Cirrhosis
By Howard J. Worman, M. D.
What is Cirrhosis?
Cirrhosis is characterized anatomically by widespread nodules in the
liver combined with fibrosis. The fibrosis and nodule formation causes
distortion of the normal liver architecture which interferes with blood
flow through the liver. Cirrhosis can also lead to an inability of the
liver to perform its biochemical functions. To understand the
pathophysiology of cirrhosis, the normal anatomy and physiology of the
liver must first be briefly reviewed.
Liver Blood Flow
Oxygenated blood that has returned from the lungs to the left ventricle
of the heart is pumped to all of the tissues of the body. This is called
the systemic circulation. After reaching the tissues, blood is returned
to the right side of the heart, from where it is pumped to the lungs and
then returned to the left side of the heart after taking up oxygen and
giving off carbon dioxide. This is called the pulmonary circulation.
Blood from the gut and spleen flow to and through the liver before
returning to the right side of the heart. This is called the portal
circulation and the large vein through which blood is brought to the
liver is called the portal vein. After passing through the liver, blood
flows into the hepatic vein, which leads into the inferior vena cava to
the right side of the heart. The liver also receives some blood directly
from the heart via the hepatic artery. In the esophagus, stomach, small
intestine and rectum, the portal circulation and veins of the systemic
circulation are connected. Under normal conditions, there is little to no
back flow from the portal circulation into the systemic circulation.
Bilirubin Secretion
The liver is the site of bile formation. Bile contains bile salts, fatty
acids, cholesterol, bilirubin and other compounds. The components of
bile are synthesized and modified in hepatocytes (the predominant cell
type in the liver) and secreted into small bile ducts within the liver
itself. These small bile ducts form a branching network of progressively
larger ducts that ultimately become the common bile duct that takes bile
to the small intestine. Bilirubin is a yellow pigment that derives
primarily from old red blood cells. Bilirubin is taken up by hepatocytes
from the blood, modified in the hepatocytes to a water soluble form and
secreted into the bile.
Biochemical Functions
The liver performs many biochemical functions. Blood clotting factors
are synthesized in the liver. Albumin, the major protein in the blood,
is also synthesized in and secreted from the liver. The modification
and/or synthesis of bile components also takes place in the liver. Many
of the body's metabolic functions occur primarily in the liver including
the metabolism of cholesterol and the conversion of proteins and fats
into glucose. The liver is also where most drugs and toxins, including
alcohol, are metabolized.
What Goes Wrong in Cirrhosis?
Cirrhosis results from damage to liver cells from toxins, inflammation,
metabolic derangements and other causes. Damaged and dead liver cells
are replaced by fibrous tissue which leads to fibrosis (scarring). Liver
cells regenerate in an abnormal pattern primarily forming nodules that
are surrounded by fibrous tissue. Grossly abnormal liver architecture
eventually ensues that can lead to decreased blood flow to and through
the liver.
Decreased blood flow to the liver and blood back up in the portal vein
and portal circulation leads to some of the serious complications of
cirrhosis. Blood can back up in the spleen causing it to enlarge and
sequester blood cells. Most often, the platelet count falls because
of splenic sequestration leading to abnormal bleeding. If the pressure
in the portal circulation increases because of cirrhosis and blood back
up (note: this can also sometimes occur in severe cases of acute
hepatitis and liver damage), blood can flow backwards from the portal
circulation to the systemic circulation where they are connected. This
can lead to varicose veins in the stomach and esophagus (gastric and
esophageal varices) and rectum (hemorrhoids). Gastric and esophageal
varices can rupture, bleed massively and even cause death. Hypertension
in the portal circulation, along with other hormonal, metabolic and
kidney abnormalities in cirrhosis, can also lead to fluid accumulation
the abdomen (ascites) and the peripheral tissue (peripheral edema).
Decreased bilirubin secretion from hepatocytes in cirrhosis leads to the
back up of bilirubin in the blood. This leads to jaundice, the yellow
discoloration of the skin and eyes. As the water-soluble form of
bilirubin also backs up in the blood, bilirubin can also spill into the
urine giving it a bright yellow to dark brown color.
Abnormal biochemical function of the liver in cirrhosis can lead to
several complications. The serum albumin concentration falls which can
lead to aggravation of ascites and edema. The metabolism of drugs can
change requiring dose adjustments. In men, breast enlargement
(gynecomastia) sometimes occurs because metabolism of estrogen in the
liver is decreased. Decreased production of blood clotting factors can
lead to bleeding complications. Derangements in the metabolism of
triglycerides, cholesterol and sugar can occur. In earlier stages,
cirrhosis frequently can cause insulin resistance and diabetes mellitus.
In later stages or in severe liver failure, blood glucose may be low
because it cannot be synthesized from fats or proteins.
Cirrhosis, especially in advanced cases, can cause profound abnormalities
in the brain. In cirrhosis, some blood leaving the gut bypasses the
liver as blood flow through the liver is decreased. Metabolism of
components absorbed in the gut can also be decreased as liver cell
function deteriorates. Both of these derangements can lead to hepatic
encephalopathy as toxic metabolites, normally removed from the blood by
the liver, can reach the brain. In its early stages, subtle mental
changes such as poor concentration or the inability to construct simple
objects occurs. In severe cases, hepatic encephalopathy can lead to
stupor, coma, brain swelling and death.
