4 Medicine Hepato Biliary System

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Liver Diseases

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  • HEPATO-BILIARY

    SYSTEM DR.SRINATH.CHANDRAMANI

  • ANATOMY

    PHYSIOLOGY

    SYMPTOMATOLOGY

    INVESTIGATIONS

    INDIVIDUAL DISEASES

    HEPATOBILIARY SYSTEM

  • INDIVIDUAL DISEASES

    VIRAL HEPATITIS

    AUTOIMMUNE HEPATITIS

    DRUG INDUCED HEPATITIS

    ALCOHOLIC HEPATITIS

    CIRRHOSIS + COMPLICATIONS

    LIVER TRANSPLANTATION

    GALLSTONES + PANCRAETITIS

  • Anatomy The right and the Left lobe are independent with regard to :

    1. Portal blood supply

    2. Arterial blood supply

    3. Bile drainage.

    Basic liver architecture :

    Hepatocytes, which constitute two-thirds of the mass of the

    liver.

    Kupffer cells (members of the reticuloendothelial system),

    Stellate (Ito or fat-storing) cells,

    endothelial cells and blood vessels,

    bile ductular cells, and

    supporting structures.

  • Functional classification Based on drainage by major hepatic vein, Liver is

    Functionally divided into 4 Sectors / 8 Segments

    Caudate lobe is anatomically distinct having no

    drainage by either of the 3 major hepatic veins. By

    segment classification, It is classified as Segment 1.

    Significance of above classification :

    Interpretation of Radiological data

    Planning of liver resection procedures.

  • PHYSIOLOGY Organ with a high metabolic rate and rich blood supply.

    Dual Blood supply :

    1. Hepatic artery 20% supply - Oxygen rich

    2. Portal Vein - 80% supply - Nutrition rich

    Portal Zones :

    Blood flows from zone 1 to zone 3 of the acinus and drains

    into the hepatic veins (central veins).

    Secreted bile flows in the opposite direction, in a counter

    current pattern from zone 2 to zone 1.

    The sinusoids are lined by unique endothelial cells that have

    prominent fenestrae of variable size, allowing the free flow

    of plasma but not cellular elements.

    The plasma is thus in direct contact with hepatocytes in the

    subendothelial space of Disse.

  • Functions Hepatocytes perform numerous and vital roles in maintaining

    homeostasis and health. These include :

    synthesis of most essential serum proteins viz. albumin, carrier

    proteins, coagulation factors, many hormonal and growth

    factors.

    production of bile and its carriers (bile acids, cholesterol,

    lecithin, phospholipids),

    regulation of nutrients (glucose, glycogen, lipids, cholesterol,

    amino acids),

    metabolism and conjugation of lipophilic compounds (bilirubin, anions, cations, drugs) for excretion in the bile or

    urine.

  • Symptomatology

    Jaundice

    Parotid enlargement

    Fetor hepaticus

    Spider naevi

    Gynaecomastia

    Abdominal pain

    Ascitis

    Caput medusa

    Dupeytrens contracture

    Paper money skin

    Pruritis

    Testicular atrophy

    High coloured urine

    Pedal edema

    Altered

    sensorium/convulsion

    Peticheia/ echymosis

  • Etiology & Approach Acute ( < 6 months ) Chronic ( > 6 months )

