Hepatobilliary + Pancreas Flashcards

1
Q

What is cholangiocarcinoma

A

Cancer of the bile ducts

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2
Q

What are the sings

A
Obstructive Jaundice - dark urine, pale stools, pruitis 
Pallapble gallbladder - non tender
Painless
Abdominal fullness or pain 
systemic symptoms - fever, malaise etc
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3
Q

what is courvosier’s law?

A

Courvoisier’s law states that in the presence of a palpably enlarged gallbladder which is non-tender and accompanied with mild painless jaundice, the cause is unlikely to be gallstones –> usually pancreatic carcinoma or colangiocarcinoma

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4
Q

Where can colangiocarcinoma occur and what one is more common

A

intrahepatic or extrahepatic ducts-

Extrahpeatic = 90%

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5
Q

what is cholangiocarcinoma associated w/

A

Chronic inflammation and cholestasis
Primary sclerosising cholagnitis
Choledochral cysts

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6
Q

What is the Rx for cholangiocacinoma

A
If intrahepatic - partial liver resection +/- protal vein embolisaion 
If distal (extrahepatic) - rescetion --> whipple's procedure (proximal pancreaticduodenectomy w/ choledocho or hepaticojejustomy) 
Repsonse to chemo is poor but can be used as adjunct
Intracavity Brachytherapy (put radioactive source in patient) can help
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7
Q

What does a whipple’s procedure remove

What is joined together?

A

Distal stomach (except in pylrous preserving surgery)
Dudodenum
Head of Pancreas
Distal common bile duct
Gallbladder
rest of pancreas and jejunum, rest of bile duct and jejonum, rest of stomach and jejunum

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8
Q

what is dumping syndrome, what are the signs

A

Rapid gastric transit post abdo surgery

N+V, abdo pain and cramping, diarrhoea, post-prandial bloating, weakness, sweating, dizziness, flushing of face

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9
Q

What increases the risk of gallbladder hypomobility

A

Pregnancy
OCP
TPN
Fasting

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10
Q

What is the most common type of gallstone, and what are the other type

A

75% are mixed –> mainly cholesterol
20% are cholesteral –> large, usually solitary, more likely in females, OCP, pregnancy, high fat diet
5% are pigment stones –> associated w/ haemolysis

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11
Q

What is admirand’s triangle w/ relation to gallstones

A

Decreased bile salts, decresased lecitin and increased cholesterol caused increased chancxe of forming a cholesterol stone

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12
Q

What are complications of gallstones in the gallbladder

A

Biliary colic
Acute cholecystitis
Chronic cholsystitis
gallblader carcinoma –> calcification causes “procelain GB”
Muocele –> neck of gallbladder blocked, can become large, may become infected
Mirizzi’s syndrome –> large stone in Gb pressed on common hepatic duct causing obstructive jaundice –> can erode through

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13
Q

what are the complications of gallstones in the CBD

what about the gut?

A
Obstructive jaundice 
Pancreatitis 
Cholangitis (cholangitis = bile duct inflammation, cholecysitits = GB inflammation) 

In the gut = gallstone illeus –> large stone erodes form GB to dudoenum through fistula (formed secondary to chronic inflammation) causing obstruction in distal ileum –> look for pneumobilia, small bowel obstruction and gallstone in RLQ [riggler’s triad]
if it gets stuck in duodenum instead of ileum = Bouveret’s syndrome

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14
Q

what is biliary colic and what are the signs

A

gallbladder spasming against a stone impacted in the neck of the gallbladder (hartman’s pouch)
Causes episodes of severe acute onset RUQ pain which is constant
Pain can radiate to scapula (back)
Attacks are precipiatated by fatty foods and last <6hr
Also get tenderness in right hypochondrium
may be associated w/ nausea and vomiting

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15
Q

what is the Ix for biliary colic

A

Urine - biloirubin, urobilogen, Hb
AXR - 10% gallstones are radiopaque
USS - look for stones, dilated ducts (>6mm) and inflammaed GB
If inflammed ducts - MRCP
If uncertain - HIDA cholescinitgraphy if liver works (GB doesn’t fill)

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16
Q

What is the Rx for biliary colic

A

Conservative - rehydrate, NBM, morphine

Surgery - urgent or elective (6-12w later) lap cholecystectomy

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17
Q

What is acute cholcystitis

A

Infeciton of the gallbladder
usuaully due to stone or sludge impaction in Hartman’s pouch causing chemical and/or bacterial inflammation
5% are acalous - no stone –> sepsis, burns, DM

