The document provides an overview of the liver, biliary apparatus, and related diseases. It describes the anatomy and blood supply of the liver and gallbladder. It discusses hepatocellular carcinoma and bile duct cancers, including risk factors, clinical presentation, diagnosis, and treatment. Hepatocellular carcinoma is often associated with liver cirrhosis and viral hepatitis. Gallbladder cancer commonly occurs in the setting of gallstones and has a poor prognosis due to late presentation. Bile duct cancer risk factors include liver flukes and primary sclerosing cholangitis. Obstructive jaundice is a common symptom of bile duct cancers.
1. LIVER & BILLARY APPARATUS
Presented by: Dr. Isha Jaiswal
Moderator: Dr. Rohini Khurana
Date: 23 July 2014
2. Liver-Introduction
• Also called ‘hepar’.
• Largest gland in the body.
• 2nd largest gland of the body
• Weighs about 1600 gm in
males,1300 gm in females.
• Occupies the right hypochondrium,
epigastrium & left hypochondrium.
• Most part of the liver is covered by
ribs & costal cartilages.
3. Lobes of Liver
• Liver is divided into right & left lobes by falciform ligament .
• Ligaments
Coronary ligament
Triangular ligament
Ligament of treitz
falciform ligament
5. Peritoneal relations of the Liver
The Lesser omentum
• Encloses the portal triad (bile duct, hepatic artery and portal vein )
• Passes from the liver to lesser curvature of the stomach + 2 cm of duodenum
• Thick free edge -- hepatoduodenal ligament
• Sheet like remainder – hepatogastric ligament
7. Arterial supply is by portal vein &
hepatic artery.
Venous drainage is by hepatic veins
which drain into inferior vena cava.
Blood supply
8. • Nerve Supply
Parasympatheticsupply is by the preganglionicfibers of the vagus nerve.
Sympathetic innervation is by the postganglionic fibers from the coeliac
plexus.
• Lymphatic Drainage
Lymphatics from upper surface drain into nodes in the posterior
mediastinum.
Lymphatics from lower surface drain into hepatic nodes and celiac nodes.
9. Biliary Apparatus :
It collects bile from the liver ,stores in the gallbladder&
transmits to 2nd part of duodenum
• Gall bladder.
• Cystic duct.
• Right and left hepatic ducts which unite to form
Common Hepatic Duct.
• Common Bile duct formed by the union of cystic duct
and common hepatic duct.
10.
11. Gall Bladder
• Pear shaped organ
• Reservoir of bile
• Situated in gb fossa
• Fundus
• Body
• Neck
• Infundibulum
• Cystic duct
Parts of Gall Bladder
12. Calot triangle
The triangle is bounded by the
cystic duct, the common hepatic
duct, and the inferior border of
the liver.
Important structures including:
the cystic artery, the right
hepatic artery, and the cystic
duct lymph node.
13. GALL BLADDER
Blood Supply
• Arterial supply is by cystic artery, a branch of the right hepatic artery.
• Venous drainage is into the portal vein.
Nerve Supply
• Parasympatheticsupply is by pre-ganglionic fibers from the vagus nerve.
• Sympathetic innervation is by post-ganglionic fibers from the coeliac
plexus.
Lymphatic Drainage
• Lymphatics drain into cystic nodes, hepatic nodes and coeliac nodes
22. Percutaneous (through the skin) Transhepatic (through the liver)
Cholangiogram.
In this procedure, a thin needle is inserted through the skin and into the bile
ducts. A dye is injected through the needle so that a contrast image will show
up on X-rays
25. ERCP
This radiograph taken during an ERCP procedure demonstrates the hepatic ducts;
common hepatic duct, cystic duct, and common bile duct are demonstrated. Note
the spiral appearance of the cystic duct due which is the valve of Heister. The
pancreatic ducts and ampulla of Vater are not demonstrated
27. • Hepatocellular cancer is the fifth most
common cancer in the world and the
third most common cause of cancer
mortality
• Male to female:3:1
• Geographical variation: more common
in sub Saharan Africa, South Korea
,China & less in US ,UK
• however the incidence is increasing due
to greater prevalence of HCV infection
28. VIRAL:
with persistent HBV & HCV infection, the risk of HCC
increases by a factor of 100.