Cirrhosis of the liver can also cause abnormalities in other organ
systems. Cirrhosis can lead to immune system dysfunction causing an
increased risk of infection. Ascites fluid in the abdomen often becomes
infected with bacteria normally present in the gut (spontaneous bacterial
peritonitis). Cirrhosis can also lead to kidney dysfunction and
failure. In end-stage cirrhosis, a type of kidney dysfunction called
hepatorenal syndrome can occur. Hepatorenal syndrome is almost always
fatal unless liver transplantation is performed.
Clinical Symptoms and Diagnosis of Cirrhosis
Cirrhosis is usually an easy diagnosis to make when any or all of the
above abnormalities and complications are present. This is especially
true when the underlying liver disease can be identified. The underlying
liver disease (see below) is identified in most patients, however,
sometimes it will not be discovered. Such cases are called "cryptogenic"
cirrhosis. Sometimes, other conditions such as metastatic cancer,
hepatic or portal vein thrombosis, severe acute hepatitis or acute bile
duct obstruction can cause some of the abnormalities seen in cirrhosis.
A careful history combined with special diagnostic tests will usually
identify these conditions.
Some patients with cirrhosis, especially early in the course of the
disease, will have no overt clinical signs or symptoms. Some may have
only subtle physical changes such as red palms, red spots that blanch on
their upper body (spider angiomata), hypertrophy of the parotid glands,
gynecomastia or fibrosis of tendons in the palms. Some patients may only
have subtle abnormalities on blood tests, and in some cases, all blood
tests may be normal. Radiological and nuclear medicine tests may give
clues as to the presence of cirrhosis, but the diagnosis of cirrhosis
must often be made by liver biopsy.
Causes of Cirrhosis
Although most often associated with alcohol abuse, cirrhosis of the liver
can result from many causes. Almost any chronic liver disease can lead
to cirrhosis. This list gives some of the many causes:
- Alcoholic liver disease - most common
cause in the U. S. A.
- Chronic viral hepatitis B, C and D
- Chronic autoimmune hepatitis
- Inherited metabolic diseases (e. g. hemochromatosis, Wilson disease)
- Chronic bile duct diseases (e. g. primary
biliary cirrhosis)
- Chronic congestive heart failure
- Parasitic infections (e. g. schistosomiasis)
- Nonalcoholic steatohepatitis (liver inflammation that can be caused by fatty liver)
- Long term exposure to toxins or drugs
Treatment
Cirrhosis of the liver is irreversible but treatment of the underlying
liver disease may slow or stop the progression. Such treatment depends
upon the underlying etiology. Termination of alcohol intake will stop
the progression in alcoholic cirrhosis and for this reason, it is
important to make the diagnosis early in a chronic alcohol abuser.
Similarly, discontinuation of a hepatotoxic drug or removal of an
environmental toxin will stop progression. Treatment of metabolic
diseases, such as treatment of iron overload in hemochromatosis or copper
overload in Wilson disease, are also effective therapies. Chronic viral
hepatitis B and C may respond to treatment with interferon and autoimmune hepatitis may improve with
prednisone and azathioprine (Imuran). Drugs such as ursodiol (Actigall)
may slow the progression of primary biliary cirrhosis and possibly sclerosing
cholangitis.
In patients with cirrhosis of the liver, treatment must also be directed
at the complications. Bleeding esophageal varices can be treated with
endoscopic sclerotherapy or rubber band ligation. Ascites and edema are
often responsive to a
low sodium diet and such a diet must be emphasized in patients with these
symptoms. More advanced ascites and edema can respond to diuretic
therapy. A low protein diet and agents such as lactulose may help
hepatic encephalopathy. Infections such as spontaneous bacterial
peritonitis must be rapidly treated with appropriate antibiotics. Drugs
metabolized in the liver must be given with caution. Coagulation
disorders will sometimes respond to vitamin K.
Liver transplantation is highly effective for the treatment of end-stage
cirrhosis. Transplantation is usually needed when complications such as
encephalopathy, ascites or bleeding varices are uncontrollable or when
biochemical function is severely depressed. In patients with primary
biliary cirrhosis, a rising bilirubin indicates a poor prognosis and such
patients should be considered for transplantation as the serum
bilirubin concentration begins to rise. Active drug or alcohol abuse
are contraindications to liver transplantation. However, alcoholics who
have abstained from drinking for an extended period of time (usually more
than six months), and have participated in rehabilitation programs and
support groups such as Alcoholics Anonymous, can be considered as
candidates and will often have a good prognosis. Liver cancer is usually
a contraindication to transplantation, except in experimental protocols.
Liver transplantation is usually not performed in patients more than 70 years
old.
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Copyright, 1995, 1998, 2000, Howard J. Worman, M. D. All rights
reserved. Printing or other reproduction is prohibited without the
written authorization of Howard J. Worman.