Liver Conditions

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Vocabulary practice flashcards covering liver pathophysiology, viral hepatitis types, cirrhosis, clinical manifestations, complications, diagnostics, and interprofessional treatments from ATI Chapter 56.

31 Terms

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Hepatitis

Inflammation of the liver caused most commonly by viruses (A, B, C, D, E), as well as alcohol, medications, toxic chemicals, autoimmune diseases, and metabolic abnormalities.

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Hepatitis A Virus (HAV)

A form of viral hepatitis transmitted primarily through eating contaminated food or drinking contaminated water (fecal-oral route), prevented by good hygiene and vaccination, with no specific antiviral drug therapy required.

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Hepatitis B Virus (HBV)

A bloodborne and sexually transmitted viral hepatitis spread through contact with infected blood or bodily fluids; preventable via vaccination and blood screening, and treated when severe with alpha interferon or peginterferon.

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Hepatitis C Virus (HCV)

A viral infection spread exclusively through blood-to-blood contact that lacks a vaccine but can be effectively cured (>98%> 98\% cure rate) using direct-acting antiviral (DAA) medications.

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Hepatitis D Virus (HDV)

A bloodborne virus that causes infection solely in individuals who are already infected with Hepatitis B, prevented by the Hepatitis B vaccine and treated with interferon.

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Hepatitis E Virus (HEV)

A viral liver infection transmitted by ingesting water or food contaminated with feces, prevented through good hygiene and safe water consumption, which requires no specific medical treatment.

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<p>Jaundice (Icterus)</p>

Jaundice (Icterus)

A yellowish discoloration of the skin and sclera resulting from elevated serum bilirubin levels during acute or advanced liver dysfunction, often accompanied by dark urine, clay-colored stools, and pruritus.

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Convalescent Phase (Acute Hepatitis)

The recovery phase of acute viral hepatitis lasting 2 to 4 months2\text{ to }4\text{ months}, beginning as jaundice resolves, where major complaints include malaise and easy fatigability while hepatomegaly persists.

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Asterixis

A rapid, motor flapping tremor of the hands and arms (termed 'liver flap') caused by neurotoxic accumulation of ammonia in hepatic encephalopathy.

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Apraxia

A neurologic manifestation of hepatic encephalopathy resulting in impaired constructional ability, specifically making it difficult for the patient to write or move a pen from left to right.

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Fetor Hepaticus

A sweet, musty odor on the patient's breath caused by metabolic byproducts that the failing liver is unable to detoxify.

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<p>Palmar Erythema</p>

Palmar Erythema

Redness over the palmar surfaces of the hands, commonly observed in chronic liver failure and cirrhosis due to circulating endocrine alterations.

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<p>Spider Angioma</p>

Spider Angioma

Small, dilated blood vessels with a central red point and radiating spider-like branches appearing on the face, neck, upper chest, and arms in chronic liver disease.

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<p>Liver Biopsy</p>

Liver Biopsy

The gold standard and most definitive diagnostic procedure for liver disease, where a tissue core is extracted needle-biopsy style, requiring midnight fasting prior and post-procedure right side-lying positioning for several hours.

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<p>Ultrasound Elastography (FibroScan)</p>

Ultrasound Elastography (FibroScan)

A non-invasive diagnostic ultrasound study used to assess liver stiffness, fibrosis, and cirrhosis development.

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Cirrhosis

An end-stage chronic liver condition characterized by extensive degeneration and destruction of hepatocytes, resulting in replacement with disorganized fibrous bands and regenerative nodules.

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Compensated Cirrhosis

Early-stage cirrhosis where the liver continues to function adequately; the patient presents with few early symptoms (such as fatigue or an enlarged liver) and may exhibit normal liver function tests.

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Decompensated Cirrhosis

Advanced liver disease defined by the appearance of one or more serious complications, including portal hypertension, esophageal and gastric varices, peripheral edema, ascites, hepatic encephalopathy, or hepatorenal syndrome.

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Primary Biliary Cirrhosis (PBC)

A form of biliary cirrhosis caused by chronic progressive inflammation and destruction of intrahepatic bile ducts.

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Primary Sclerosing Cholangitis (PSC)

An autoimmune disorder in which the immune system mistakenly attacks, scars, and narrows the bile ducts, predisposing the patient to biliary cirrhosis.

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Cardiac Cirrhosis

Liver fibrosis and necrosis resulting from severe, long-standing right-sided heart failure causing chronic hepatic venous congestion.

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Portal Hypertension

An abnormally elevated venous blood pressure within the portal venous system leading to splenomegaly, collateral vein formation, ascites, and gastrointestinal varices.

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Collateral Circulation

Alternate circulatory pathways developed to decompress portal venous hypertension, developing distended veins (varicosities) in areas like the lower esophagus, anterior abdominal wall, peritoneum, and rectum.

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Caput Medusae

A visible ring of dilated, tortuous collateral veins radiating around the umbilicus, formed as a consequence of severe portal hypertension.

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Esophageal and Gastric Varices

Fragile, distended collateral veins in the lower esophagus or stomach that rupture and bleed easily, representing the most life-threatening complication of portal hypertension.

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<p>Ascites</p>

Ascites

The abnormal accumulation of serous fluid inside the peritoneal cavity due to portal hypertension, hypoalbuminemia, and hyperaldosteronism, often causing marked abdominal distention.

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<p>Balloon Tamponade</p>

Balloon Tamponade

A mechanical intervention utilizing multi-lumen inflatable tubes (such as the Sengstaken-Blakemore or Minnesota tube) to compress bleeding esophageal and gastric varices directly.

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<p>Transjugular Intrahepatic Portosystemic Shunt (TIPS)</p>

Transjugular Intrahepatic Portosystemic Shunt (TIPS)

A nonsurgical interventional radiological procedure that places a metal stent between the portal vein and hepatic vein to relieve portal hypertension and recurrent bleeding.

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Hepatorenal Syndrome

Functional renal failure occurring in end-stage cirrhosis marked by azotemia, oliguria, intractable ascites, and renal vasoconstriction without intrinsic structural kidney defects, curable primarily via liver transplantation.

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Hepatic Encephalopathy

A neuropsychiatric syndrome secondary to liver disease and toxic circulating ammonia levels that cross the blood-brain barrier, causing altered consciousness, confusion, agitation, asterixis, and coma.

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Lactulose

A medication that prevents constipation and lowers blood ammonia levels by acidifying colon contents and trapping ammonia in the gut to facilitate excretion.