    Infective Infective

    Trauma Toxin/Drug induced

    Vascular Genetic/enzyme deficiency

    Toxin/Drug induced Glycogen storage disorders

    Autoimmune Neoplasms

    Physical obstruction Obstruction

    Recurrent Jaundice

    Hemolysis

    Intermittent obstruction

    Autoimmune hepatitis

    Drug induced hepatitis

    BRIC benign recurrent intrahepatic cholestasis

  • Liver Function Test

    S.Bilurubin

    Transaminases AST / ALT

    Alkaline phosphatase / GGTP

    S.Proteins / A:G ratio

    Prothrombin time

    Alpha-fetoprotein

  • TEST 1 1. Nucleotidase activity is increased in

    (A) Bone disease

    (B) Prostate cancer

    (C) Chronic renal failure

    (D) Cholestatic disorders

    2. Which does not contribute to serum alkaline

    phosphatase

    (A) Liver

    (B) Osteoblasts

    (C) Renal tubular cells

    (D) Neutrophils

    3. Ratio of AST/ALT>1 present in

    (A) Non-alcoholic steatohepatitis

    (B) Alcoholic hepatitis

    (C) Wilson's disease

    (D) All of the above

  • TEST 1

    4. A 50 year old lady presented with history of pain upper abdomen, nausea and decreased appetite for 5 days. She had undergone cholecystectomy 2 year ago. Her bilirubin was 10 mg/dl, SGOT 900 IU SGPT 700 IU/I and serum alkaline phosphatase was 280 IU/I. What is the most likely

    diagnosis?

    (A) Acute pancreatitis

    (B) Acute cholangitis

    (C) Acute viral hepatitis

    (D) Posterior penetration of peptic ulcer

    5. Patients with coagulation abnormality due To liver disease Are likely to have

    (A) Prolonged bleeding time

    (B) Prolonged prothrombin time

    (C) Thrombocytosis

    (D) Short partial thromboplastin time

    6. All are haemoglobin except

    (A) Bilirubin (B) Biliverdin

    (C) Hemosiderin (D) Lipofuscin

    7. Chances of developing kernicterus appears to be significant when serum level of

    unconjugated bilirubin reaches

    (A) 50 mg% (B) 20 mg%

    (C) 10 mg% (D) 5 mg%

  • TEST 1 8. Gilbert's syndrome all are true, except

    (A) Conjugated hyperbilirubinemia

    (B) Fasting hypoglycaemia

    (C) Normal liver histology

    (D) Liver enzymes normal

    9. Conjugated hyperbilirubinemia is seen in

    (A) Gilberts syndrome

    (B) Criggler Najjar type-I

    (C) Criggler Najjar type-II

    (D) Dubin Johnsons syndrome

    10. The test used to diagnose Dubin Johnson syndrome is

    (A) Serum transminases

    (B) Bromsulphalein test (BSP)

    (C) Hippurate test peptidase

    (D) Gamma glutamyl transferase level

  • Viral Hepatitis Hepatotrophic virus.

    Classification based on Route of

    transmission.

    Clinical Features :

    - Prodromal phase

    - Clinical phase

    - Recovery phase

    Extraintestinal manifestations.

  • General info All viruses are RNA viruses except Hepatitis B which

    is a DNA virus.

    Pathological injury occurs due to :

    Direct injury

    Immune mediated

    Incubation period :

    Start with B(+D) , C, E and A and substract 10 from

    60 days.

    B(+D) 60 days , C 50 days, E 40 days and A 30 days.

  • General Info

    The typical morphologic lesions of all types of viral hepatitis

    consist of :

    panlobular infiltration with mononuclear cells,

    hepatic cell necrosis,

    hyperplasia of Kupffer cells,

    variable degrees of cholestasis.

    Hepatic cell regeneration is present, as evidenced by

    numerous mitotic figures, Multinucleated cells, and rosetteor pseudoacinar formation.

    Liver cell damage consists of hepatic cell degeneration and

    necrosis, cell dropout, ballooning of cells, and acidophilic

    degeneration of hepatocytes (forming so-called Councilman

    or apoptotic bodies).

    Lipofuschin is a wear and tear pigment.

  • Waterborne Hepatitis

    Parameter Hepatitis A Hepatitis E

    Epidemiology

    Mode of transmission

    Incubation period

    Clinical peculiarity

    Diagnosis

    Treatment

    Prognosis

  • Blood borne Hepatitis Parameter Hepatitis B Hepatits C

    Epidemiology

    Mode of

    transmission

    Mother to child

    Needle stick injury

    Incubation period

    Clinical peculiarity

    Diagnosis

    Treatment

    Prognosis

  • Serum markers for Hepatitis B

    HBsAg

    Anti-HBs antibody

    HBcAg

    Anti- HBcAb

    HBeAg

    Anti Hbe antibody

    HBV DNA by PCR

  • Hepatitis B Plus D

    Co-Infection Superinfection Both together HBV precedes

    HDV infection

    IgM HBc positive IgM HBc negative

    No change in chronicity 6 fold increase in

    chronicity

    No change in cirrhosis Hastened progression

    to cirrhosis

    Increase risk of HCC Greater risk of HCC

  • Autoimmune hepatitis Autoimmune hepatitis is characterised by :

    Female predominance 2nd decade / post menopausal.

