hepatitis & cirrhosis dr. gehan mohamed dr. abdelaty shawky

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Hepatitis & Hepatitis & Cirrhosis Cirrhosis Dr. Gehan Mohamed Dr. Dr. Gehan Mohamed Dr. Abdelaty Shawky Abdelaty Shawky

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Page 1: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Hepatitis & CirrhosisHepatitis & Cirrhosis

Dr. Gehan Mohamed Dr. Abdelaty ShawkyDr. Gehan Mohamed Dr. Abdelaty Shawky

Page 2: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Learning objectives

Understand the normal Liver Functions so can predict what is the clinical picture when liver failure occur.

Recognize definition of hepatitis and discuss its types(Acute, Chronic, Fulminant).

List different Causes and Patterns of hepatitis .

- Understand the differences between different types of viral hepatitis regarding Transmisson, Carrier state, Chronicity.

List the cellular changes in both Acute and chronic Hepatitis.

Page 3: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Learning objectives

Understand difference between chronic hepatitis and fulminant hepatitis.

Discuss definition ,etiology of cirrhosis and its variable gross pictures.

discuss the Pathogenesis of Hepatic Encephalopathy.

Page 4: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

HepatitisHepatitis

* Definition:

Hepatitis is necro-inflammatory liver disease characterized by the presence of inflammatory cells in in the portal tracts then spillover to neighboring parynchmatous liver cells .

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Normal liver

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Hepatitis

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* Causes of hepatitis:* Causes of hepatitis:1. Viral: hepatotropic (A, B, C, D….) and non-hepatotropic (cytomegalovirus and Epstein bar virus).

2. Alcoholic.

3. immune mediated: autoimmune hepatitis.

4. Drug induced.

5. Metabolic disorders: Hemochromatosis (due to iron accumulation) and Wilsons disease (copper accumulation) can cause liver inflammation and necrosis.

Page 8: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

6. Other causes:

Biliary obstruction by gall stones .

ischemic hepatitis associating shock.

giant cell hepatitis ,common in children may be due to viral infection.

Page 9: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Virus Hep-A Hep-B Hep-C

agent RNA DNA RNATransmisson. Feco-oral Parenteral

-maternal to fetal

-sexual

-drug abusers

- Parenteral

-maternal to fetal

-Sexual

-drug abusers

Carrier state

None 0.1-1.0% 0.2-1.0%

Chronic Hepatitis

None 5-10% >50%

Page 10: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Patterns of hepatitisPatterns of hepatitis

Carrier state: is an individual who harbor and can transmit the virus but has no manifest symptoms.

Acute hepatitis: hepatitis is considered acute if its manifestation persist for period less than six months.

Chronic hepatitis: hepatitis is considered chronic if there is clinical or seriological evidence of liver pathology persistent for more than six consequent months.

Fulminant hepatitis: hepatitis is considered fulminant if massive hepatic cell necrosis happened within few weeks leading to acute hepatic failure and hepatic encephalopathy.

Page 11: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Acute Viral HepatitisAcute Viral Hepatitis

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Diagnosis of acute hepatitisDiagnosis of acute hepatitis

1. Clinical picture.

2. Laboratory investigations.

3. Histopathologic diagnosis of liver biopsy.

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1. Clinical picture of acute viral hepatitis (AVH):1. Clinical picture of acute viral hepatitis (AVH):

AVH is more likely to be asymptomatic in younger people.

If AVH is symptomatic, it may be either non specific or specific symptoms.

Initial features are of nonspecific flu-like symptoms include malaise, muscle and joint aches, fever, nausea or vomiting, diarrhea, loss of appetite, and headache.

More specific symptoms and signs are: yellow color of the eyes and skin (i.e., jaundice) and abdominal discomfort from hepatomegaly (swelling of the liver).

Page 14: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

jaundice

Page 15: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

2. Laboratory investigations of AVH:2. Laboratory investigations of AVH:1. Ultrasound examination to detect any biliary stones, hepatomegaly.

2. Serologic examination to detect :

a- Elevated hepatic enzymes as

- aspartate aminotransferase(AST)

- alanine aminotransferase(ALT).

b- Viral hepatitis markers as HBV sAg, HCV Antigen and Antibody

c- Autoantibodies as in case of autoimmune hepatitis.

d- Polymerase chain reaction(PCR) to identify the virus.

Page 16: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

3. Histopathology of AVH:3. Histopathology of AVH:

The normal liver architecture is usually preserved.

Inflammatory cellular infiltrate (plasma cells, lymphocytes and neutrophils) inside portal tracts and around foci of necrosis.

The hepatocytes show:

Apoptosis: the cells appear acidophilic (Councilman bodies).

Hydropic degeneration.

Cholestasis means accumulation of bile in liver cells even canalicular bile plugs can be formed in cases of hepatitis caused by biliary obstruction by stones.

Hepatocyte regeneration.

Page 17: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Acute - Hepatitis - Chronic

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Liver Biopsy – Chronic Hepatitis: the inflammatory cells are present in portal tract and in periportal areas

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Councilman bodies are eosinophilic dead apoptotic liver cells

Page 20: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Cholestasis: accumlation of bile inside hepatocytes

Page 21: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Chronic hepatitisChronic hepatitis

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* Clinical picture of Chronic hepatitis:

Often no symptoms at all.

