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Flashcards

MDPL 1 - Liver Structure, Function, and Dysfunction

Erica Lai English 88 cards

Cards in this deck (88)

  1. 1Location of liver (3 abdominal areas)Right hypochondrium
    Epigastric
    Left hypochondrium
  2. 22 surfaces of liver (which sides of the liver are they, shape of surface, what other organs are they in contact with)Diaphragmatic
    (anterosuperior surfaces, smooth + convex, contact with diaphragm)
    Visceral
    (posteroinferior surfaces, irregular + flat, contact with right kidney, right adrenal gland, right colic flexure, transverse colon, duodenum (1st part), gallbladder, oesophagus, and stomach)
  3. 34 lobes of liverRight
    Left
    Caudate
    Quadrate
  4. 45 ligaments of liverfalciform
    coronary
    left triangular
    right triangular
    lesser omentum
  5. 5What does the falciform ligament do (2)anatomical division of R&L lobes
    attaches anterior liver surface to the anterior abdominal wall
  6. 6What does the coronary ligament doattaches superior surface of the liver to the inferior surface of the diaphragm
  7. 7What does the lesser omentum doattaches liver to the lesser curvature of the stomach and the first part of the duodenum
  8. 8Which 2 ligaments is the lesser omentum made up ofhepatoduodenal ligament
    hepatogastric ligament
  9. 93 recesses of liverSubphrenic spaces
    Subhepatic space
    Morison’s pouch
  10. 10Clinical relevance of recesses of liverInfection may collect + form an abscess
  11. 11What kind of cell makes up the liver and its regeneration patternhepatocytes
    stable cells
  12. 12What is a liver lobulestructural unit of the liver
  13. 13what shape is a lobulehexagonal
  14. 14What drains a lobulecentral vein
  15. 15Size + weight of liver (men + women)1.5kg
    men - 10.5cm
    women - 7cm
  16. 16Where are the portal tracts and what are they made up ofperiphery of the lobule
    - arteriole
    - venule
    - bile duct
    - lymphatic vessels
    - vagus nerve
  17. 17What is the portal triadarteriole, venule + bile duct
  18. 18What are the portal tracts a branch ofarteriole - hepatic artery
    venule - hepatic portal vein
    bile duct - bile duct
  19. 19How do you identify portal tract on a histological slideportal tract connective tissue stains blue with trichromic stain
  20. 20What is a sinusoidlocation for mixing of the oxygen-rich blood from the hepatic artery and the nutrient-rich blood from the portal vein
  21. 21Where do sinusoids drain intocentral hepatic vein branch
  22. 22Blood supply of the liverdual blood supply:
    - hepatic artery
    - hepatic portal vein
  23. 23What does the hepatic artery supply (what does it bring + where does it go)oxygenated blood to non-parenchymal structures of liver
  24. 24What does the hepatic portal vein supply (what does it bring + where does it go)partially deoxygenated blood + nutrients absorbed from the small intestine to liver parenchyma
  25. 25What is the hepatic artery a branch ofcoeliac trunk
  26. 26Venous drainage pathway of livercentral vein -> hepatic vein -> IVC
  27. 27What are sinusoids lined with (2)fenestrated endothelium
    macrophages (Kupffer cells)
  28. 28Where is the space of disse + what does it containbetween sinusoids and hepatocytes
    hepatic stellate cells
  29. 29What innervates the liver parenchymasympathetic (coeliac plexus) + parasympathetic (vagus nerve fibres)
  30. 30How do nerves innervating the liver entervia porta hepatis
  31. 31What is Glisson's capsule (+ what is it's clinical function)fibrous covering of the liver innervated by branches of the lower intercostal nerves
    (distension of the capsule results in sharp, well-localised pain)
  32. 32Flow path of bile from hepatocyte -> CBDhepatocyte -> canaliculi (merge) -> ductules -> ducts -> R + L hepatic ducts -> common hepatic duct (merge w/ cystic duct) -> CBD
  33. 33What is the ampulla of Vater + where does it drainCBD + pancreatic duct
    drains into duodenum
  34. 34What is the gallbladder + its rolestorage pouch for bile
