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54 Cards in this Set

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What forms the Ampulla of Vater?
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
What serum Bilirubin Level indicates Jaudice? What are 3 types of Jaundice?
Bilirubin > 2.5-3.0 mg/dL

-Prehepatic: hemolysis, large hematomas
-Hepatic: Many Dzz
-Posthepatic: Gallstones with Obst. Cx of Biliary Tract, Cholangitises
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
When conjugated bilirubin can't get into feces or urine, but rather to skin, why does it itch
Bile Salts and Acids itch
How are liver enzymes in Prehepatic J?
normal

In Hepatic J?
AST and ALT will be elevated
maybe Alk Phos

-with increased levels of Conjugated and Unconjugated
How are liver enzymes in Post-hepatic J?
Elevation of Liver Enzymes
-Increased Alk Phos--Greatly
so if inc Alk phos think stone or post hepatic J.
What is Cholelithiasis?
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
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
What is Clnical Presentation of Cholelithiasis?
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
What if Biliary "coli" pain rises steeply and lasts MORE than 6 hours indicates what?
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
What positive sign will you have with Cholecystitis?
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
Tx for Cholecystitis?
ASx is elective Cholecystectomy

What if calcified or "porcelain" GB?
Increased risk for Malignancy
--should undergo cholecystectomy
What is diff btw Choledocholethiasis and Cholelithiasis
Choledochel is stone obst Common Bile Duct. Lithiasis is just presence of stones.

What is Tx for Choledochalithiais>
Cholecystectomy
What are other Tx options of Cholecystitis?
Ectomy--laparascopic/lapartomy
-
-Chemical Dissolution
ERCP with SPhincterotomy
-Lithotripsy
What is Cholangitis
Infection of Common Bile Duct?

Common Agents?
E. Coli (gram-)
Enterococcus (gram+)
What is Triad of Sx for Cholangitis
Charcot's Triad
-RUQ Pain
-Fever
-Jaundice
With continued thickening of bile duct, what results
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.
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
This has non-specific presentation of Jaundice, Hepatomegaly and Pain. Is a cancer?
Gall Bladder Carcinoma
--Risks are what?
Galls tone disease, longe term
-Porcelain GB
Parasites in asia
What are some causes of LIVER Jaundice?
Toxins/Drugs
Infections
Chronic Liver Dzz secondary to ETOH
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
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
When is HBcAg detectable?
--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.
What persists indef in Pts recovered from Hep B
IgG Anti-HBsurface
IgG Anti-HBcore
will stay
What is formerly known as NANB Hep?
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
What Hep is the delta ? What is required?
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
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
Presentation of Viral hep
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
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
What distinguishes a Patient that HAS had the Virus vs someone with Vaccine?
Past infection will have Anti-HBc AB

vac will not
Vac will have Anti-HBs AB
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)
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
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: +
If Hep B Vaccine:
HBsAg?
HBeAg?
Anti-HBcore?
Anti-HBsurface?
HBsAg: -
HBeAg: -
Anti-HBcore: -
Anti-HBsurface: + (protective Ab)
Prognosis for Hep A and Hep B
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
-
Tx for Acute Viral Hep?
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
Moving on to What?
Jaundice II Lecture

ETOH Hepatitis
Pts have
Spider angiomas, ascites, edema, bleeding and encephalopathy
What are keys labs to distinguish ETOH from Viral hepatitis
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
Tx for ETOH Hep?
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
What is important precursor fro Cirrhosis
Alcoholic Fatty Liver Dz
--CAN be reveresed
What is Prognosis of Cirrhotics if Pt continues to drink
5 year mortality for 50% with cont ETOH

What is typical COD?
Hepatic Coma due to buildup of ammonia and go into encephalopathy
Tx for Cirrhosis
Supportive care:
Low Protein Diet, Multivits, Abstinence
Avoid hepatotoxins
What Auto recessive dz affects liver with abnormally liver excretion of Copper?
Wilsons

What is deficiency in
Ceruloplasmin
-Clinical manifestations of copper ecess are REARE before 6 years
Clinical Presentation of Wilsons?
50% present with Liver Dz
--Acute Hepatitis
Fulminant Hepatitis
Chronic Hepatitis
cirrhosis

Whats wrong if hemolysis occurs?
Necrosis of hepatocytes likely
What are the Extrahepatic Sx f Wilson's Dz
Neurologic or Psychiatric Sx
--w/ Kayser Fleischer Rings
-Resting or mvmt dzo
-spastcity, rigidity, dysphagia or dysarthria

In women?
Amenorrhea with Wilsons
+ Spontaneous Abortions
Pathogensis of Wilson's
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
When is Diagnosis of Wilson's Considered?
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
How is Wilsons diagnosis confirmed?
Low Serum Ceruloplasmin in Patient with Kayser Fleischer Rings

OR?
Low Serum Ceruloplasmin in a patient with elevated hepatic liver [Cu]
Tx of Wilsons?
Remove Detoxifying Deposits of Cu
-Penicillamine
--Lifelong Therapy recd
May need Transplant
What dz has chronic comlications of cirrhosis, DM, Arthritis, Cardiomyopathy, Hypogonadotropic hypogonadism
Hemochromatosis
--Inherited or Acquired (thalassemia or siderblastic anemia)
What is Diagnosis for Hemochromatosis?
Hepatomegally
Skin Pigment
DM + heart Dz
--Liver Biopsy + Elevated [Iron]
Tx for hemochrom?
Removal of excess body iron
-1-2x weekly Phlebotomy
---usually required for 2-3 years

What is Chelation Tx?
Deferoxamine
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
NOTE: end of lecture notes
BUT
CASEs with ANswers at end of Jaundice II LEcter
Start with PAM THomas