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54 Cards in this Set
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- Back
- 3rd side (hint)
What forms the Ampulla of Vater?
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Where biliary tree system dumps into Duodenum. Common Bile Duct and Main Pacreatic Duct
What is Sphincter of Oddi |
Sheath of Smooth mm fibers surrounding the intra-duodenal segment of CBD and Ampulla, constricts to control bile and pancreatic secretions ino the duodenum
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What serum Bilirubin Level indicates Jaudice? What are 3 types of Jaundice?
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Bilirubin > 2.5-3.0 mg/dL
-Prehepatic: hemolysis, large hematomas -Hepatic: Many Dzz -Posthepatic: Gallstones with Obst. Cx of Biliary Tract, Cholangitises |
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What is increased if PRe-hepatic jaundice?
What if Hepatic Jaundice |
Unconjugated Bilirubin on Albumin
Hepatic: since liver conjugates the Unconjugated--with liver problem, both Serum Conjugated and Unconjugated will be elevated. What if post hepatic |
Conjugated Bilirubin will be higher.
and if it can't get into feces it will go to Urine OR Skin |
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When conjugated bilirubin can't get into feces or urine, but rather to skin, why does it itch
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Bile Salts and Acids itch
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How are liver enzymes in Prehepatic J?
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normal
In Hepatic J? |
AST and ALT will be elevated
maybe Alk Phos -with increased levels of Conjugated and Unconjugated |
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How are liver enzymes in Post-hepatic J?
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Elevation of Liver Enzymes
-Increased Alk Phos--Greatly |
so if inc Alk phos think stone or post hepatic J.
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What is Cholelithiasis?
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Gallstones
-20million Ami s have it, most are ASx What is main role of GB |
Absorb excess water/electors, concentrae bile
-Secretes H+ and Mucin --If Gallbladder stasis occurs, risk for lithogenesis |
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The following are risk factors for what?
Prolonged TPNut Pregger Oral Contra Obesity DM |
Cholelithiasis
-Stones Think of 6 Fs |
Female, Fat, Fertile, Forty, Flatulent, Fair Skinned
= cholelithiasis |
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What is Clnical Presentation of Cholelithiasis?
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Biliary Colic (wave like build and decrease in pain)
-in RUQ in 1/3 Pts --due to slow contraction, but stopped, so it contracts harder What precipitates colic |
Meal
-may last up to 3 hours -Vomiting and Diaphoresis are common |
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What if Biliary "coli" pain rises steeply and lasts MORE than 6 hours indicates what?
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Cholecystitis
What is this? |
Obstruciton of cystic duct by gallstones with resultant acute inflammation of the GB
--90% assc w/ stone -may have bacteria, but its usually secondary cause |
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What positive sign will you have with Cholecystitis?
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Murphey's Sign
--Take Deep Breath in, you push in and they ARREST their breathing --Why can cholecystitis have jaundice even w/o stone? |
Also will have Jaundice, with or with out stone. B/c with cystitis, WALL is thickened, so even without a stone you can have blockage
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Tx for Cholecystitis?
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ASx is elective Cholecystectomy
What if calcified or "porcelain" GB? |
Increased risk for Malignancy
--should undergo cholecystectomy |
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What is diff btw Choledocholethiasis and Cholelithiasis
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Choledochel is stone obst Common Bile Duct. Lithiasis is just presence of stones.
What is Tx for Choledochalithiais> |
Cholecystectomy
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What are other Tx options of Cholecystitis?
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Ectomy--laparascopic/lapartomy
- -Chemical Dissolution ERCP with SPhincterotomy -Lithotripsy |
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What is Cholangitis
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Infection of Common Bile Duct?
Common Agents? |
E. Coli (gram-)
Enterococcus (gram+) |
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What is Triad of Sx for Cholangitis
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Charcot's Triad
-RUQ Pain -Fever -Jaundice |
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With continued thickening of bile duct, what results
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Fibrosis
so Sclerosing Cholangitis --can get in UC too (50-75% have it) Who is mostly effected? |
Mostly Young Men
may have elevated Alk Phos Jaundice or Enlarged liver --note: SC is rare--has primary cause assc/ IBD (UC), and Secondary Cause assc/ Surgery/Trauma/Chronic Panc. |
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How is it Diagnosed?
What is Sclerosing Cholangitis linked to? |
SC diagn by ERCP/
inc risk of Cholangiocarcinoma Tx for Sclerosing Cholangitis? |
If Pruritus --bile acid binding agents
or Tx viatmin deficiencys |
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This has non-specific presentation of Jaundice, Hepatomegaly and Pain. Is a cancer?
