Page 217 - Physiology and Pathophysiology MNU 2024-2025 نظرى
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Clinical pharmacy 2024/2025                  Level 2 Pharm D                       Physiology and Pathophysiology (MD303)
            ▪  Jaundice:

            o  Yellowing of the skin and whites of the eyes due to excess levels of circulating bilirubin.
            o  Bilirubin is the pigment portion of bile. Bilirubin is formed from hemoglobin during the normal
               and abnormal breakdown of RBCs.
            o  Free bilirubin formed in the blood is conjugated by the liver and eliminated into the intestinal
               tract along with bile.
            o  Any condition that impairs the ability of the liver to conjugate and eliminate bilirubin will result in
               the accumulation of bilirubin in the blood with the occurrence of jaundice.


                                          ❖  Possible complications of hepatitis:
            1.  Chronic active or persistent hepatitis can lead to progressive liver injury, liver failure and death.
            2.  Chronic active hepatitis is also associated with an increased incidence of hepatocellular carcinoma.

        2- Cirrhosis:
            ▪  Cirrhosis  is  a  general  term  referring  to  destruction  of  normal  liver
               structure.
            ▪  Cirrhosis is characterized by diffuse scarring and fibrosis of the liver in

               response to chronic inflammation and injury.
            ▪  One of the major features of cirrhosis is the replacement of functional
               liver tissue by scar tissue.
            ▪  The most prevalent cause of liver cirrhosis is alcohol abuse.
                                               ❖  Types of Liver Cirrhosis:
        1- Alcoholic cirrhosis: Caused by excess ethanol intake, and possible acetaldehyde toxicity (a metabolite
            of ethanol)
        2- Biliary cirrhosis: Caused by: bile duct obstruction.

        3- post-necrotic cirrhosis: Caused by: viral hepatitis or exposure to drugs or toxins
        4- Metabolic Cirrhosis: caused by:
           •  Glycogen  Storage  Disease:  is  a metabolic  disorder  caused  by enzyme  deficiencies  affecting
               either glycogen synthesis or glycogen breakdown
           • Wilson disease: is a rare inherited disorder that causes copper to accumulate in your liver, brain and
               other vital organs.
           • Galactosemia: is a rare genetic metabolic disorder that affects an individual's ability to metabolize
               the sugar galactose

                              ❖  Alcoholic liver disease presents in three progressive stages:

           1- Alcoholic steatosis: “Fatty liver.”
            • Accumulation of fat in the hepatocytes.
            • May occur as a result of altered fat metabolism in the liver.
            • Changes include increased synthesis of fatty acids and
                 triglycerides.

            • Enlargement of the liver is accompanied by anorexia, nausea,
                 and jaundice.
        • At this point the fatty changes are generally reversible if alcohol consumption ceases.


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