    concentrates bile
  35. 35What is the acinusfunctional unit of the liver
  36. 36Describe an acinus (shape + position)irregular shaped, roughly ellipsoidal mass of hepatocytes aligned around the hepatic arterioles and portal venules just as they join into sinusoids
  37. 37What are acini divided intozones (1 - 3)
  38. 38What is the difference between zones 1 -3 in acinuszone 1 = closest = best oxygenated
    zone 3 = furthest = poorly oxygenated
  39. 39What do the cells in zone 1 of acinus do (+ what is the impact of this)first to sense + potentially absorb blood-borne toxins absorbed into portal blood from the small intestine
    (ischaemic/toxic injury most severe in zone 3 - reflects pattern of dmg/fibrosis)
  40. 404 main functions of liverprocesses blood + breaks down/balances/creates nutrients
    metabolises drugs to make easier for rest of the body to use or make it nontoxic
    regulates most serum chemical levels
    secretes bile
  41. 41What does the liver synthesise (2)plasma proteins
    bile
  42. 42Which plasma proteins are produced by liverAlbumin
    Acute-phase proteins (e.g. CRP)
    Clotting factors (not FVIII)
    Complement proteins
    Protease inhibitors (e.g. A1AT)
    Transport proteins
  43. 43Hallmark appearance of liver with chronic venous congestionnutmeg liver
  44. 44What is chronic venous congestion caused byright heart failure - congestive heart failure or right heart failure in cor pulmonale or mitral stenosis
  45. 45LFTs in chronic venous congestionmild elevation of ALT, AST
  46. 46What is Budd Chiari syndromeObstruction to venous outflow from liver (hepatic vein/IVC)
  47. 47What is Budd Chiari syndrome associated with (4)Myeloproliferative disorder
    Inherited hypercoagulable/thrombophilic states
    OCP (rarely)
    Hepatoma
  48. 48DDx of Budd Chiari syndrome (3)acute liver failure
    acute hepatitis
    chronic liver disease
  49. 49Potential progression of Budd Chiari syndromerapid onset portal HTN/ascites
  50. 50Why are liver infarctions rare (but if it happens, why is usually the case)liver is protected via a dual blood supply
    (trauma to hepatic artery likely)
  51. 51What is ischaemic injury to the liver usually associated withacute circulatory failure
    (i.e. shock/hypotension)
  52. 52Where in the liver is most affected by ischaemic injuryzone 3 of acini
  53. 53What kind of liver is more susceptible to ishaemic injuryliver with chronic passive venous congestion or cirrhosis/portal hypertension
  54. 54What affects possible outcomes of acute liver damage (2)degree of damage?
    is damage transient or persistent?
  55. 55If damage is persistent, what does acute liver damage progress to? (+ what can this progress to)fibrosis (mild to advanced)
    may lead to cirrhosis
  56. 56Pathogenesis of liver cirrhosisconnective tissue framework damaged by continued/repeated insult = complete recovery no longer possible = fibrosis by activated hepatic stellate cells
  57. 57Main causes of liver damage (8)Alcohol
    NAFLD
    Virus
    Drugs
    Autoimmune
    Inherited metabolic disorders
    Chronic biliary disease
    Trauma
  58. 58Which heps. are acute dmg and which are chronic dmgA + E = acute
    B + C = chronic
  59. 59Eg of inherited metabolic diseases that can cause liver damage (3)HFE
    Wilson's diease
    A1AT deficiency
  60. 60Why does chronic biliary disease damage the liverautoimmune damage to bile ducts = cholestasis with injury to the liver from retained bile salts
  61. 61Where do you obtain liver cells for autopsy when classifying grade (2)portal
    periportal
  62. 62What is piecemeal necrosis (+ when is it usually seen)pattern of chronic injury occurring when portal tract inflammation spills over the interface to damage adjacent hepatocytes
    (chronic Hep B or autoimmune hepatitis)
  63. 63When is high lymphocyte from liver biopsy commonhepatitis
  64. 64What are granulomas of portal tract characteristic ofprimary biliary cirrhosis
  65. 65When do you see high neutrophils in liver Bxsuggest alcohol-related disease or NAFLD
