GI - Liver Disease Flashcards

1
Q

A 32 year old woman returns from a holiday in India. She started getting diarrhoea after eating at a seafood restaurant on the last night. She is feverish, nauseous and is sore all over. The whites of her eyes are yellow.

Hepatitis A
Hepatitis B
Hepatitis C
Hepatitis D
Hepatitis E
A

Hepatitis A

India
Diarrhoea
Seafood restaurant
Feverish, nauseous
Sore all over
Yellow
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2
Q

Viral Hepatitis General Presentation

A

3 main signs and symptoms, apply to ALL hepatitits:

Fever
Jaundice
Raised ALT and AST

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3
Q

Hepatitis A and E

A

Faeco-oral hepatitis.

“The Vowels hit your Bowels”

Hep A:
Asymptomatic (usually)
Acute
(may be nausea and vomiting)

Hep E:
Enteric
Epidemics (water)
Expectant mothers

–> Management:
Supportive
Avoid alcohol

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4
Q

A 29 y/o male comes to the GP with fever, fatigue, joint pain and urticaria-like skin rash. He had unprotected anal sex a month ago. He comes back a week later for a blood test, which shows raised ALT and AST.
Now, he complains of feeling sick, RUQ pain and looks a bit yellow.

Hepatitis A
Hepatitis B
Hepatitis C
Hepatitis D
Hepatitis E
A

Hepatitis B

Fever
Fatigue
Joint pain
Urticaria like skin rash
Anal sex
ALT and AST
Feeling sick
RUQ pain 
Yellow
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5
Q

Hepatitis B summary

A

Initial infection - prodrome:
Flu-like symptoms (fever, myalgia, malaise)
Rash
Lymphadenopathy

--> Acute infection:
Nausea
Anorexia
RUQ pain
Jaundice

Outcome of infection:
90% Completely recover
10% Develop chronic infection

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6
Q

Hepatitis B Management

A

Acute: Symptom supportive
Chronic: Consider Peginterferon Alpha or Tonfovir

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7
Q

A 67 year old man is investigated under the two-week wait for jaundice, tender hepatomegaly, ascites and anorexia. His blood tests show a raised aFP. He mentions that he was diagnosed with hepatitis years ago. What virus(es) are likely?

Hepatitis A
Hepatitis B
Hepatitis C
Hepatitis D
Hepatitis E
A

Hep B and C

Two week wait
Jaundice
Tender hepatomegaly
Ascites
Anorexia
aFP
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8
Q

Hepatitis and Hepatocellular carcinoma

A

Hepatitis is the most common risk factor for developing HCC

Hep B:
The virus integrates into the host chromosome
Acts and an oncogene

Hep C:
Causes chronic inflammation
Mutations accumulate

Alpha-fetoprotein is marker of HCC!

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9
Q

Which hepatitis virus requires another virus to be present for it to successfully infect?

Hepatitis A
Hepatitis B
Hepatitis C
Hepatitis D
Hepatitis E
A

Hep D

Hepatitis D needs the Hepatitis B surface antigen (HBsAg) to enter hepatocytes

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10
Q

Kayser-Fleischer Rings

A

Dark rings that appear to encircle the iris of the eye. Due to copper deposition in part of the cornea.

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11
Q

Wilson’s Disease Inheritance, Pathology, Presentation

A

Inheritance: Autosomal Recessive

Pathology: Copper incorporation into caeruloplasmin in hepatocytes and its excretion into bile is impaired, and so copper is deposited, firstly into liver, then basal ganglia

Presentation: Children with liver failure or young adults with CNS signs such as ataxia, tremor, dysarthria. Kayser-Fleischer Rings are pathogomonic.

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12
Q

A 56-year-old man, diagnosed with emphysema, presents with a one-month history of jaundice and ascites. Your registrar tells you that the man has had breathing problems for the majority of his life.

What is the most likely diagnosis?

Sickle Cell Disease
COPD
Epstein-Barr Virus
Idiopathic Pulmonary Fibrosis
Alpha-1 Antitrypsin Deficiency
A

Alpha-1 Antitrypsin Deficiency

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13
Q

Alpha-1 Antitrypsin Deficiency Inheritance, Pathology, Presentation

A

Inheritance: Autosomal Recessive

Pathology: A1AT is genetically mutated, leading to it being prevented from release from hepatocytes. This causes a loss of its protective function in the lungs against elastase, leading to emphysema and a build up in the liver leading to destruction and liver disease.

Presentation: Emphysema in a non-smoker from a young age with late onset liver sign and a few risk factors

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14
Q

Liver Failure stages

A

Healthy liver

Fatty liver
deposits of fat lead to liver enlargement

Liver fibrosis
scar tissue forms

Cirrhosis
growth of connective tissue destroys liver cells

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15
Q

A 63-year-old woman stumbles into A+E. She looks unwell with a flushed face. An F1 mentions that when she presented last week, examination of her upper limbs suggested a sensory polyneuropathy.

Cytomegalovirus
Primary Biliary Cirrhosis
Paracetomal Overdose
Alcoholic Liver Disease
Primary Sclerosis Cholangitis
A

Alcoholic liver disease

Stumbles into AandE
Flushed face
Presented last week
Sensory polyneuropathy

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16
Q

A 65 year old presents with suspected liver failure. Which of the following tests would NOT be included in a liver screen for liver failure?