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18
Q

What are the features of acute cholecystits

A

Severe RUQ pain –> continuous, radiating to right scapula and epigastrum
tachycardia and SOb
fever
vomiting
+/- jaundice
Murphy’s sign
Boas sign –> hyperaesthesia below right scapula
Might palpate phlegmon –> oedema of adherent omentum and bowel can be felt as a mass
Might get empyema –> high fever, RUQ mass, requires drainage (cholecystostomy)

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19
Q

What is Murphy’s sign, what condition does it relate to

A

place 2 fingers over GB and ask patient to breathe in –> feel pain and will catch breath
Must be negative on left
Seen in acute cholecystitis

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20
Q

What are the Ix for acute cholecystitis

A

USS - show stones, dilated ducts and inflammed GB
if see dilated ducts, need MRCP
FBC - raised WCC
U+E - show dehydration from vomiting
Amylase - rule out pancreatitis
HIDA chelscintigraphy if diagnosis unsure

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21
Q

What is the Rx for acute cholecystitis

A

Conservative - NBM, fluid resus, analgesia
Abx - usually cefuroxime and metronidazole but check local guidelines
80-90% settle over 24-48hrs
May require elective lap chole once inflammation has settled - 6-12 weeks later –> if <72h from onset, can perform in acute phase
If empyema, need percutaneous drainage - cholecstostomy

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22
Q

What are the symptoms, Ix and Rx for chronic cholecystitis

A

Vague upper GI discomfort, flatulence, dyspepsia, distension/bloating, nausea
Symptoms exacerbated by fatty foods (CCK stimulates GB)
AXR shows procelain GB (can see it on AXR)
US might show stones, fibrosis or a shrunken GB
Might need MRCP
Mx = elective cholecystectomy or ERCP if US shows dilated ducts + stones

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23
Q

what are the causes of obstructive jaundice

A
stones
Ca head of pancreas
LN @ porta hepatis (where ducts come out) - TB, Ca
Inflammatory - PBC, PSC
Drugs - OCP, sulphonyureas, fluclox
Neoplastic - cholangiocarcinoma
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24
Q

what are the clinical features of obstructive jaundice

A

Jaundice - seen @ tongue frenulum first
Dark urine
Pale stools
Itchy

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25
Q

What is the Ix for obstructive jaundice

A

Urine test - dark, increased bilirubin, decreased urobilogen
LFTs - raised ALP, slightly less raised AST, increased, increased conugated bilirubin
Vit K is decreased - raised INR
Hepatorenal syndrome - raising Creatinine (no proteinuria)
Increased WCC if cholangitis
USS - dialted ducts, stone, tumours
MRCP or ERCP - Magnetic resonance/ Endoscopic retrograde cholangiopancreatography
Can do percutaneous transhepatic cholangiography

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26
Q

What is the Rx for stones in obstructive jaundice

A

Conservative - montior LFTs, vitamins ADEK, analgesia, Colestyramine (stop bile acid reabsoprtion)
Can do ERCP w/ sphincterotomy and stone extraction if worsening LFTs, no resolution or cholangitis
Surgical = open/lap stone removal with T tube placement (need to cholangiogram 8d later to ensure stone has come out)
Might need delayed cholecstectomy to prevent recurrence

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27
Q

What is ascending cholangitis

A

Inflammation of the bile ducts caused by CBD obstrction

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28
Q

What are the signs of ascending cholangitis

A

Charcot’s triad - fever/rigors, RUQ pain and jaundice

Reynold’s pentad = above + shock + confusion

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29
Q

What is Charcot’s triad, what condition is it linked w/

A

Charcot’s triad - fever/rigors, RUQ pain and jaundice

Ascending cholangitis

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30
Q

What is Reynold’s pentad, what condition is it linked w/

A

Reynold’s pentad = Fever/rigors + RUQ pain + jaundice + shock + confusion
Ascending cholangitis

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31
Q

what are the risk factors for pancreatic carcinoma (SINED)