CHEMICALS & TOXINS:
Chemical injuryinducedby
• Ethanol,
• aflatoxin
• Fungi: Aspergillus flavus & parasiticus
CHRONIC LIVER DISEASES
• Chirrhosis (70-90%)
• hemochromatosis,
• Wilson's disease,
• hereditary tyrosinemia
RISK FACTORS
30. Hepatocellular carcinoma
• Mean age: 6th -7th decade
• M:F= 3:1
• Prevention: HBV vaccination, disposable syringes, blood
screening, universal precaution of health care worker,
timely treatment of HCV with interferon
• Surveillance: as per AASLD
in high risk pt only
AFP & ultrasonography at 6 month interval
31. • Diagnosed as per AASLD criteria: AFP levels of more than
200ng/ml with a dominant liver nodule more than 2 cm in a
chirrhotic pt on a dynamic imaging technique with typical
enhancement pattern oh HCC
• In general a chronic hepatitis or chirrhotic pt with any
dominant solid nodule that is not clearly a hemangioma
should be considered HCC unless proven otherwise
• Histological diagnosis reserved for pt planned for non
surgical therapy.
• tumor seeding from FNAC & biopsy 1.6-5%
32. Spread of HCC
• Local spread
• Intrahepatic metastasis
• Hematogenous: portal vein & hepatic vein are
invaded in 20-90%of HCC depending on
size(dynamic ct required)
• Lymphatic spread least common
• Lung is the most common site of distant
metastasis
33. Role of AFP
• Valuable diagnostic marker
• Normal value less thn 20 ng/ml
• Tested by radioimmuno assay
• Elevated in 80-90% cases
• Level corelates with tumor size
• May be elevated in chronic hepaptitis and chirrhosis
• Level above 250ng/ml are more sugestive of HCC
• AFP along with CEA used to diffrentiaie HCC from liver
secondaries
• Other tm marker: DCP(des gamma carboxy prothrombin) or PIVKA
(protein induced by vit k def. or antagonist) raised in 91 %)
34. Clinical presentation
• asymptomatic
• Patients with symptoms usually
suffer from chronic hepatitis and
liver cirrhosis.
• Clinical symptoms include
general fatigue, nausea
low grade fever,
poor appetite,
wt. loss,
abdominal distension ,pain
jaundice,
Bleeding manifestations
35. CLINICAL HISTORY
• history of hepatitis, jaundice, blood transfusion, use of intravenous
drugs, or exposure to aflatoxins, alcohol abuse
EXAMINATION
• may reveal clubbing cynosis, jaundice, flapping tremors, skin
pigmentation, anemia
• hepatomegaly splenomegaly, dilated abdominal veins, palmar
erythema, leg oedema, ascitis abdominal bruit
• Paraneoplastic: hypoglycemia, polycythemia ,hypercalcemia
,hypercholestrolemia, carcinoid syndrome,porphyria,etc
38. HCC ON MRI this man was referred for liver
transplantation for a solitary 5 cm liver nodule on cect (yellow)
but mri s/o multiple lesion on delayed images
39.
40. Billiary tract cancer
• They are highly lethal because most are locally advanced at
presentation.
• Gallbladder cancer (m.c) 2/3rd
• bile duct cancer 1/3rd
• surgery is the treatment of choice and is associated with long term
survival For unresectable tumours, the purpose of treatment is to
palliate symptoms such as obstructive jaundice, biliary tract infection,
pain, and ascites.
41. Gall bladder cancer
• it is the fifth most common cancer of the gastrointestinal tract
• Most common billiary tract cancer
• Gallbladder carcinoma is associated with stones in over 90% of patients
• Poor prognosis, highly malignant, rapidly disseminating difficult to
diagnose preop.
