6 - Liver Pathology Flashcards

1
Q

What are some general symptoms of liver disease?

A
  • Nausea/vomiting
  • Fatigue
  • Anorexia
  • Abdominal pain
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2
Q

What are some specific symptoms of liver disease?

A
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3
Q

What is hepatic encephalopathy?

A

Decline in brain function due to severe liver disease, liver not removing toxins so building up in the blood stream

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4
Q

What are some causes of acute liver failure?

A
  • Paracetamol OD
  • Medications like aspirin in children and tetracycline
  • Acute viral infections like EBV and CMB
  • Acute excessive alcohol intake
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5
Q

What happens to the liver in chronic injury?

A
  • Cirrhosis which develops over years and is irreversible
  • Fibrosis, hepatocyte necrosis and nodules
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6
Q

What are some causes of cirrhosis?

A
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7
Q

How does the alcoholic liver disease progress?

A

- Fatty change due to alcohol metabolism (weeks, reversible)

- Alcoholic hepatitis (years, initially reversible)

- Cirrhosis (irreversible)

Though to be due to a build up of acetaldehye

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8
Q

What are some symptoms of alcoholic liver disease?

A
  • Could be asymptomatic or general

- Fatty liver: hepatomegaly

- Hepatitis: jaundice, tender hepatomegly (RUQ pain), oedema, ascites, splenomegaly

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9
Q

What are some causes of viral hepatitis and what can they cause an increased susceptibility to?

A
  • Hep B (no cure but vaccine) or C (cure but not vaccine)
  • Lead to cirrhosis and risk of hepatocellular carcinoma
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10
Q

What is non-alcoholic fatty liver disease (NAFLD) and how can we prevent it?

A
  • Similar pathogenesis to alcoholic liver disease but stimuli is related to obesity, diabetes and metabolic syndrome
  • Non-alcoholic steatohepatitis
  • Reduce risk factors so modify lifestyle and catch early
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11
Q

What are two diseases of excess deposition that lead to cirrhosis?

A

Very rare and both affect other body systems

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12
Q

What are some autoimmune disorders that can lead to cirrhosis?

A

- Autoimmune hepatitis: affects hepatocytes, ASMA, ANA

- PBC and PSC: affect biliary ducts. PBC is AMA positive and PSC is AMA negative

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13
Q

What is Budd-Chiari syndrome?

A
  • Occlusion of one of the hepatic veins that drains the liver
  • Triad of ab pain, ascites and liver enlargement
  • Can lead to cirrhosis
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14
Q

What is the portal vein made up of?

A
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15
Q

What can cause portal hypertension?

A
  • When blood flow into the liver from the portal vein is restricted, e.g from cirrhosis
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16
Q

What are some things that can occur when you have portal hypertension?

A
  • Fibrotic liver not expansive so compresses veins and increases hydrostatic pressure in portal venous system leading to ascites and splenomegaly
  • Blood can shunt from portal system to systemic venous circulation via portosystemic anastomoses not usually used so distension of veins leading to varices
17
Q

Where are the common areas of portosystemic anastomoses that lead to varices?

A

- Lower oesophagus: mucosal varices between oesophogeal and left gastric vein can bleed torentially leading to haematemesis

- Anorectal: between superior (to portal) and middle/inferior (to internal iliac) rectal veins, typically painless as above pectinate line and rarely pleed

- Umbilical: Not as common, ligament teres reopens and can lead to caput medusa

18
Q

What is hepatorenal syndrome?

A
  • Development of AKI in the presence of cirrhosis
  • All factors in flow chart lead to decrease in renal blood flow so injury
19
Q

Label the biliary tree.

A
20
Q

What are gallstones due to?

A
  • Cholesterol and bile pigments coming out of bile solution to form a solid
  • Radiolucent so won’t show up on x-ray unlike renal calculi
21
Q

What are some risk factors for developing gall stones?

A
  • High cholesterol diet
  • Overweight
  • Age (40-50s)
  • Being a woman
  • Being pregnant due to stasis
  • Pre-exisiting liver disease
22
Q

What are some complications of gallstones and how do they present differently?

A
  • Can be asymptomatic or can cause conditions if move from gallbladder to biliary tree
  • Also acute pancreatitis
23
Q

What is biliary colic and how is it managed?

A

- Temporary obstruction of cystic duct with RUQ pain, no associated inflammation

  • Pain few hours after eating fatty meal due to CCK release
  • Analgesia or elective cholecystectomy
24
Q

What is acute cholecystitis and how is it detected and managed?

A
  • Initially similar to biliary colic, impaction of stone in cystic duct so inflammatory features
  • On ultra sound there is a thick wall of the gallbladder due to inflammation and Murphy’s sign positive
  • Conservative then cholecystectomy
25
Q

What is Murphys sign?

A
26
Q

What is acute (ascending) cholangitis and how is it managed?

A
  • If a gall stone moves into the CBD and becomes impacted, can lead to obstruction and infection

- Charcot’s triad: jaundice, fever, RUQ pain

  • IV antibiotics, fluids, relieve obstruction
27
Q

How can gallstones lead to acute pancreatitis and what is the presentation of this?

A
  • Gall stone impacts in distal biliary tree
  • Pro-enzymes become prematurely activated so autodigestion of pancreas by amylases and lipases and inflammation
  • Epigastric pain radiation to back, vomiting, Cullen’s and Grey Turner sign
28
Q

What are some causes of acute pancreatitis?

A
29
Q

How can you diagnose and manage acute pancreatitis?

A
  • CT/MRI to detect necrosis, raised lipases, history has abdominal pain
  • Fluids, manage gall stones, organ support