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Answer
ab pain, ascites, hepatomegaly from obstruct of two or more major hepatic veins d/t thrombosis--> encephalopathy. Red-purple liver w tense capsule   Budd-Chiari  
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accumulate unconj bilirubin in brain->kernicterus   Erythroblastosis fetalis  
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Bridging fibrosis septa linking portal tracts, Parenchymal nodules of hepatocytes encircled by fibrosis, Disruption of entire liver architecture. Death of hepatocytes, deposit ECM, vasc reorganization   Cirrhosis  
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chronic CONJUGATED hyperbilirubinemia d/t defect in hepatocell excrete of bilirubin glucuronides across canalicular membrane by multidrug resistance prot 2. liver is Black   Dubin-Johnson synd  
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circular defective ssRNA Deltaviridae. Dependent on HBV. Only makes delta antigen (HDAg)   Hep D  
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extrahepat bile duct obstruct=biliary atresia, gallstones, stricture, panc CA. Pruritus, jaundice, dark urine, light stools, hepatosplenomegaly. Conjug hyperbilirubinemia, increase serum ALP, bile acids, cholest. Yellow-green liver, fibrous jigsaw septa   Secondary biliary cirrhosis  
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hepatocyte ballooning, lobular inflam, steatosis. Fat people. Elevated AST and ALT, AST/ALT ratio less than 1 (above 2 in alcoholic steatohep).   nonalcoholic steatohep (NASH)  
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Baby w prolonged conj hyperbilirubinemia. mostly caused by biliary atresia. jaundice, dark urine, light stools, hepatomega   Neonatal cholestasis  
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mutant ATP7Bimpaired copper excretion into bile and fail to incorporate Cu into ceruloplasmin. Cu build up in liver (chronic hep), brain (putamen atrophy), eye (Kayser-Fleischer rings).   Wilson disease  
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nothing to inhibit destructive proteasesemphysema and liver disease. PiS and PiZ (PiZZ is most common dysfnx). Round to oval cytoplasmic globular inclusions in hepatocytes   Alpha1-Antitrypsin def  
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partially dsDNA. Most recover from acute hep, some get fulminant hep, more get chronic hep (ground-glass hepatocytes), most are healthy carrier, some cirrhosis->hepatocell CA, less recover. Unprotect sex and IV drug use. Detect HBsAg or antibods to HBcAg   Hep B  
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ssRNA. Most common chronic blood infx/cause of liver disease. Most progress to chronic hep (20% cirrhose) (Fatty change of hepatocytes). Unprotect sex and IV drug. Lots of variability (quasispecies), no vaccine. Episodic elevate serum aminotransferases   Hep C  
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ssRNA Hepevirus. water-borne, zoonotic. High mortality when pregnant   Hep E  
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ssRNA Picornavirus, doesn’t cause chronic hep. IgM antibody then IgG antibody for years.   Hep A  
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UGT1A1 completely absent->very high unconj bilirubin->jaundice/icterus   Crigler-Najjar type 1  
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UGT1A1 greatly reduced->form monoglucuronidated bilirubin->extraordiarily yellow skin   Crigler-Najar type 2  
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UGT1A1 reduced a little, no big deal   Gilbert Syndrome  
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viable hepatocytes unable to function properly (tetracycline tox and acute fatty liver of pregnancy (AFLP))   Hep dysfnx o Jaundice, hypoalbuminemia->periph edema, hyperammonemia->hepat encephalopathy, fetor hepaticus = “musty” or “sweet and sour” body odor from mercaptans, hyperestrogenemia->palmar erythema and spider angiomas and hypogonadism and gynecomast  
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young women on birth control. Benign. HNF1alpha and Beta-catenin. Pale biley   Hepatic Adenoma  
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most common liver tumor of kids. Activates WNT/beta-catenin. Beckwith-Weidmann   Hepatoblastoma  
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most common cause of hepat fail, cirrhosis   Chronic Hep fail  
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most common cause of chronic liver disease in US.   Nonalcoholic Fatty Liver (NAFLD)  
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most common benign liver tumors. Red-blue soft nodules   Cavernous hemangiomas  
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maternal HTN, proteinuria, peripheral edema, coag abnorm, DIC. Plus hyper-reflex and convulsions = eclampsia. o HELLP synd = Hemolysis, Elevated Liver enzymes, Low Platelets.   Preeclampsia  
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massive hepatic necrosis w encephalopathy caused most often by drugs (acetomenophin), also Hep A and B   Acute Hep failure  
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malignancy of biliary tree. Most are extrahepatic (perihilar Klatskin tumors). Firm gray w/in bile duct walls. Malignant adenocarcinoma. IL6 overexpress->AKT and anti-apoptotic prot MCL1 active.   Cholangiocarcionoma  
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inflamm and obliterative fibrosis of intrahepat and extrahepat bile ducts. Associated w IBD. Atypical p-ANCAs, hypergammaglobulinemia. Men. Onion-skin fibrosis And another thing: - Nutmeg liver w left sided heart fail or shock   Primary Sclerosing Cholangitis (PSC)  
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most common primary liver cancer. Lots of things lead to it (hepatitis, cirrhosis). Malignant   Hepatocell Carcinoma (HCC)  
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most common biliary tract anomaly creates Phrygian cap   Folded Fundus  
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