A
Smoking
Inflammation- chronic pancreatitis
Nutrition - high fat diet
ETOH
DM
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32
Q

what are the most common type and location of pancreatic ca

A

90% ductal adenocarcinomas

60% in head

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33
Q

what are the symptoms and signs of pancreatic Ca

A

Male >60
Painless obstructive jaundice - dark urine pale stool
might have epigastric pain –> radiates to back, relived sitting forwards
Anorexia, wt loss, malabsorption
Actue pancreatitis,
Sudden onset DM
Palpable GB
Epigastric mass
Thrombophlebitis migrant (Trousseau sign) –> phlebitis caused by thrombus in different areas
Splenomegaly, ascitites (PV thrombus)

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34
Q

what tumour marker is used for pancreatic cancer

A

Ca19-9

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35
Q

What Ix is required for pancreatic ca

A
USS/ EUS (Endoscopic USS, which is better for staging than CT/MRI)
Might need CXR, laparoscopy for mets
ERCP 
Raised Calcium 
LFTs
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36
Q

What is the Rx for pancreatic cancer

A

If fit, no mets and tumour less than 3cm, can have Whipple’s procedure or distal pancreatectomy + chemo
if not fit for surgery –> stenting of CBD, palliative bypass surgery (cholecysrtojujostomy + gastrojujostomy).
Need pain relief = might need coeliac plexus block
mean survival <6m

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37
Q

what is I GET SMASHED an acronym for

A

Acute pancreatitis

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38
Q

What are the causes of acute pancreatitis (I GET SMASHED)

A
Idiopathic 
Gallstones
Ethanol 
Trauma
Steroids
Mumps/Malignancy 
Autoimmune (e.g PAN)
Scorpion bite
Hyperlipiademia
ERCP
Drugs (thiazides, azathioprine, valproate)
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39
Q

What are the signs and symptoms of acute pancreatitis

A

Severe epigastric pain, radiating to back, relieved by sitting forwards
Vomiting
Increased HR and RR
Shock
Fever
Epigastric tenderness
Jaundice
Ileus (failure of peristalsis) = absent bowel sounds
Ecchymoses - Grey Turner (flank), Cullens (periumbilical)

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40
Q

What is the modified Glasgow criteria used for in acute pancreatitis, and what does it contain?

A
Valid for ETOh and gallstones
Used to assess severity and predict mortality 
PaO2 <8
Age >55
Neutrophils >15
Ca <2
Renal function (urea >16)
Enzymes LDH >600, AST >200
ALbumin <32
Sugar >10
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41
Q

what Ix is required for Acute pancreatitis

A
Amylase >1000 or 3x normal 
Increased lipase
Increased WCC
Decreased Ca2+ 
Increased glucose 
Increased CRP
Urine - glucose, raised conjugated bilirubin, decreased urobilogen
CXR - check for ARDS (also decreased O2)
USS
Contrast CT
42
Q

What is the management of acute pancreatitis

A

Need constant reassessment
Aggressive fluid resus - keep UO >30ml/hr, use catheter
NBM
NG tube if vomiting
Pethidine via PCA or morphine for analgesic
Penem ABx if suspcisious of infection or before ERCP
ERCP + spihincterectomy if dilated ducts due to gallstones
Might need laparotomy if infected pancreatic necrosis, pseudocyst or abscess

43
Q

what are the early systemic complications of acute pancreatitis

A
ARDS, pleural effusion 
Shock - hypovolaemic or septic
Renal failure
DIC 
Metabolic - decreased Ca, increased glucose, metabolic acidosis
44
Q

What are the late local complications of pancreatits

A
Necrosis
Infection
abscess 
Bleeding e/g from splenic artery
Thrombosis - splenic artery, gsstroduodenal artery, superior mesenteric artery - may cause bowel necrosis 
Portal vein thrombosis --> portal HTN 
Fistula formation e.g pancreato-cutaneous --> may cause skin breakdown 
pancreatic pseudocysts
45
Q

How does pancreatic pseudocysts presnet

A
Collection of pancreatic fluid surrounded by granulation tissue in lesser sac - Omental cavity 
esp in ETOH pancreatitis 
occurs 4-6w after acute pancreatits
Persisting abdominal pain
Epigastric mass
Early satiety
Persistanty raised amylase 
Us/CT to see
<6cm will spontaneously resolve
>6cm percutaneous drainage under US/CT
46
Q

What are the causes of chronic pancreatitis

A
Alcohol
Cystic fiborisis
Hereditary haemochromatosis 
Lympoplasmacytic sclerosing pancreatitis
Increased triglycerides
Obstruction by tumour
47
Q