    Hyperglobulinemia

    Positive circulating auto anti-bodies

    Association with HLA-DR3 and HLA-DR4.

    Prominence of extrahepatic features of autoimmunity

    Secondary conditions have to be excluded viz.

    virus,drugs,alcohol,etc.

    Good response to immunosuppressive therapy. In general,

    responders have :

    Florid clinical picture

    High antibody titer/ hyper globulinemia

    Higher SGPT

    Active Liver histology.

    Classification is based on circulating antibody type.

    may have a 6-month mortality of as high as 40%.

  • AUTOIMMUNE HEPATITIS

    TYPE 1 TYPE 2 TYPE 3

    ANTIBODY ANA ANTI-LKM ANTI-LsAg

    EPIDEMIOLOG

    Y

    2-3RD DECADE

    F >> M

    4-5TH DECADE

    F>M

    5-6TH DECADE

    M>F

    CLINICAL

    COURSE

    ACUTE,

    FLORID

    CHRONIC,

    INDOLENT

    UNDERLYING

    MALIGNANCY

    TREATMENT IV STEROIDS,

    PLASMAPHERE

    SIS

    ORAL

    STEROIDS

    UNDERLYING

    MALIGNANCY

    PROGNOSIS GOOD MODERATE POOR

  • Drug induced Hepatitis

    Mode of Hepatic Injury

    In general, two major types of chemical hepatotoxicity have been recognized :

    (1) direct toxic type and

    (2) idiosyncratic type.

    Drug induced Hepatitis is classified based on the clinical and labaratory pattern.

  • Patterns of hepatotoxicity Hepatitis

    Anesthetic : Halothane

    Anticonvulsant : Phenytoin, carbamazepine

    Antihypertensive : Methyldopa, captopril, enalapril

    Antibiotic : Isoniazid, rifampin, nitrofurantoin

    Diuretic : Chlorothiazide

    Antidepressant : Iproniazid, amitriptyline, imipramine, trazodone,

    venlafaxine

    Anti-inflammatory : Ibuprofen, indomethacin, diclofenac

    Antifungal : Ketoconazole, fluconazole, itraconazole

    Antiviral : Zidovudine, didanosine, nevirapine

    Calcium channel blocker :Nifedipine, verapamil, diltiazem

    Mixed hepatitis/cholestatic

    Immunosuppressive : Azathioprine

    Lipid lowering : Nicotinic acid, lovastatin and other statins

    Antibiotic : Amoxclav, trimethoprim-sulfamethoxazole

    Antifungal : Terbinafine

  • Patterns of Hepatotoxicity Cholestasis

    Anabolic steroid : Methyl testosterone

    Antibiotic : Erythromycin, nitrofurantoin, rifampin, amoxclav, oxacillin

    Oral contraceptive : Norethynodrel with mestranol

    Anticonvulsant : Carbamazepine

    Calcium channel blocker : Nifedipine, verapamil

    Fatty liver

    Antibiotic : Tetracycline

    Anticonvulsant : Sodium valproate

    Antiarrhythmic : Amiodarone

    Antiviral : NRTI, Protease inhibitors.

    Oncotherapeutic : methotrexate

  • Patterns of hepatotoxicity Toxic (necrosis)

    Hydrocarbon Carbon tetrachloride

    Metal : Yellow phosphorus

    Mushroom : Amanita phalloides

    Analgesic : Acetaminophen

    Granulomas

    Anti-inflammatory : Phenylbutazone

    Antibiotic : Sulfonamides

    Xanthine oxidase inhibitor : Allopurinol

    Antiarrhythmic : Quinidine, diltiazem

    Anticonvulsant : Carbamazepine

    Vascular injury

    Veno-occlusive/Portal vein thrombosis : Cytotoxic / Irradiation

    Sex hormones

    Neoplastic

    Focal adenoma : sex hormones

    Hepatocellular carcinoma : Danazol, Anobolic hormones

  • Management Diagnosis : is mainly based on history. Correlation with clinical

    manifestation and above mentioned clinical picture helps. Anti-Histone Antibody is important marker.

