Cirrhosis pathophysiology

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Aditya Govindavarjhulla, M.B.B.S. [2]

Overview

Cirrhosis occurs due to long term liver injury which causes an imbalance between matrix production and degradation. Early disruption of the normal hepatic matrix results in its replacement by scar tissue, which in turn has deleterious effects on cell function.

Pathophysiology

• The liver plays a vital role in the synthesis of proteins (e.g. albumin, clotting factors and complement), detoxification, and storage (e.g. vitamin A). In addition, it participates in the metabolism of lipids and carbohydrates.

• Cirrhosis is often preceded by hepatitis and fatty liver (steatosis). If the cause is removed at this stage, the changes are still fully reversible.

• The pathological hallmark of cirrhosis is the development of scar tissue that replaces normal parenchyma, blocking the portal flow of blood through the organ and disturbing normal function. The development of fibrosis requires several months, or even years, of ongoing injury.

• Recent research shows the pivotal role of the stellate cell, a cell type that normally stores vitamin A, in the development of cirrhosis. Damage to the hepatic parenchyma leads to the activation of the stellate cell, which becomes contractile (called myofibroblast) and obstructs blood flow in the circulation. In addition, it secretes TGF-β₁, which leads to a fibrotic response and proliferation of connective tissue. The extracellular matrix around hepatocytes is composed of collagens (especially type I, III, IV), glycoprotein and proteoglycans.

• Sinusoidal endothelial cells are also important contributor of early fibrosis. Endothelial cells from normal liver produce collagen, laminin and fibronectin.

• In addition, the liver responds to injury with new blood vessels formation. Platelet derived growth factor (PDGF), vascular endothelial growth factor (VEGF), nitric oxide and carbon monoxide are the mediators involved in angiogenesis. Angiogenesis in cirrhosis results in production of immature and permeable VEGF induced neo-vessels thus fails to correct liver injury. ,

• Furthermore, it disturbs the balance between matrix metalloproteinases and the naturally occurring inhibitors (TIMP 1 and 2), leading tomatrix breakdown and replacement by connective tissue-secreted matrix.. Matrix metalloproteinase (MMP) are calcium dependent enzymes that specially degrade collagen and non collagenous substrate. There are five categories of MMP based Upon their specificity for substrate. MMP-2 and stromyelysin-1 are produce from stellate cells. MMP-2 degrades collagen and stromelysin-1 degrades proteoglycan and glycoprotein.

• The fibrous tissue bands (septa) separate hepatocyte nodules, which eventually replace the entire liver architecture, leading to decreased blood flow throughout.
• The spleen becomes congested, which leads to hypersplenism and increased sequestration of platelets.
• Portal hypertension is responsible for most severe complications of cirrhosis.

• Pathogenesis of cirrhosis based upon its individual cause is as following
  • Alcoholic liver disease: Alcohol seems to injure the liver by blocking the normal metabolism of protein, fats, and carbohydrates. Patients may also have concurrent alcoholic hepatitis with fever, hepatomegaly, jaundice, and [[anorexia].
  • Chronic hepatitis C: Infection with hepatitis C virus causes inflammation of and low grade damage to the liver that over several decades can lead to cirrhosis.
  • Non-alcoholic steatohepatitis (NASH): In NASH, fat builds up in the liver and eventually causes scar tissue. This type of hepatitis appears to be associated with diabetes, protein malnutrition, obesity, coronary artery disease, and treatment with corticosteroid medications.
  • Primary sclerosing cholangitis: PSC is a progressive cholestatic disorder presenting with pruritus, steatorrhea, fat soluble vitamin deficiencies, and metabolic bone disease. There is a strong association with inflammatory bowel disease (IBD), especially ulcerative colitis.
  • Autoimmune hepatitis: This disease is caused by the immunologic damage to the liver causing inflammation and eventually scarring and cirrhosis.

Genetics

• Certain TERT gene variant resulting in reduced telomerase activity has been found to be risk factor for sporadic cirrhosis
• An uncharacterised nucleolar protein, NOL11 has a role in the pathogenesis of North American Indian childhood cirrhosis
• Loss of interaction between C-terminus of Utp4/cirhin and other SSU processome protein may cause North American Indian childhood cirrhosis

Gross Pathology

Macroscopically, the liver may be initially enlarged, but with progression of the disease, it becomes smaller. Its surface is irregular, the consistency is firm and the color is often yellow (if associates steatosis). Depending on the size of the nodules there are three macroscopic types: micronodular, macronodular and mixed cirrhosis.