What are the features of chronic pancreatitis

A

Epigastric pain, radiating to back, relieved by sitting forward or hot water bottle (erythema ab igne = rash caused by recurrent hot water bottle use )
Pain is exacerbated by fatty food or ETOPH
Steatorrhoea
Wieght loss
DM - polyuria, polydipsia
epigastric mass - psuedocyst

48
Q

what are the IX for chronic pancreatitis

A

increased glucose
decreased foecal elastase - decreased exocrine function
USS - look for pseduocysts
AXR/CT - calcifications

49
Q

What is the Rx for chronic pancreatitis

A

No ETOh
Reduce fat and increase carbs in diet
Analgesia - may need coeliac plexus block
Enzyme supplements - pancreatin
ADEK vitamins
DM management
Surgery if unremitting pain, wt loss or duct blockage –> Distal pancreatectomy, whiles, pancreaticojejuonostomy, endoscopic stenting

50
Q

what are the signs of an insulinoma

A

Fasting or exercising induced hypoglycaemioa
Stupor, confusion, LOC
Increased insulin, increased C pepitde

51
Q

What are the signs of a glucagonoma

A

Mild DM
Necrolytic migratory erythema –> red, blistering rash that spreads across the skin. It particularly affects the skin around the mouth and distal extremities

52
Q

What are the signs of a gastronoma, where are they found, what is the treatment
(Zollinger-Ellison syndrome)

A

Often found in small intestine or pancreas
Secrete gastrin
Ulcers - duodenum, stomach, SI –> refractory
chronic diarrhoea (inactivation of pancreatic enzymes) & steatorrhoea
hypergastraenima (high gastrin)
Abdo pain and dyspepsia
Rx = high dose PPI, ± tumour resection or Roux en Y

53
Q

VIPoma / WDHA syndrome signs

A

Watery diarrhoea
Hypokalaemia
Achloyhdria - absence of HCl in stomach secretions
Acidosis

54
Q

stomatostatinoma signs

A

DM –> inhibits insulin release
Steatorrhoea –> inhibits pancreastic enzyme release
Gall stones
(also inhibits glucagon release)

55
Q

what are the signs of hereditary haemochromatosis

A

May be asymptomatic
Non specific symptoms
Large/small joint pains - most commonly 2nd or 3rd MCP
Slate grey skin - increased melanin deposition
Symptoms of liver disease (hepatosplenomegaly), DM, cardiac failure (& arrhythmia)
Hypogonadism - testicle atrophy, loss of hair, gynaecomastia

56
Q

What are the Ix for Hereditary haemochromatosis

A

Increased Iron, decreased TIBC, increased ferritin and transferrin saturation (increased intestinal iron absorption is the pathogenesis of HH)
Gene testing - HFE gene mutation on Chr 6p
Liver - LFTs, biopsy, visualise iron with Perls stain, MRI
Pancreas - FBG/RBG
Heart - ECG, echo
Pituitary function tests - decreased testosterone, decreased or inappropriately normal LH, FSH (2º hypogonadism)
Joint X-ray - linear calcifications

57
Q

What is the Rx for hereditary haemochromatosis

A

if no symptoms/evidence of end organ disease - annual review
If end organ disease = weekly/twice weekly phlebotomy (1 unit - 450ml) until ferritin <50ng/ml, then every 2-4 months to maintain
If can’t tolerate phleb - chelation
Limit ETOH intake; avoid iron, vit C supplements and uncooked seafood

58
Q

what is primary biliary cirrhosis associated w/

A
Sjogren's syndrome 
Arthritis (e.g RA)
Reynaud's phenomenom - Sjogren's, CREST/ scleroderma SLE
autoimmune thyroid disease 
more common in women (9:1)
59
Q

What is primary biliary cirrhosis

A

Chronic inflammatory liver disease involving destruction of intrahepatic bile ducts, causing cholestasis and eventually cirrhosis

60
Q

What are the signs of PBC

A

initially may be asymptomatic - can be incidental finding on blood test w/ raised All phos and cholesterol
Pruruits & skin excoriations
Jaundice
hepatomegaly
Liver decompensation = ascieites, variceal haemorrhage
Signs of chronic liver disease - palmar erythema, clubbing, spider naive
fatigue, wt loss
xanthomas (yellow nodule on skin) 2º to hypercholesteraiema
signs of related conditions e.g dry eyes and mouth

