Liver diseases Flashcards
Sources of ALP
liver, bone, intestine, kidney and placenta
Elevated LFTs - causes of hepatocellular injury
Viral (A/B/C/D/E/CMV/EBV/HSV/VZV), AI, drugs/toxins, NAFLD, Vascular, Hereditary (A1AT, Wilson’s, celiac, hemochrom.)
Causes of intrahepatic cholestasis
Sex hormones, erthromycin, sepsis, post-op, PBC
Cause of elevated liver ALP
HCC, Mets, Lymphoma; TB, sarcoidosis, histoplasmosis;amoebic/bacterial;medications/idiopathic
Hepatocellular pattern >2x/ULN
Lifestyle mod, + repeat in 6 mo, screen for CLD causes, if still elevated >2xULN, consider liver bx, otherwise observe.
Cholestatic pattern
RUQ U/S, AMA -> if either positive, liver biopsy; if both negative but ALP >1.5x ULN consider Bx, if observe
PBC genetic associations
X monosomy, variants in IL12alpha, IL12 receptor genes
PBC work up
AMA Ab, IgM, Bili, ALP, cholesterol, liver biopsy if AMA negative, (or ANA+SM AB = AMA)
PBC treatment
Ursodeoxycholic acid 15mg/kg/d
Benefits of Urso in PBC
Inc. survival, dec. histologic change and complications (varices)
Refractory PBC on urso
Colchicine, MTX, budesonide
Pruritus treatment in PBC
Cholestyramine give 2-4 hrs after urso, if refractory naltrexone, rifampin
Vitamin deficiencies in PBC
Fat soluble vitamins, screen and Rx osteoporosis even if not Vit D deficient
PSC work up
MRCP +/- ERCP show multifocal beaded bile duct strictures
Liver biopsy features of PSC
Onion skin fibrosis around bile ducts, may exclude diagnosis of autoimmune sclerosing cholangitis