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LIVER

Pathology REYES OT

QuestionAnswer
Which of the following cells found within the liver is the major source of the excess collagen deposited in cirrhosis? ● Hepatocytes ● Kupffer Cells ● Ito Cells ● Endothelial Cells ● Bile duct epithelial Cells Ito Cells Hepatic stellate cells (HSC), also known as perisinusoidal cells or Ito cells (earlier lipocytes or fat-storing cells), are pericytes found in the perisinusoidal space of the liver, also known as the space of Disse.
All of the ff produced a predominantly unconjugated hyperbilirubinemia EXCEPT: ● Hemolytic anemias ● Physiologic jaundice of the newborn ● Crigler-Najjar syndrome, type 1 ● Gilbert's syndrome ● Dubin-Johnson syndrome Dubin-Johnson syndrome Predominantly Conjugated Hyperbilirubinemia -Decreased hepatic excretion of bilirubin glucuronides -Deficiency in canalicular membrane transporters (Dubin-Johnson syndrome, Rotor syndrome)
Dilated sinusoids and irregular cystic spaces filled with blood within the liver, which may rupture leading to massive intra-abdominal hemorrhage, are most common associated with: ● Salicylates ● Estrogen ● Anabolic steroids ● Acetaminophen Anabolic steroids Peliosis Hepatis  primary dilation of hepatic sinusoids associated with exposure to anabolic steroids, oral contraceptives, and danazol  liver is mottled and blotchy  irregular blood-filled cystic spaces, with or without lining endothelium
Refers to a severe clinical consequence of liver disease and develops only with loss of >80-90% of hepatic function Hepatic failure  a severe clinical consequence of liver disease and develops only with loss of >80-90% of hepatic function  overall mortality is 70-95%
Which viral hepatitis does not cause chronic disease or the carrier state? Hepatitis A  does not cause chronic disease or the carrier state  acute infection is marked by anti-HAV IgM in serum, IgG can persist for years conferring immunity
All of the following viral hepatitis infections cause hepatocellular carcinoma EXCEPT: ● Hepatitis A infection ● Hepatitis B infection ● Hepatitis C infection ● Hepatitis D infection ● Hepatitis G infection Hepatitis A Of the primary hepatitis viruses, only hepatitis B and C viruses cause HCC. Hepatitis A and E viruses do not produce long-term pathological sequelae. Although HDV always occurs as co-infection with HBV and leads to severe acute or chronic hepatic disease.
All of the following are inherited anomalies of the biliary tree EXCEPT: ● von-Meyenburg complex ● Polycystic liver disease ● Congenital hepatic fibrosis ● Budd-Chiari syndrome ● Caroli disease Budd-Chiari syndrome Budd-Chiari syndrome [Hepatic vein thrombosis] - HEPATIC VEIN OUTFLOW OBSTRUCTION
The most common hepatic malignancy Hepatocellular carcinoma
All of the following are risk factors for cholesterol gallstone formation EXCEPT: ● Americans ● Gallbladder stasis ● Biliary tract infections ● Hypercholesterolemic syndromes ● Oral contraceptive use Biliary tract infections Native Americans, adults in industrialized countries Increasing age, with male:female ratio of 1:2 Estrogenic influences, clofibrate, obesity, or rapid weight loss Gallbladder stasis (e.g.spinal cord injury or pregnancy) Hypercholesterolemic syndromes
Antibodies to which of the following forms of viral hepatitis do not confer immunity from reinfection? Hepatitis C elevated titers of anti-HCV IgG do not confer effective immunity, either against reactivation of endogenous HCV or by infection with a new HCV strain
Chronic hepatitis is most likely to occur after acute infection with which of the following viruses? ● Hepatitis A virus ● Hepatitis B virus ● Hepatitis C virus ● Hepatitis E virus ● Coinfection with Hepatitis B & D virus Hepatitis C  high rate of progression to chronic disease and cirrhosis (>50%)  high risk of developing hepatocellular carcinoma  persistent infection and chronic hepatitis are the hallmarks of HCV infection
Which of the following conditions is least likely to be seen in association with cholelithiasis in a 38-year-old female? ● Adenocarcinoma of the gallbladder ● Obesity ● Hemolytic anemia ● Crohn disease ● Chronic hepatitis B Chronic hepatitis B
Hepatic circulatory disorders characterized by impaired intrahepatic blood flow. Cirrhosis IMPAIRED INTRAHEPATIC BLOOD FLOW  cirrhosis is the most important cause  sinusoidal occlusion leading to parenchymal necrosis include DIC, sickle cell disease, and sarcoidosis
This type of intrahepatic biliary tract disease is associated with Inflammatory Bowel Disease ( particularly ulcerative colitis. Primary sclerosing cholangitis Etiology Unknown, possibly autoimmune; 50%-70% associated with inflammatory bowel disease