61
Q

What Ix are needed for PBC

A

LFTs - Raised Alkphos, raised GGT, bilirubin &AST/ALT may rise in later stages, prolongation of PT,
Antimitochondrial antibodies, raised IgM and raised cholesterol are typical
USS - exclude extra hepatic biliary obstruction
Liver biopsy - inflammatory cells and granulomas around intrahepatic bile ducts, w/ destruction and fibrosis
Ca, phosphate and Vit D - can develop metabolic bone disease

62
Q

What are the Rx for PBC

A

Ursodeoxycholic acid = bile acid, reduces toxicity and increase elimination of retained bile acids
Pred/azathioprine/mycophenolate -if inflammatory component (overlap w/ AI hepatitis)
Pruritis - colestryarmine (binds bile acids in GI tract), rifampicin (unregulated liver enzyme which metabolise things causing pruritus), naltrexone
Bones - Ca, Vit D, bisphosphonates
Replace Vit ADEK
Portal HTN - β blockers, endoscopic banding of varicose, trans jugular intrahepatic portasystemic shunt (hepatic –> portal vein to decompress portal vein)
Liver transplant

63
Q

What is primary sclerosis cholangitis

A

Chronic cholestatic liver disease caused by progressive fibrosis and obliteration in both intrahepatic and extra hepatic ducts

64
Q

What is PSC associated w/

A

IBD, esp UC

65
Q

what are the features of PSC

A

May be asymptomatic and diagnosed after persistently raised AlkPhos
May present w/ intermittent jaundice, pruritus, RUQ pain (n/b don’t really get with PBC , wt loss, fever
Ask about cholitis
May have hepatospelnomegalt, spider naive, palmar erythema, ascites
Can get recurrent cholangitis -fever, rigors
Can also get cholangicarcinoma, and metabolic liver disease

66
Q

What are the Ix for PSC

A

Blood - raised Al;k phos, raised GGT, mild raised transaminases, later decreased albumin and increased bilirubin
Serology - raised IgM , Anti smooth muscle and ANA present in 30%, pANCA in 70% ]
ERCP - stricturing and dilation of intrahepatic duct (and occasionally extra hepatic duct) - looks like beads
MRCP - same as ERCP
Liver biopsy - stages disease

67
Q

What is the Rx for PSC

A

IF cholangitis - fluid resus, ABx (cephlasporin + metronidazole)
CHolesytrymine or phototherapy for pruritus
Vit AEDK, Calcium intake
Endoscopic/percutaenous transhepatic stenting or dilatation of major extra hepatic bile duct strictures
Liver transplant for end stage disease

68
Q

What is Wilson’s disease

A

AR disease where there is decreased biliary excretion of copper, leading to accumulation in liver and brain, due to gene mutation of copper transporting ATPASE on Chr13

69
Q

What are the signs of Wilsons disease

A

Liver - hepatitis, liver failure, cirrhosis –> easy bruising, variceal bleeding, encephalopathy, hepatosplenomegaly, jaundice, ascites, gynaecomastia
Neurological - dyskinesia, rigidity, tremor, dystonia, dysarthria, dysphagia, drooling, dementia, ataxia
Psychiatric - conduct disorder, personality change, psychosis
Eyes - green or brown Kayser flesher rings, sunflower cataract (copper accumulation in lens on slit lamp)
Copper can also damage renal tubules causing hypercalcuria, phosphaturia and renal tubular acidosis

70
Q

what are the Ix for Wilson’s disease

A

Raised AST, ALT and all phos
Serum caeruloplasmin - low
Copper (inc 24hr urinary copper) - high
Liver biopsy - increased coppper

71
Q

What is the Rx for Wilson’s disease

A
Manage in specialist unit
Copper chelators (e.g d-penicillaimine)
Oral zinc - stops absorption 
Liver and neuro care
Liver transplant may be necessary
72
Q

what is a tumour marker for HCC

A

Alpha fetoproptein

73
Q

what is a tumour marker for colorectal cancer

A

CEA

74
Q

what the fuck is Budd-chiari syndrome

A

hepatic vein thrombosis

The features are classically a triad of:
abdominal pain: sudden onset, severe
ascites
tender hepatomegaly

Causes
polycythaemia rubra vera
thrombophilia: activated protein C resistance, antithrombin III deficiency, protein C &amp; S deficiencies
pregnancy
oral contraceptive pill
75
Q

