
adenoma
liver cysts

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5
Q

haemangioma more lkely in males than females t/f

A

false

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6
Q

how is haemangioma typically diagnosed

A

US (echogenic spot, well demarcated)
CT - venous enhancement from periphery to center
MRI - high intense area
no need for biopsy

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7
Q

treatment for haemangioma

A

none

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8
Q

name given for benign nodule formation of normal liver tissue

A

Focal Nodular Hyperplasia (FNH)

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9
Q

classical clinical feature of FNH

A

central scar contaooning a large artery, radiatin branches to periphery

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10
Q

FNH is usually symptomatic, however what may be a symtpom

A

ab pain

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11
Q

FNH diagnosed through ultrasound t.f

A

true

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12
Q

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

A

Hepatic Adenoma

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13
Q

Hepatic adenoma is associated with contraceptive pill t/f

A

true

10:1 ratio female - male

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14
Q

hepatic adenoma diagnosed by

A

US (filling defect)

Ct nd MRI used also

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15
Q

t/f biopsy required for hepatic adenoma

A

true

rule out malignancy

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16
Q

treatment for males for hepatic adenoma

A
surgical excision (higher risk of malignancy) 
q
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17
Q

treatment for woman for hepatic adenoma

A

stop hormones, weight loss
<5 - annual MRI
>5 - surgical excision

18
Q

differences between adenomaa and FNH

A

only hepatocytes, FNH contains all liver structre (bile ducts ect)
adenoma - may lead to malignancy

19
Q

5 types of cysts

A
simple 
hydatid 
atypical 
polycystic lesion 
Pyogenic/ amoebic abscess
20
Q

most common cyst

A

simple cyst

21
Q

how does a simple cyst appear

A

liquid collection lined by epithelium

22
Q

associated symptoms of simple cyst

A

intracystic haemorrhage
infection
rupture (rare)
compression

23
Q

t/f no follo up required for simple cyst

A

true unless doubt (imaging 3-6months)

sympomatic - surgical

24
Q

hydatid cyst is echinococcus granulosus, how is it diagnosed

A

history appearance

detection of anti-echinococcus antibodies

25
Q

management of hydatid cyst

A
surgery 
-open cystectomy
pericystectomy/lobectomy 
may be given albendazole
drainage
26
Q

define polycystic liver disease

A

embryonic ductal plate malformation of intrahepatic biliary tree
numerous cyts
3 typess - von meyenburg complexes, PLD, autosomal dominant poolycystic kidney disease

27
Q

t/f VMC are benign cysts

A

true

Cystic bile duct malformations, originating from the peripheral biliary tree

28
Q

PCLD more likely to cause liver failure than ADPKD

A

false

29
Q

symptoms of PCLD

A

ab pain

ab distension

30
Q

t/f for polcystic liver dieeases, invasive procedures are unlikely

A

true, only in slect with liver failure

conservative treatment to allow ab decompresion/ alleviate symptoms

31
Q

which drug is given for PLD

A

somatostatin

32
Q

clinical features of liver absces

A

high fever
leukocytosis
ab pain
complex liver lesion

likely to come from an ab/biliary infection or dental procedur

33
Q

how is liver abscess treate

A

initial empiric broad spectrum antibiotics
drainage
eechocardiogram
operation if no improvement
4 weeks antibiotic therapy with repeat imagin

34
Q

HCC is carcinoma of liver, risk factors of it 5

A
(cirrhosis from any cause) 
/hep B
hep C
alcohol 
aflatoxin
other
35
Q

clinical features of HCC

A

wt loss and RUQ pain
worsening/pre-existing chronic liver diease
acute liver failure

signs of cirrhosis
hard enlarged RUQ mass
liver bruit (rare)

36
Q

what is AFP, what does it indicate

A

Alfa fetoprotein

HCC tumour marker (>100 indicates)

37
Q

mri may be used for HCC t/f

A

true

if <1cm/ difficult to diagnose

38
Q

HCC is dependant on the Child-Purgh score, broken into stage0, stage A-C and Stage D, what is each

A

0 - very early, single tumour <2cm, resection if portal pressure is normal

A - single tumour/3nodules, <3cm, management depends on underlying liver disease
B - multinodular - transarterial chemoemolisation reqd

C - advanced, portal invasion (N1,M1)
sorafenib used

D - symptomatic treatment

39
Q

TACE

A

trans arterial chemoembolisation

inject chemo then embolic agent, only in early cirrhosis

40
Q

sorafenib is

A

multikinase inhibitor - reduces tumour growth

41
Q

fibro-lamellar carcinoma more likely in young patients t/f

A

true
TACE - unresectable
surgical resection/transplant is standard