• In micronodular form (Laennec's cirrhosis or portal cirrhosis) regenerating nodules are under 3 mm.
• In macronodular cirrhosis (post-necrotic cirrhosis), the nodules are larger than 3 mm.
• The mixed cirrhosis consists in a variety of nodules with different sizes.

Images courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology

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  Cirrhosis: Gross, external view of micronodular cirrhosis

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  Cirrhosis: Gross, cut section of previous one (an excellent example)

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  Cirrhosis: Gross, close-up image

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  Macronodular cirrhosis and hepatoma

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  Cirrhosis: Gross, close-up, natural color (an excellent example)

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  Cirrhosis: Gross, close-up (an excellent example)

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  Cirrhosis: Gross, close-up view

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  Micronodular cirrhosis: Gross, external view (an excellent example)

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  Micronodular cirrhosis: Gross, close-up image

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  Micronodular cirrhosis: Gross (an excellent example)

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  Macronodular cirrhosis: Gross, natural color (perfect color for cirrhosis), close-up, an excellent example

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  Cirrhosis with portocaval shunt: Gross, severe cirrhosis with extensive liver necrosis due to thrombosis of portocaval shunt (well shown)

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  Endstage cirrhosis: Gross, natural color, close-up (an excellent example)

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  Endstage cirrhosis: Gross, natural color, close-up view is an excellent example for nodules of yellow-orange liver tissue and broad irregular bands of fibrosis

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  Endstage cirrhosis: Gross, natural color, close-up cut surface, very well shown nodules of yellow and necrotic opaque liver tissue with broad and irregular bands of fibrosis (an excellent example)

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  Macronodular cirrhosis: Gross, natural color, external view of liver and very enlarged spleen (liver has variable size nodules up to about 2 cm)

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  Macronodular cirrhosis: Gross, natural color, cut surface, large irregular bands of fibrosis with variable size liver cell nodules up to about 8 mm and all necrotic appears to be an end stage liver disease.

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  Macronodular cirrhosis: Gross, natural color view of frontal sections of liver and spleen showing a contracted macronodular liver and an enlarged spleen as large as the liver

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  Macronodular cirrhosis: Gross, natural color slab of liver

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  Fatty change and early cirrhosis: Gross, natural color, rather close-up image showing typical fatty color, and in lighting at lower right of micrography micronodularity is evident (quite good example)

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  Cirrhosis with portal vein thrombosis: Gross, natural color, sectioned liver with portal vein exposed and filled with red thrombus. A good example of end stage cirrhosis.

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  Endstage cirrhosis with lobular necrosis: Gross, natural color, very close-up view (an excellent example of alcoholic cirrhosis)

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  Micronodular cirrhosis: Gross, natural color view of whole liver through capsule with obvious cirrhosis (note to quite large liver)

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  Micronodular cirrhosis: Gross, natural color, view of whole liver showing external surface typical cirrhotic liver (history of alcoholism)

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  Lung: Idiopathic Interstitial Fibrosis: Gross, natural color, an excellent photo of lung cirrhosis (close-up view)

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  Endstage cirrhosis: Gross, natural color, slice of liver. Portal vein is opened to show size and patency.

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  Endstage cirrhosis: Gross, natural color, severe cirrhosis with bile stasis

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  Portal Vein Thrombosis with cirrhosis: Gross, close-up, micronodular cirrhosis with portal vein thrombosis

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  Lung: Hematite: Gross, natural color, external view of "pulmonary cirrhosis" with typical hematite color

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  Gross, natural color of liver and stomach view from external surfaces, micronodular cirrhosis and hemorrhagic gastritis (as the surgeon would see these in natural color)

Microscopic Pathology

Microscopically, cirrhosis is characterized by regeneration nodules, surrounded by fibrous septa. In these nodules, regenerating hepatocytes are disorderly disposed. Portal tracts, central veins and the radial pattern of hepatocytes are absent. Fibrous septa are important and may present inflammatory infiltrate (lymphocytes, macrophages) If it is a secondary biliary cirrhosis, biliary ducts are damaged, proliferated or distended - bile stasis. These dilated ducts contain inspissated bile which appear as bile casts or bile thrombi (brown-green, amorphous). Bile retention may be found also in the parenchyma, as the so called "bile lakes".

Chronic active hepatitis - Cirrhosis

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Micronodular cirrhosis

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Primary biliary cirrhosis

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