    Treatment : is largely supportive, except in acetaminophen

    hepatotoxicity.

    Withdrawal of the suspected agent is indicated at the first

    sign of an adverse reaction.

    Liver transplantation maybe curative in fulminant cases.

    Glucocorticoids for drug hepatotoxicity with allergic features,

    silibinin for hepatotoxic mushroom poisoning, and

    ursodeoxycholic acid for cholestatic drug hepatotoxicity

    have never been shown to be effective and are not recommended.

  • Misc Hepatitis

    Reyes syndrome

    Characterised by vacuolisation of liver

    and renal tubules.

    Increases Transaminases, Prothrombin

    time and ammonia

    hypoglycaemia and metabolic alkalosis.

    Characterised by lack of jaundice.

  • Misc Hepatitis Budd-Chiari syndrome : Extremely rare disorder.

    Thrombosis of Hepatic vein.

    Etiology : Hypercoagulable states , Malignancy,

    Myeloproliferative state.

    Clinical features depend on extent and rate of

    venous obstruction.

    Hepatomegaly and Ascitis present in nearly 100%.

    Varices in >50%.

    Angiography diagnostic. CT preferred mode. Search

    for underlying cause.

    Medically lifelong anticoagulation . Surgical stenting.

    SOS Liver transplant.

    Prognosis is poor. Death wihin 3 years if untreated.

  • Misc Hepatitis Liver abscesses : Most common Amoeba

    vs Pyogenic.

    Intense RHypochondriac pain,

    septicaemia. Intercostal tenderness.

    USG, FNAC,CT is diagnostic.

    Multiple sites is Pyogenic, Single lesion is

    amoebic.

    Metronidazole for 2 weeks. Antibiotics SOS.

    Drainage SOS.

    Prognosis excellent. Rupture and sub

    phrenic abscess are complication.

  • Summary of chronic hepatitis

    Etiology Age/gender Association Diagnosis

    Hep B & D All/males

    Orient, African,

    Drug users,

    Homosexuals,

    Immunosupressed

    HBsAg,HBVDNA

    HEP C All/equal

    Blood transfusion

    Drug users,

    Hemodialysis

    Anti-HCV Ab

    HCV RNA by PCR

    Autoimmune 14-25 yrs/

    Females

    Multisystem

    involvement

    ANA, ASMA,

    Anti-LKM, LsAg

    Drug induced 3rd-5th decade

    females Drug history

    Anti histone,

    drug levels

    Wilson 10-30 yrs/

    equal

    Family history,

    Hemolysis

    KF ring,biopsy

    Neurological

    symptom.

    Cu,Cerupl. level

  • TEST 2

    11. True about hepatitis A include

    (A) Spreads by faco-oral route

    (B) Incubation period is 45-180 days

    (C) Predisposes to cirrhosis

    (D) lgG anti-HIV antibodied used for diagnosis

    12. The marker of Hepatitis B in the window

    period is

    (A) HBsAG (B) Anti HBsAG

    (C) Anti HBC (D) HBcAg

  • TEST 2 13. Two laboratory technicians from a District hospital were tested

    Australia Antigen positive. True about the further steps is.....

    (A) Discard all the blood samples collected by them.

    (B) Do not allow them to work in the laboratory.