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Gall Bladder Carcinoma
--Risks are what? |
Galls tone disease, longe term
-Porcelain GB Parasites in asia |
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What are some causes of LIVER Jaundice?
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Toxins/Drugs
Infections Chronic Liver Dzz secondary to ETOH |
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With Hep A, transmission Fecal/Oral
-replication limited to liver, describe seromarkers IgM and IgG |
IgM during 1st 6-12 months
IgG develops after acute illness and remains detectable indefinitely |
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With Hep B, transmission percutaneous/body fluids.
Describe Sero markers |
HBsAg: present early on in process-precedes elevation of LFTs/Bilirubin. Becomes undetecable in 2 months FOllowing onset of jaundice in uncomplicated dz.
What about HBeAg? |
HBeAG appears shortly after HBsAg
--appearance coincides with high degree of viral replication and reflects infectivity --Anit-Hbe signals reduced infectivity |
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When is HBcAg detectable?
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--HBcAg (core) is NOT detectable in Serum?
However, IgM to HBcAg (a-HBcAg-AB) appears early IgG to HBcAg appears later and persists What is the "protective antibody |
--Anti-HBsAg- is Protective antibody--appears late in dz.
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What persists indef in Pts recovered from Hep B
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IgG Anti-HBsurface
IgG Anti-HBcore will stay |
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What is formerly known as NANB Hep?
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Hep C--blood borne--incubation 7 weeks
=Can progress to chronic hepatitis--liver failure/transplant What are the Sero markers? WHen do they appear? |
Anti-HCV --- 30-90 days post
HCV RNA : PCR eval Use Hep C RIBA to comfirm |
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What Hep is the delta ? What is required?
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Hep D -- requires coinfection with Hep B (blood/blood products) or Can SuperInfect someone who already has Hep B
What are Sero Markers |
HDV detectable in serum and liver cells
Anti-HDV: IgM and IgG |
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What Hep is Waterborne, and identified in Asia, India, Africa and Central America?
Transmission? |
Hep E
-Enteric Transmision -- incubation is 5-6weeks Which other Hep does it Resemble? |
Hep E resembles Hep A
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Presentation of Viral hep
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Anorexia, N&V
Fatigue, Malaise Arthralgias, Myalgias, headach Photophobia, pharyngitis, cough low fever What happens when jaundice develops? |
Prodromal Sx usually abate
-Liver becomes enlarged and tender |
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What liver functions change in Viral Hepatitis:
AST/ALT Enias? PT? |
Serum AST/ALT range from 400-4000
-Neutropenia/Lymphopenia are t -PT level elevation |
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What distinguishes a Patient that HAS had the Virus vs someone with Vaccine?
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Past infection will have Anti-HBc AB
vac will not Vac will have Anti-HBs AB |
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With Acute HBV, highly infectious, what will the status be fore the following (ie, + or -, or G or M Ig etc)
HBsAg? HBeAg? Anti-HBe? Anti-HBc? |
With Acute HBV, highly infectious, what will the status be fore the following (ie, + or -, or G or M Ig etc)
HBsAg: + (presents early, gone 2mo post jaundice) HBeAg: + (appears shortly after surface Ag) Anti-HBe: NEG (when Pos= REDUCED Infectivity) Anti-HBc: IgM (appx 6wks after infection) |
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CHRONIC HBV, HIGHLY Infectious
HBsAg? HBeAg? Anti-HBe? Anti-HBc? |
HBsAg: +
HBeAg: + Anti-HBe: Pos (should be Neg I believe?) Anti-HBc: IgG For Late Acute or Chronic with LOW Infectivity? HBsAg? HBeAg? Anti-HBe? Anti-HBc? |
HBsAg: +
HBeAg: NEG Anti-HBe: + (makes sense, positive when LOW infectivity) Anti-HBc: IgG |
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Recovery of Hepatitis B
HBsAg? HBeAg? Anti-HBcore? Anti-HBsurface? |
Recovery of Hepatitis B
HBsAg: Neg HBeAg: Neg Anti-HBcore: Pos IgG Anti-HBsurface: Pos Remote past Infection? |
HBsAg: -
HBeAg: - Anti-HBcore: + IgG Anti-HBsurface: + |
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If Hep B Vaccine:
HBsAg? HBeAg? Anti-HBcore? Anti-HBsurface? |
HBsAg: -
HBeAg: - Anti-HBcore: - Anti-HBsurface: + (protective Ab) |
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Prognosis for Hep A and Hep B
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HAV: majority will recover w/o sequelae
HBV: 95% of adults recover, 95% of Neonates develop CHRONIC Infection What about Hep C |
Chronic Active for HCV
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Tx for Acute Viral Hep?