Alcoholic hepatitis Hx + Ex

A

May be asymptomatic
May be mild - nausea, malaise, RUQ pain
May be severe - jaundice, abode swelling, swollen ankles, GI bleeding
Signs of ETOH excess - malnourished, palmar erythema, duprytrens contracture, facial telangiectasia, parotid enlargement, spider naeviae, gynaecomastia, testicular atrophy, hepatomegaly, easy bruising
Signs of severe alcoholic hepatitis - febrile, tachy, jaundice, bruising, encephalopathy (liver flap, drowsiness, can’t copy 5 pointed star), fetorhepatiticus, ascites

76
Q

What is a significant marker of poor liver function

A

Prolonged PT

77
Q

What do you see on biopsy of alcoholic hepatitis

A
Centrilobular ballooning
degeneration and necrosis of hepatocytes
Steatosis
Neutrophillic inflammation
Cholestasis
78
Q

What is the Rx for alcoholic liver disease

A

Thiamine, Vit C and others (Pabrinex)
Correct K, MG, glucose
Treat encephalopathy w/ oral lactulose and phosphate enemas
Manage ascites w/ spironolactone ± frusemide
Nitrition support (protein restriction if encephalophic)
Steroids

79
Q

what is Wernicke’s encephalopathy

A

acute neurological condition characterized by a triad of ophthalmoparesis/opthalmoplegia with nystagmus, ataxia, and confusion + disorientation and disturbed memory
caused by thiamine deficiency
Reversible w/ treatment

80
Q

What is Korsakoff’s psychosis

A

Permanent impairment of retrograde and anterograde memory w/ confabulation
Caused by untreated thiamine deficiency

81
Q

What is liver failure

A

severe liver dysfunction w/ jaundice, encephalopathy and coagulopathy
Jaundice - deficient uptake, conjugation and secretion of bilirubin by liver
Encephalopathy - decreased extraction of nitrogenous products by liver –> delivered to brain
Coagulopathy –> decreased synth of clotting factors + decreased platelets (due to hypersplenism or abnormal function)

82
Q

What are the time frames for hyper acute, acute, subacute and chronic liver failure

A

Hyper acute <7d
Actue 1-4w
Subacute 4-12w
Acute on chronic = decompensation in patients w/ chronic liver disease

83
Q

What causes liver failure

A
Viral - hepatitis 
Drugs e.g paracetamol  --> paracetamol level, n-acetylcysteine
Autoimmune
Budd chiari 
hameochromatosis 
Wilson's
84
Q

what are the symptoms of liver failure

A

Jaundice
Encephalopathy
liver asteroids
fetor hepaticus
brusing/ bleeding
cities and splenomegaly less common in acute or hyper acute
can get hepatorenal syndrome, cerebral oedema, hypoglycaemia

85
Q

What is the Rx for liver failure

A

Resus
Treat cause
Monitor vital signs, PT etc
Lactulose and phosphate enema for encephalopathy
Vit K, FFP or platelet infusions for coagulopathy
PPI for gastric mucosa protection
Avoid drugs metabolised by liver
If cerebral oedema - nurse at 30º, hyperventilate, IV manitol

86
Q

what is spontaneous bacterial peritonitis

A

Spontaneous bacterial peritonitis (SBP) is infection of ascitic fluid without an apparent source
Neutrophis >250 in an ascitic tap
Rx = cefuroxime + metranidazole
Prophylaxis = ciprofloxacin

87
Q

What are the indications for liver transplant

A

If paracetamol OD - arterial pH <7/3 or Pt>100&creatinine>300&severe encephalopathy

For others (need 3 out of 5)

  • age <10 or >40
  • bilirubin >300
  • Caused by Non A, non E viral hepatitis or drugs
  • Interval from jaundice onset to encephalopathy >7d
  • Pt >100
88
Q

What is cirrhosis

A

End stage of chronic liver disease

replacement of normal liver architecture w/ diffuse fibrosis and nodules of regeneration

89
Q

What are the causes of cirrhosis

A
Chronic alcohol misuse 
Chronic viral hepatitis - B, C
Autoimmune hepaititis 
Drugs - methotrexate, hepatotoxic drugs
Inheritied - α1 antitrypsin deficiency, haemochromatosis, wilson's disease, CF
Vascular - Budd chiari
PBC
PSC
NASH
90
Q

What causes decompensation off cirrhosis

A
Infection
Gi bleeding 
constipation
high protein meal
electrolyte imabalance 
alcohol
drugs
tumour development 
portal vein thrombosis
91
Q