    (C) test the if they are Anti-HBC (IgM) positive

    (D) Retest them for Australia antigen after 6 months

    14. Antigen which does not appear in blood in Hepatitis B is....

    (A) HBc Ag

    (B) HBe Ag

    (C) HBs Ag

    (D) None of the above

    15. Acute liver injury associated with hepatitis B virus is due to

    (A) Direct cytopathic effect of the virus

    (B) Sensitized cytotoxic T-cells

    (C) Immune-complex mediated tissue damage

    (D) Vasculitis

  • TEST 2

    16. Extrahepatic manifestation of Hepatitis-B are

    (A) Aplastic anemia

    (B) Cryoglobulinemia

    (C) Peptic ulcer

    (D) Gallstones

    17. The likelihood of becoming an HbsAg carrier

    after acute HBV infection is high in....

    (A) Neonates

    (B) Chronic hemodialysis patients

    (C) Persons with Down's syndrome

    (D) Persons with HIV infection

    (E) All of the above

  • TEST 2 18. A person screened for blood donation, which of the following

    serology is safe for blood donation?

    (A) Anti HBsAg positive

    (B) HBsAg positive

    (C) Anti HBc positive and anti HBSAg positive

    (D) HBeAg positive

    19. The disease associated with hepatitis C virus is...

    (A) Leprosy (B) Lichen planus

    (C) Psoriasis (D) Vitiligo

    20. Which of the following drugs is known to cause granuloma in the

    liver?

    (A) Allopurinol

    (B) Nifedipine

    (C) Tetracycline

    (D) Methyl testosterone

  • Alcoholic Liver Disease

  • Cirrhosis

    Etiological classification of cirrhosis :

    (1) alcoholic;

    (2) cryptogenic and posthepatitic;

    (3) biliary;

    (4) cardiac; and

    (5) metabolic, inherited, and drug-

    related.

    (6) NAFLD / NASH

  • Biliary Cirrhosis Primary biliary cirrhosis :

    auto- immune

    AMA, Lipoprotein X

    CREST syndrome,

    Ursodeoxycholic acid

    Cholestyramine

    Liver transplant with excellent results.

    Secondary biliary cirrhosis

    Better prognosis

    6-12 months

    surgical correction is the cure.

  • NAFD/NASH/NON-ALCOHOLIC

    CIRRHOSIS

    MORE IN FEMALES

    ASSOCIATION WITH PANCREATIC

    INSUFFICIENCY / DM/OBESITY

    HAS BECOME THE COMMONEST

    CAUSE OF CRYPTOGENIC CIRRHOSIS

  • Complications of Cirrhosis

    Variceal bleeding

    Hepatic Encephalopathy

    Spontaneous Bacterial Peritonitis

    Coagulopathy

    Hepato-renal syndrome

    Hepato-Pulmonary syndrome

    CHILD PUGH Grading of Liver disease

  • PORTAL CIRCULATION

  • Adult portal circulation Portal blood flow : 1000 1200ml/min

    Portal pressure : normally 7mm of Hg.

    Various sites of porto-systemic shunts/collaterals exist in the body.

    Normally 100% of portal venous blood can be recovered from the

    hepatic veins.

    Collateral circulation comes into play in 2 situations :

    1. INTRA HEPATIC PORTAL VEIN OBSTRUCTION :

    The site of obstruction is within the liver. Commonest example being

    cirrhosis.

    Both physical as well as myo-proliferative factors are involved in portal

    vein obstruction.

    In such cases barely 13% blood flows through the hepatic vein, rest is

    shunted.

    Blood ultimately reaches Superior vena cava through the Azygous

    system.

    Typically the collaterals are abdominal shunts as discussed below.

    Few collaterals to pulmonary veins described but rare.

  • 2. EXTRA HEPATIC PORTAL VEIN

    OBSTRUCTION :

    The block lies outside the liver and hence

    collaterals develop to bypass the block

    and enter the liver as close to the porta

    hepatis as possible.

    Lumbar collaterals may be large.

    The volume of shunt may be smaller than

    intra hepatic obstruction.