Carcinoma of the gallbladder is associated with all of the following statements. EXCEPT: ● The most important risk factor for gallbladder carcinoma is gallstones ● It is the most common malignancy of the extrahepatic biliary tract [flip other options] ● Most common gallbladder carcinomas are adenocarcinoma ● Carries an excellent prognosis because gallbladder carcinoma is typically detected early ● Gallbladder carcinoma is at least twice as common in women than in men [options done] ● Carries an excellent prognosis because gallbladder carcinoma is typically detected early
All of the following statements are true of Hepatitis B Virus Infection. EXCEPT: ● A characteristic feature is the high mortality rate among pregnant women. approaching 20% ● It can produce progressive chronic disease ending in cirrhosis [flip next] ● HBx protein has been implicated in the pathogenesis of hepatocellular carcinoma ● HBe antigen, HBV-DNA and DNA polymerase signify active viral replication ● Age at the time of infection is the best predictor of chronicity [options done]
Alcoholic liver disease is characterized by the following EXCEPT: ● Consumption of 80 grams/day of alcohol is considered to be the threshold for the development of ALD ● Fatty change is completely reversible if there is abstinence from alcohol intake ● Alcoholic hepatitis is characterized by hepatocyte swelling and necrosis, Mallory bodies, and neutrophilic reaction ● 50% of alcoholics develop cirrhosis ● The development of severity of ALD are also influence by other factors ● Alcoholic hepatitis is characterized by hepatocyte swelling and necrosis, Mallory bodies, and neutrophilic reaction (hepatocyte swelling and apoptosis dapat)
Diagnosis of this Hepatitis Virus is by third-generation ELISA for antibody detection and PCR for Hepatitis Virus RNA. Hepatitis C Virus Diagnosis for HCV ELISA for HCV antibodies; PCR for HCV RNA
The most common hepatotoxin causing acute liver failure is: Acetaminophen A classic, predictable hepatotoxin is acetaminophen, now the most common cause of acute liver failure necessitating transplantation in the United States.
This inherited metabolic liver disease is characterized by a mutation in metal ion transporter ATP7B gene. Wilson disease Wilson disease is caused by loss-of-function mutations in the metal ion transporter ATP7B, which results in accumulation of copper in the liver, brain (particularly basal ganglia), and eyes (Kayser-Fleischer rings).
A 49-year-old male experiences increasing ascites, and a liver biopsy demonstrates diffuse portal tract bridging fibrosis and nodular regeneration of liver cells. There is no hepatocyte necrosis and no cholestasis. Within the areas of fibrosis, bile duct proliferation and mononuclear cell inflammatory infiltrates can be seen. These findings are most characteristic for: Cirrhosis
The finding of multiple, pale yellow, hard, round stones within the gallbladder is associated with all of the following EXCEPT: [flip for options] ● Oral contraceptives ● Obesity ● Biliary infection population ● Hyperlipidemia syndromes ● Prevalence within the Native-American [flip for answer] Biliary infection population
Which of the following modes of transmission of HBV is most likely to give rise to a carrier state? Vertical transmission during childbirth
A 38-year-old woman complains of fatigue and pruritus. She is found to have high serum alkaline phosphatase and slightly elevated serum bilirubin levels, and serum antimitochondrial antibodies are present. The most likely diagnosis is: Primary biliary cirrhosis LABORATORY FINDINGS Same as secondary biliary cirrhosis, plus elevated serum IgM autoantibodies (especially M2 form of anti-mitochondrial antibody)
A 59-year old male, chronic alcoholic was brought to the emergency room due to vomiting of blood. The patient is jaundiced with elevated liver enzymes. A liver biopsy was performed, the microscopic findings are [cont question] Delicate bands or broad septa accompanied by reorganization of the vascular architecture, with formations of abnormal interconnections between inflow and outflow What is your diagnosis? Liver cirrhosis
All of the following conditions are major clinical consequences of portal hypertension in the setting of the above condition. EXCEPT: ● Hepatic encephalopathy ● Hepatomegaly ● Splenomegaly ● Esophageal varices ● Ascites Hepatomegaly The four major consequences of portal hypertension are (1) hepatic encephalopathy (described under liver failure), (2) ascites, (3) the formation of portosystemic venous shunts, and (4) congestive splenomegaly.