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Supportive care for 1st 6 months. Then recheck all blood work
--If still HBV, they will prolly have chronic active hepatitis. What are some elements of supportive care |
Restricted physical activity
High C diet Anti emetics, anti-pruritics if bil salt itch |
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Moving on to What?
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Jaundice II Lecture
ETOH Hepatitis Pts have |
Spider angiomas, ascites, edema, bleeding and encephalopathy
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What are keys labs to distinguish ETOH from Viral hepatitis
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Elevated AST/ALT ration > 2 in ETOH
--AST will be 2x ALT others: leukocytosis, thrombocytopenia (direct toxic effect on BM) -elevated bilirubin Elevated prothrombin time reduced serum albumin Mnemonic for ETOH Liver Enzymes? |
AlkoholikerSipsTrinken /ALT ration >2
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Tx for ETOH Hep?
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Vitamen Supplement
thiamine and Vit K What is most common cause of Cirrhosis of Liver |
Alcohol
-10-15% of Alkys develop cirrhosis --Women develop it earlier and with less abuse |
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What is important precursor fro Cirrhosis
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Alcoholic Fatty Liver Dz
--CAN be reveresed |
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What is Prognosis of Cirrhotics if Pt continues to drink
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5 year mortality for 50% with cont ETOH
What is typical COD? |
Hepatic Coma due to buildup of ammonia and go into encephalopathy
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Tx for Cirrhosis
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Supportive care:
Low Protein Diet, Multivits, Abstinence Avoid hepatotoxins |
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What Auto recessive dz affects liver with abnormally liver excretion of Copper?
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Wilsons
What is deficiency in |
Ceruloplasmin
-Clinical manifestations of copper ecess are REARE before 6 years |
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Clinical Presentation of Wilsons?
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50% present with Liver Dz
--Acute Hepatitis Fulminant Hepatitis Chronic Hepatitis cirrhosis Whats wrong if hemolysis occurs? |
Necrosis of hepatocytes likely
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What are the Extrahepatic Sx f Wilson's Dz
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Neurologic or Psychiatric Sx
--w/ Kayser Fleischer Rings -Resting or mvmt dzo -spastcity, rigidity, dysphagia or dysarthria In women? |
Amenorrhea with Wilsons
+ Spontaneous Abortions |
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Pathogensis of Wilson's
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Reduced Ceruloplasmin (long arm of Chrom 13) causes Free Copper in Unbound Form = Toxic
-leads to necrosis, inflammation, fibrosis, cirrhosis in liver If death, what is COD? |
Death from CNS effects or Hepatic Failure
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When is Diagnosis of Wilson's Considered?
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Consider in any Pt < 40 (not younger than 6yrs likely) with:
Unexplained Neuro Synd. Sx of hepatitis, chronic active hep, unexplained LFT abnormals -Hemolytic Anemia with Hep -Unexplained Cirrhosis -Relative with Wilsons |
Note:
With Tx, all manifestations can be prevented Penacillamine |
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How is Wilsons diagnosis confirmed?
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Low Serum Ceruloplasmin in Patient with Kayser Fleischer Rings
OR? |
Low Serum Ceruloplasmin in a patient with elevated hepatic liver [Cu]
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Tx of Wilsons?
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Remove Detoxifying Deposits of Cu
-Penicillamine --Lifelong Therapy recd May need Transplant |
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What dz has chronic comlications of cirrhosis, DM, Arthritis, Cardiomyopathy, Hypogonadotropic hypogonadism
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Hemochromatosis
--Inherited or Acquired (thalassemia or siderblastic anemia) |
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What is Diagnosis for Hemochromatosis?
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Hepatomegally
Skin Pigment DM + heart Dz --Liver Biopsy + Elevated [Iron] |
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Tx for hemochrom?
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Removal of excess body iron
-1-2x weekly Phlebotomy ---usually required for 2-3 years What is Chelation Tx? |
Deferoxamine
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Moving on to Cases:
Case1: Fevers, chills, N&V, Myalgias, Belly Pain Indicates? |
Something Viral
--+ Low Grade Fever, Scleral Icterus (jaundiced) -Mild tenderness in Epigastric--Tender Hepatomegally (15cm, norma is 6-12 cm) Bilirubin 10.8, Direct/conjugated is 4.2 --indicates Hepatic or Posthepatic --AST/ALT Elevated Alk Phos-mildly elevated |
Hepatic jaundice--(Post Hepatic Jaundice would have Much Higher Alk Phos)
--Since its Hepatic, check Hep Panels |
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NOTE: end of lecture notes
BUT CASEs with ANswers at end of Jaundice II LEcter |
Start with PAM THomas
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