  • SITES OF PORTO-SYSTEMIC ANASTOMOSIS : (Refer Figure)

    SITE PORTAL VEIN SYSTEMIC VEIN CLINICAL OUTCOME

    1. Cardia Stomach a. Left Gastric Esophageal Gastro-esophageal

    b. Posterior Gastric Diagphramatic & Fundic varices c. Short Gastric Intercostal/Azygous

    2. Anus Sup. Hemorrhoidal Middle & Inferior Rectal varices

    Vein Hemorrhoidal Vein

    3. Falciform ligament Paraumbilical Umbilical circulatn Caput Medusa

    Vein of fetus

    4. Abdominal organ Veins of Sappey Diapragmatic Prominent veins

    Lumbar vein

    5. Renal Splenic vein Left Renal vein Not known

  • Porto-systemic Anastomosis

  • Hepatic Encephalopathy

    Cause

    Precipitating Factors

    Daignosis

    Clinical Grading

    Management

  • Spontaneous Bacterial Peritonitis

    Difference from secondary

    bacterial peritonitis

    Mixed anaerobic flora

    Presentation

    Diagnosis

    Treatment

    Prophylaxis

  • Hepato-renal Syndrome Diagnostic criteria

    S.Creatinine > 1.5 mg/dl / GFR < 40ml/min

    Failure to improve with volume expansion

    Avid Sodium retention < 20mmol

    Hyponatremia

    Rule out Volume loss/Nephrotoxic Drugs

    Anatomically normal kidneys.

    No Hematuria/Proteinuria

    Vasopressin.

    Liver transplant.

  • Hepato-pulmonary syndrome

    Orthodeoxia

    Concept of Pa-aO2 gap.

    Prognosis

  • Orthoptic Liver transplant Indications for liver transplantation are :

    In children Biliary atresia, Neonatal hepatitis, Antitrypsin

    deficiency , Inherited disorders of metabolism, Wilsons disease, Glycogen storage disorders.

    In adults, Primary biliary cirrhosis, Viral hepatitis, drug/toxin

    induced hepatitis and end stage liver disease.

    Contraindications for liver transplantation :

    Absolute : HIV, Malignancy

    Relative : Age > 70, Renal failure, immunosuppression

  • Types of donor organ

    Cadaver donor transplant : demand >>> supply.

    Unpredictable. Hence always done in emergency. Transport issues.

    Can be split into potential 2 (1 adult + 1 child) rarely.

    Living-donor transplantation : can reduce waiting time and cold-ischemia time.

    done under elective, rather than emergency,

    circumstances;

    and may be lifesaving in recipients who cannot afford to

    wait for a cadaver donor.

    Success measured as 1-year survival has improved from_30% to_85% today.

  • Pancreatitis Pancreatitis is the inflammation of the pancreas.

    Phyiology : Pancreas is a exocrine gland as well as an endocrine

    gland.

    Pancreas have a large functional reserve so as to maintain normal

    function till >90% is destroyed. Even sensitive tests (Secretin stimulation)

    detect only when >60% damage has occurred. Moreover the

    symptoms of disease are very vague and non-specific.

    Epidemiology : Pancreatic insufficiency is found in 0.4-5% of autopsy

    studies.

    However true incidence and prevalence is very difficult due to above

    mentioned reasons.

    Incidence increases with age i.e. > 15% have some problem > 65

    years.

    Common in the male gender, however this is changing and closely

    matches alco

  • Pancreatitis is of two types depending on

    the duration viz.

    Acute pancreatitis < 2 weeks

    Chronic pancreatitis > 6 weeks

    more often months

  • Etiology : remember the following acronym:

    A - Alcohol

    Anatomic pancreatic division, Annular pancreas

    Auto-immune Sjogrens syndrome

    B - Bile stones / Gallstones

    Biliary duct strictures

    C - Carcinoma

    Cholestrol - Hypertriglyceridemia

    Connective tissue disorder - TTP

    D - Drugs Anti-HIV , Valproate, Sulfonamides

    E - ERCP

    Others - Post surgery

    Trauma

    Renal failure

    Infections Coxsackie, Mumps

  • Hyperamylasemia

  • Test 3 21. Most common presenting symptom in primary biliary cirrhosis is...

    (A) Jaundice

    (B) Pruritis

    (C)Splenomegaly

    (D)Gastrointestinal bleeding

    22. Which of the following statements are Correct of cirrhosis EXCEPT

    (A) Antimitochondrial antibodies positive in primary biliary cirrhosis.