Alpha-1 Antitrypsin
Caeruloplasmin
HIV Screen
Anti-GBM Antibody
Aspartate Aminotransferase
A

Anti-GBM antibody

Anti-glomerular basement membrane antibody (anti-GBM Ab) is an antibody which is found in Goodpasture’s syndrome.
Goodpasture’s is a rare autoimmune disease in which antibodies attack the basement membrane in lungs and kidneys, leading to bleeding from the lungs and kidney failure.

17
Q

A 56-year-old man with a long history of alcohol abuse presents to the emergency department with abdominal pain. On examination he has a distended abdomen with shifting dullness and has a temperature of 38.2°C.

What is the most likely diagnosis?

Bowel obstruction
Liver cirrhosis
Mallory–Weiss syndrome
Perforated peptic ulcer
Spontaneous bacterial peritonitis (SBP)
A

SBP

Long history of alcohol abuse
Pain
Distended abdomen
Shifting dullness
Temp 38.2
18
Q

Signs of Chronic Liver Disease

A

A-J of liver disease

Effects of portal hypertension:
Oesophageal varices --> haematemesis + melena
Gastropathy --> melena
Splenomegaly
Dilated abdo veins (caput medusae)
Ascites
Rectal varices (hemorrhoids)
Effects of liver cell-failure:
Coma
Fetorhepaticus
Spider naevi
Gynecomastia
Jaundice
Ascites
Loss of sexual hair
Testicular atrophy
Liver flap
Bleeding tendendcy (decreased prothrombin)
Anemia - macrocytic/iron deficiency (blood loss)
Ankle oedema
19
Q

Liver disease Ix

A
Bedside: 
Obs
BM
Fluid balance
Wt
Bloods:
LFTs (pre/post; including albumin) 
INR
FBC
UandEs
CRP
Liver screen: autoantibodies, alpha-1 antitrypsin, caeruloplasmin, serum copper, ferritin, viral hepatitis serology
Imaging:
US abdomen and portal vein doppler
CXR
CT
MRI
MRCP

Special:
Ascitic tap
OGD (varices)
Liver biopsy

20
Q

Liver Disease DDx

A
(Decompensated) Alcoholic Liver disease
Viral liver disease
Autoimmuned liver disease - Wilson's, Hereditary Haemochromatosis, etc
Hepatocellular carcinoma
Pancreatic cancer
Cryptogenic liver cirrhosis
21
Q

Liver disease management

A
Conservative: 
Alcohol abstinence
Optimise nutrition
Low salt diet
Fluid restriction
Medical:
Vit. B supplementation (IV/PO), chlordiazepoxide
Diuretics
Paracentesis (give albumin)
NG feeding
Abx (? SBP)
Steroids and albumin (NB avoid NaCL)
Lactulose in hepatic encephalopathy

Surgical:
TIPSS (Transjugular intrahepatic portosystemic shunt)
Liver transplant

22
Q

A 66-year-old man presents to his GP with increasing weight loss, lethargy and fever over the last 3 months. He has also noticed pale stools and dark urine.

Crigler-Najjar Syndrome
Gilberts Syndrome
Opiate Overdose
Pancreatic Carcinoma
Haemolysis
A

Pancreatic carcinoma

Wt loss
Lethargy
Fever
3 months
Pale stools
Dark urine
23
Q

A 50-year-old man comes to you because he is worried about his skin which occasionally turns yellow. On further questioning you notice that these episodes are particularly bad during periods of stress or illness. He is otherwise well.

Gilbert’s Syndrome
Hepatic Metastases
Megaloblastic Anaemia
Hepatitis A
Dubin-Johnson Syndrome
A

Gilbert’s syndrome

Gilbert’s syndrome is a common genetic liver disorder found in 3-12% of the population.

It produces elevated levels of unconjugated bilirubin in the bloodstream (hyperbilirubinemia), but this normally has no serious consequences, although mild jaundice may appear under conditions of exertion or stress.

The cause of this hyperbilirubinaemia is the reduced activity of the enzyme glucuronyltransferase, which conjugates bilirubin and a few other lipophilic molecules.

24
Q

Jaundice

A

Dysfunctional uptake/metabolism/excretion of bilirubin
Excess bilirubin leaks into blood stream
Yellow skin and scleral icterus

3 categories:
pre-hepatic
hepatocellular
post-hepatic

25
Q

Pre-hepatic jaundice + causes

A

Dysfunctional transport from spleen–>liver
Increased unconjugated bilirubin

  1. Haemolysis (low Hb, malaria, haemolytic anaemias, RCC abnormalities - spherocytosis elliptocytosis)
  2. Inherited disorders of bilirubin metabolism (Gilbert’s - occasional jaundice, isolated high bilirubin)
26
Q

Hepatocellular Jaundice + causes

A
Dysfunctional Hepatocytes
Abnormal conjugation/excretion
Increased bilirubin (conjugated or unconjugated)
Viral - Heps A/B/C/E, EBV, CMV
Alcohol
Drugs - paracetamol, isoniazid, rifampacin
Autoimmune - PBC, PSC
Metabolic (rarer)
27
Q

Post-hepatic jaundice + causes

A
Obstructive jaundice
Increased conjugated bilirubin
Flow of bilirubin into GI tract is blocked
-->forced into renal system = dark urine
-->less stercobilin = pale stools
  1. Stones in common bile duct (RUQ pain - colicky with fatty foods)
  2. Carcinoma at head of pancreas (FLAWS)
  3. Stricture