It is commonly identified on blood tests performed either for screening or to evaluate nonspecific symptoms.

nonspecific symptoms such as malaise, tiredness and weakness.

The occurrence of jaundice indicates advanced liver damage.

On physical examination there may be enlargement of the liver

Page 23: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

* Histopathology for chronic hepatitis:

I. Portal tracts show:

a. Piece meal necrosis: necrosis of the hepatocytes at the limiting plate.

b. Portal tract inflammation:

mononuclear inflammatory cells; lymphocytes, macrophages with occasional plasma cells.

Lymphoid follicle formation (with HCV).

Bile duct inflammation (with HCV).

Page 24: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

II. The hepatic lobules show:

Degeneration: Fatty change (with HCV).

Necrosis:

Focal (spotty) necrosis surrounded by inflammatory cells.

Confluent necrosis and bridging necrosis: with progressive hepatitis.

Dysplasia of hepatocytes (precancerous).

Von Kupffer cell hyperplasia.

Page 25: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Specific diagnostic lesions:

• Ground glass appearance of hepatocytes (with HBV).

• Presence of cupper particles inside the hepatocytes (with Wilson disease).

• Rosseting: occasional arrangement of a group of hepatocytes around a central bile canaliculus. Characteristic of auto-immune hepatitis.

III. Fibrosis & Cirrhosis.

Page 26: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Grading of chronic hepatitis by assessing the degree of activity: this is done by examining 4 parameters; portal inflammation, piece meal necrosis, focal (spotty) necrosis and confluent necrosis. The degree of activity is graded as mild, moderate and marked according to the score of these parameters.

Staging of chronic hepatitis by assessment of the degree of fibrosis

Page 27: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

chronic hepatitis with piece meal necrosis

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Histopathology show ground glass hepatocytes, which are seen in chronic hepatitis B infections represent accumulations of viral

antigen in the endoplasmic reticulum. H&E

Page 29: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Histopathology show lymphoid aggregates and fatty change of the hepatocytes, which are characteristically

seen in chronic hepatitis C infections

Page 30: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Liver cirrhosisLiver cirrhosis

Page 31: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

* Definition:

Chronic Diffuse, irreversible disorder of the liver characterized by;

1.Liver cell degeneration and necrosis.

2.Replaced by extensive fibrosis .

3.Compensatory hyperplasia of the remaining healthy liver cells leading to the formation of the Regenerating parenchymal nodules.

4.Complete loss of normal architecture.

Page 32: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

* Etiological classification of Cirrhosis:

A. Congenital cirrhosis:A. Congenital cirrhosis:

1. Congenital syphilis.

2. Hemochromatosis.

3. Glycogen storage disease.

4. Wilson disease.

5. α1 antitrypsin deficiency.

Page 33: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

B. Acquired cirrhosis:B. Acquired cirrhosis:

1. Post-hepatitic (viral).

2. Alcoholic.

3. Biliary cirrhosis.

4. Cirrhosis caused by circulatory disorders e.g. chronic right sided heart failure.

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* Complications of Cirrhosis: * Complications of Cirrhosis:

1. Liver cell Failure

2. Portal hypertension

3. Hepatocellular carcinoma.

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Normal Liver

Page 36: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Micronodular cirrhosis

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Macronodular Cirrhosis

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Normal Liver Histology

CV

PT

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Liver Biopsy – Cirrhosis

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Liver Biopsy – Cirrhosis:

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Liver cell failureLiver cell failure

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* Normal Liver Functions:* Normal Liver Functions:

Metabolism – Carbohydrate, Fat & Protein.

Secretory – bile, Bile acids, salts.

Excretory – Bilirubin, drugs, toxins.

Synthesis – Albumin, coagulation factors.

Storage – Vitamins, carbohydrates etc.

Detoxification – toxins, ammonia, etc.

Page 43: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

* Manifestations of liver cell failure* Manifestations of liver cell failure

1. Jaundice: yellow colour of skin ,mucosa due to hyperbilirubinemia as liver became unable to conjugate bilirubin so it not secreted in urine and so it is reabsorbed by blood and precipitate in tissues.

2. Coagulopathy:→ bleeding tendency

3. Hypoproteinemia specially albumin → decrease osmotic pressure of blood → generalized edema

.

Page 44: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

4. Hepatic Encephalopathy: caused by the inability of the liver to detoxify amonia which produced by effect of intestinal bacteria on food so this amonia can affect brain causing coma.

5. Hyperestrogenemia due to decrease estrogen degradation by the diseased liver leading to gynaecomastia and testicular atrophy in males

Page 45: Hepatitis & Cirrhosis Dr. Gehan Mohamed Dr. Abdelaty Shawky

Gynaecomastia in cirrhosis i.e. enlargement of male breast due to failure of degradation of estrogen by the

diseased liver.

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Portal hypertensionPortal hypertension

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Portal hypertension leading to;

1. Varices: esophageal varices, piles.

2. Splenomegaly due to splenic congestion.

3. Ascites which is accumulation of transudate in the peritoneal cavity.

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Ascitis in Cirrhosis

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CirrhosisClinical

Features

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