A 58-year old woman consulted a private clinic due to jaundice, skin xanthomas, diarrhea, and pruritus of prolonged duration. Alkaline phosphatase and gamma glutamyl transferase are elevated. Liver biopsy was performed Hepatocytes are enlarged with dilated canalicular spaces. Apoptotic cells may be seen, and Kupffer cells frequently contained regurgitated bile pigments. Cholestasis
All are morphologic features of the above liver biopsy, EXCEPT: ● Enlarged hepatocytes ● Absence of neutrophilic inflammation ● Presence of apoptotic cells ● Kupffer cells containing regurgitated bile ● Bile duct proliferation Absence of neutrophilic inflammation All of the following are morphologic features of the above liver biopsy, EXCEPT:
A 48-year old male, chronic alcoholic consulted at the OPD due to an ill- defined upper abdominal mass, abdominal pain, malaise, fatigue, and weight loss. Liver enzymes, direct bilirubin and a-feto protein are all elevated. What is your diagnosis. Hepatocellular carcinoma
All of the following statements are true of Hepatocellular Carcinoma (HCC) EXCEPT: A. Precursor lesions in HCC are biliary intraepithelial neoplasia, mucinous cystic neoplasms, and papillary biliary neoplasia B. HCC is the most common primary liver cancer C. Chronic liver diseases are the most common setting for the emergence of HCC D. The most important underlying factors in hepatocarcinogenesis are viral infections and toxic injuries E. Activation of ß-catenin and inactivation of p53 are the 2 most common mutations in HCC A ang sagot [EXCEPT ha}
A 48-year-old female presents w/ colicky RUQ pain. He has had nausea for the past 2 days. His temp is now 38.8C. His WBC count is 11.200/uL. with a differential count of 71 segmented neutrophils, 9 band cells. 13 lymphocytes, and 7 monocytes per 100 WBCs. ● Acute cholecystitis with cholecystolithiasis ● Acute cholecystitis with choledocholithiasis ● Chronic cholecystitis with cholecystolithiasis ● Chronic cholecystitis with choledocholithiasis ● Cholesterolosis Acute cholecystitis with cholecystolithiasis
Major risk factors for the development of the above lesion include all of the following, EXCEPT: [pigmented gallstones] ● Ileal diseases ● Oral contraceptives ● Biliary infections ● Chronic hemolytic syndromes ● Rural more than urban Oral contraceptives  Asian more than Western, rural more than urban  chronic hemolytic syndromes or biliary tract infections  ileal disease (resection or bypass) or cystic fibrosis with pancreatic insufficiency
COLUMN A Cholangiocarcinoma Chronic Cholecystitis Wilson disease COLUMN B Porcelain gallbladder Mutation ATP7B gene Bile duct adenocarcinoma 1. Cholangiocarcinoma- Bile duct adenocarcinoma 2. Chronic Cholecystitis- Porcelain gallbladder 3. Wilson disease- Mutation ATP7B gene -Bile duct adenocarcinoma is also called cholangiocarcinoma -CHRONIC CHOLECYSTITIS - In rare instances, there is extensive dystrophic calcification of the gallbladder wall (porcelain gallbladder). -Mutation ATP7B gene - Copper excretion
COLUMN A Alcoholic hepatitis Chronic congestion liver Chronic HBV infection COLUMN B Mallory-Denk bodies Ground-glass hepatocyte Centrilobular necrosis Alcoholic hepatitis - Mallory-Denk bodies Chronic congestion liver - Centrilobular necrosis Chronic HBV infection - Ground-glass hepatocyte -ALCOHOLIC HEPA - Mallory body formation (eosinophilic clumps of intermediate filaments) -In chronic passive hepatic congestion, the centrilobular regions are grossly redbrown and slightly depressed (because of cell death)
COLUMN A Hereditary hemochromatosis a1-antitrypsin deficiency Criggler-Najjar syndrome Dubin-Johnson syndrome- J COLUMN B Protein misfolding, impaired secretion Decreased UGT1A1 activity Mutation MRP2 gene Mutation hepcidin Hereditary hemochromatosis - Mutation hepcidin a1-antitrypsin deficiency - Protein misfolding, impaired secretion Criggler-Najjar syndrome - Decreased UGT1A1 activity Dubin-Johnson syndrome - Mutation MRP2 gene HH -Mutations of genes encoding HFE, transferrin receptor 2 (TfR2), or hepcidin -Mutations of genes encoding HJV (hemojuvelin: juvenile hemochromatosis) Genetic deficiency of UGT1A1 act. (Crigler-Najjar types I and II, some cases Gilbert syndrome)
Created by: matiNIK
 

 



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