    (B) In late stage of PSC treatment is liver transplantation.

    (C) In advanced stages major blood supply is through hepatic vein.

    (D) Elevated lipoprotein-X in PBC.

    23. Which one of the following is not a feature of liver histology in non-

    cirrhotic portal fibrosis (NCPF)?

    (A) Fibrosis in and around the portal tracts.

    (B) Thrombosis of the medium and small portal vein branches.

    (C) Non-specific inflammatory cell infiltrates in the portal tracts.

    (D) Bridging fibrosis

  • Test 3 24. A 20 year old boy presented with severe hematemesis. On

    examination there was no hepatomegaly, mild splenomegaly

    present. On endoscopy esophageal varices were

    seen. What is the most probable diagnosis?

    (A) Cirrhosis liver

    (B) Budd Chiari syndrome

    (C) Non cirhotic portal fibrosis

    (D) Veno occlusive disease

    25. Which of the following statements is incorrect with regard to

    heptorenal syndrome in a patient with wlicirrosis?

    (A) The creatinine clearance is > 40 ml/min

    (B) The urinary sodium is less than 10 mol/L

    (C) The urine osmolality is lower than the plasmaosmolality.

    (D) There is poor response to volume expansion.

  • Test 3 27.. All of the following drugs are used in hepatic encephalopathy,

    except....

    (A) Mannitol (B) Metronidazole

    (C) Lactulose (D) Phenoharbitone

    28. Which of the following is false regarding non-alcoholic fatty liver

    (A) Seen in diabetic

    (B) Clofibrate is used in treatment.

    (C)Commonest cause of cryptogenic cirrhosis

    (D) Associated with transaminitis

    29. Reye's syndrome is characterized by all except ....

    (A) Viral infection is seen.

    (B) Present as deep jaundice

    (C) Cerebral edema

    (D) Microvesicular fatty infiltration

  • Test 3 30. What is the line of management of a case of moderate to severe

    hepatic insufficiency with portal hypertension, according to the modified

    Pugh's classification?

    (A) Sclerotherapy

    (B) Orthotopic liver transplantation

    (C) Shunt Surgery

    (D) Conservative

    31. In hereditary spherocytosis, the gall bladder shows....

    (A)Mixed stones

    (B)Cholesterol stones

    (C)Pigment stones

    (D)All of the above

    32. Acalculous cholecystitis can be seen in all the following conditions

    except

    (A) Enteric fever

    (B) Dengue haemorrhagic fever

    (C) Leptospirosis

    (D) Malaria

  • Test 3 33. A patient presents with jaundice, right upper quadrant pain

    chills with high fever, hypotension and mental confusion. The

    most likely diagnosis is...

    (A) Gallstone pancreatitis

    (B) Hepatitis

    (C) Acute suppurative cholangitis

    (D) Amoebic liver abscess

    34. Hemoblia is characterised by all except

    (A) Jaundice (B) Biliary colic

    (C) Malena (D) Fever

    35. Serum amylase usually becomes elevated in acute

    pancreatitis after

    (A) 1/2 hrs. (B) 4-6 hrs.

    (C) 24-48 hrs. (D) 48-72 hrs.

  • Test 3 36. Serum amylase level is raised in all except

    (A) Acute pancreatitis

    (B) Perforation of stomach

    (C) Strangulated small intestine

    (D) Acute appendicitis

    37. Serum amylase is raised in

    (A) Rubella (B) Measles

    (C) Mumps (D) Chicken pox

    38.. The following can be associated with acute pancreatitis

    EXCEPT

    (A) Hyperparathyroidism

    (B) Hyperthyroidism

    (C) Hypercalcemia

    (D) Hypertriglceridemia

  • Test 3 39. Which one of the following types of pancreatitis has the best prognosis?

    (A) Gall stone pancreatitis

    (B) Alcoholic pancreatitis

    (C) Idiopathic pancreatitis

    (D) Traumatic pancreatitis

    40. How much of the acinar pancreas must be destroyed to result in steatorrhoea

    (A) 10% (B) 30%

    (C) 60% (D) 90%