What are the signs and symptoms of cirrhosis

A
Early non-specific symptoms --> anorexia, nausea, fatigue, wt loss
Symptoms caused by decreased synthetic function - easy bruising, abdomen swelling, ankle oedema
Symptoms caused by reduced detoxification - jaundice, personality change, altered sleep pattern, amenorrhoea
Symptoms caused by portal HTN - abdomen swelling, haematemesis, PR bleeding, malaena, splenomegaly
Asterixis (liver flap)
Bruises
Clubbing
Duprtrynes contract
Palmar erythema 
Jaundice
leuconychia
Gynaecomastia
Scratch marks
Ascities
Liver can be large or small
Caput medusa
testicular atrophy
92
Q

What Ix is needed for cirrhosis

A
FBC - reduced Hb and platelets (due to hypersplenism) 
Decreased albumn
Prolonged PT
Serum AFP raised (can point to HCC) 
Determine cause (e.g antimitochondrial ABs for PBC, SMA for autoimmune hepatitis,)
Ascitic tap
Liver biopsy 
Imaging
93
Q

What is the child-Pugh score used for and what does it contain

A

Cirrhosis - 5-6 is grade A, 7-9 is B, 10-15 is C
Albumin >35, 28-35, <28
Bilirubin - <2, 2-3, >3
PT - <4, 4-6, >6
Ascities - None, mild mod
Encephalopathy - none, grade 1-2, grade 3-4

94
Q

Rx for cirrhosis

A

Treat cause
Avoid alcohol, sedative, opiates, NSAIDs
Encephalopathy - lactulose, phosphate enema
Ascites - Spironolactone ± furosomide, sodium restriction, therapeutic paracentesis w/ albumin replacement
SBP - ABx –> cefuorxime and metronidazole
Surgical - consider insertion of Transjugular intrahepatic portosystemic shunt to reduce portal HT
Transplant

95
Q

What antibodies are linked w/ autoimmune hepatitis

What might you see with regards to Abs on Ix of autoimmune hepatitis

A
Anti-smorh muscle 
ANA
Anti-actin antibodies (AAA)
Anti-soluble liver antigen (antiSLA)
Anti Liver/kidney microsomes (ALKM1)  - more young women 

They normally have a polyclonal hypergammaglobulinaemia

96
Q

What are the symptoms of autoimmune hepatitis

A

Classic liver stuff + systemic features
Some get amenorrhoea
Might get serum sickness - arthralgia, polyarthritis, maculopapular rash
ask about other autoimmune disease
can get cushinoid features before admin of steroids

97
Q

When do you treat autoimmune hepatitis, and what is the treatment

A

Aminotransferase >10x normal, symptomatic, or hepatitis/necrosis on histology

Induce immunesupression w/ steroids, then gradually reduce dose for maintinece
Can add azathioprine/mercaptopurine as steroid sparing maintainence
Monitor USS and αfetoprotein every 6-12m in patients w/ evidence of cirrhosis to detect HCC
Repeat liver biopsies for evidence of disease progression every ~2y
Hep A and B vaccines
Liver transplant

98
Q

what are the difference in signs between hepatitis A, B and C

A

Hep A = 3-6w after infection, following prodrome of malaise, anorexia, distaste for cigarettes, nausea; get jaundice lasting 3w
Hep B = Incubation period 3-6m, then 1-2w prodrome w/ RUQ pain and diarrhoea, then get jaundiced lasting 4-8w (but can end up w/ chronic carriage)
Hep C =mostly asymptomatic, 10% get jaundiced, but lasts chronically causing end stage liver disease, can cause GN and skin rash (caused by mixed cryoglobilinaemia causing a small vessel vasculitis)

99
Q

what can you treat chronic hep B with

A

Peginterferon or tonofovir

100
Q

how can you treat Hep C

A

elbasvir/grazoprevir, pegylated interferon α, ribavarin
If HCV 1 or 4 - treat for 24-48w
If HCV 2 or 3 treat for 12-24w

101
Q

what is the most common cause of liver abscess, what is the signs

A

Amoebic (entamoebea histolytica) is most common worldwide
otherwise can be pygoenic e.g E. coli
Fever (continuous or spiking)
Jaundice
Tender hepatomegaly - right lobe more affected
RUQ or epigastric pain, can refer to shoulder if diaphragm irritated
Can cause reactive pleural effusion
Needle aspirate/catheter drain if pyogenic + cef + met
Metronidazole and diloxanide furoate if amoebic