  66. 66Stage 1 of liver fibrosisportal fibrosis - affecting all or most portal tracts
  67. 67Stage 2 of liver fibrosisperiportal fibrosis
  68. 68Stage 3 of liver fibrosisbridging fibrosis - either portal-to-portal or portal-to-central
  69. 69Stage 4 of liver fibrosisfibrous septa/bands separating regenerative nodules of liver parenchyma
    (may be enough to diagnose as cirrhosis)
  70. 70What is liver cirrhosisend-stage liver damage characterised by disruption of normal hepatic parenchyma by bands of fibrosis + regenerative nodules of hepatocytes
  71. 714 features of liver cirrhosisdiffuse distortion of liver architecture
    surrounding fibrous bands/septa
    regenerative nodules
    distorted vascular relationships
  72. 72What are vascular changes in the liver due to cirrhosis (4)destruction/thrombosis of liver veins
    collateral channels/shunts form in liver
    ‘capillarised’ sinusoids (loose fenestrations)
    raised hepatic venous pressure gradient (HVPG)
  73. 73Symptoms of cirrhosis (10)fatigue
    easy bleeding/bruising (ecchymosis)
    loss of appetite
    nausea
    peripheral oedema
    weight loss
    itchy skin (pruritus)
    jaundice
    ascites
    erythema
  74. 74What do you do to Dx cirrhosis (2)lab tests
    imaging
  75. 75What do you look in lab tests for cirrhosisbilirubin
    enzyme studies
    kidney function tests
    lood creatinine
  76. 76What imaging techniques do you use to Dx cirrhosisMRE (magnetic resonance elastography)
    (checks for hardening/stiffening of liver)
    MRI
    CT
    Ultrasound (fibroscan?)
  77. 77What is the use for Bx in cirrhosisfind severity, extent + cause of damage
  78. 78Who is screened for advanced fibrosis (NICE guidelines 2016) (3)HCV
    High alcohol intake (>50u/wk M, >35u/wk F)
    NAFLD with +ELF blood test
  79. 79How is advanced fibrosis screenedFibroscan (transient elastography)
  80. 80Active management for patient with cirrhosis (6)specific Tx/risk modification or underlying disease
    avoid further/additional insults to liver
    screen for varices
    screen for HCC
    prevent/slow/reverse progression of liver disease/development of decompensation
    listing for transplantation
  81. 81Considerations of medical interventions with someone with cirrhosis (2)adjust dose or avoid certain medications
    risks with surgery: infection, bleeding, healing, ascites
  82. 82Why are there no altered bleeding tendencies in someone with cirrhosis despite abnormal INRliver synthesis of both coagulation and anti-thrombotic proteins both affected
    (so balance remains)
  83. 83What is compensated cirrhosisasymptomatic
    may or may not have:
    - biochemical/radiological abnormalities
    - signs of chronic liver disease/portal HTN
    - varices on OGD (gastroduodenoscopy)
  84. 84how does compensated cirrhosis develop into decompensated cirrhosis (+ egs.)Further injury:
    - infection
    - bleeding
    - hypotension
    - alcohol
    - medications
    - dehydration
    - trauma
    - surgery
  85. 85Key complications of decompensated cirrhosis (7)ascites
    hepatic encephalopathy
    variceal haemorrhage
    hepatorenal syndrome (HRS)
    jaundice
    infection (esp. spontaneous bacterial peritonitis)
    hepatocellular carcinoma (HCC)
  86. 86Pathophysiology of Portal HTNincreased hepatic resistance to portal blood flow = HPVG rise
    increased by splanchnic vasodilation (NO)
    = lower TPR + BP
    = complementary increase in CO
    = hyperdynamic circulation in cirrhosis
  87. 87Methods of compensating for widespread vasodilation (4)Activation of the RAAS
    ADH secretion
    Sodium + water retention
    Reflex renal vasoconstriction
  88. 88How does ascites arise from portal HTN due to cirrhosisleakage from peritoneal vessels due to:
    - higher mean hydrostatic pressure
    - Lower oncotic pressure due to low albumin

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Flashcards on MDPL 1 - Liver Structure, Function, and Dysfunction, created by Erica Lai on 28/09/2019.
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