• Age: 6 th to 7 th decade
• ratio of females to males is 3:1
• In India high incidence in north and central india less in south
• M.c HPE: adeno ca
• Location:
fundus (60%),
body (30%),
neck (10%)
42. • Disorder of gallbladder:
– Cholelithiasis in 64-98%
• Gallbladder carcinoma occurs in only 1% of all patients with gallstones!
– Porcelaingallbladder(in 4-60%): prophylectic cholecystectomy indicated
– Chronic cholecystitis
– Gallbladderpolyp: a polyp >2 cm is likely malignant!
– Chronic typhoid carriers
• Disorder of bile ducts:
– Primary sclerosing cholangitis
– Congenital biliary anomalies:cystic dilatationof biliary tree, choledochal cyst,
anomalous junction of pancreaticobiliary ducts, low insertion of cystic duct
• Inflammatory bowel disease (predominantly ulcerative colitis, less common in Crohn disease)
• Familialpolyposis coli
• exposure to carcinogens (azotoluene, nitrosamines)
Gallbladder Carcinoma: risk factors
43. SPREAD OF GB CANCER
• Routes of spread:
local invasion: liver seg 4 & 5, duodenum ,transverse colon porta hepatis.
Lymphatic: pericholedochal, cystic, sup pancreaticodudnal, retropancreatic
celiac ,paraaortic L.N
Hematogenous via hepatic and portal veins to liver ,lung
Perineural in wall of gall bladder
Transperitoneal spread to omentum ,peritoneum leading to ascitis
Intraductal spread in papillary varity
44. Clinical features of CA GALLBLADDER
• Asymptomatic at early stage except tm located at
neck of gall bladder
• advanced diseases at presentation
• Early CA GB incidental finding on cholecystectomy
• Clinical features: abd. pain., dyspepsia,
anorexia,nausea vomiting.wt
loss .
jaundice pallor
ascitis
hemetemesis,malena
45. • Diagnosis is by USG and CT
• Dynamic CT angiography is advised if surgery is planned
• ERCP & PTC may be used to evaluate billiary tree if usg does not show site
of billiary obstruction
• Histological diagnosis can be attempted USG guidedbiopsy/FNAC from
liver mets.
• Gb biopsy is usually not advisable in view of billiary peritonitis (5%)
however FNAC can be attempted (88.5% accuracy)
• Radical cholecystectomy is TOC
Cholecystectomy
+resection of liver (wedge & anatomic seg 4 & 5)
+portal lymphadenectomy from hilum of liver, pancreas, duodenum celiac
axis
Invasion of hepatic artery and portal vein are considered criteria of
unresectibility
47. Direct invasion of the liver by gallbladder cancer in a 66-year-old
woman
48. Bile Duct Carcinoma:
Rare tumor and about two third are located at the hepatic duct bifurcation
Very common in endemic areas of developing countries such as northeast
Thailand
Mean age of presentation:60-65 years
M:F=1.3:1
95% are adenocarcinoma
term cholangiocarcinoma describes cancers arising from the
epithelial cells of the bile ducts, which include intrahepatic,
perihilar, and extrahepatic biliary tree.. But is more commonly used
for peripheral intrahepatic tm
Anatomical division:
*intrahepatic ;
*perihilar (Klatskin tumors)
*proximal extrahepatic
*distal extrahepatic
49. 49
Risk factors for bile duct cancer
Hepatolithiasis :2-10%
Choledochal cyst
Polycystic liver
Parasitic infection: Liver fluke: Clonorchis sinensis and Opisthorchis viverinni
Primary sclerosing cholangitis (PSC)
Ulcerative colitis
Biliary cirrhosis
HCV infection
Nitrosamine exposure
PATHOGENESIS: long standing inflammation &
chronic injury to billiary epithelium
50. Bile Duct Cancer
Intrahepatic CCs: develop in the
smaller bile duct branches inside the
liver
Extrahepatic CCs: originate in the bile
duct along the hepato-duodenal
ligament
Hilar CCs: develop at the hilum
Classification of bileduct cancer is important for
undurstanding of pathogenesis, diagnosis, and
management
51. Intrahepatic biliary duct cancers manifest similar as liver cancers with minimal
dilation of billiary radicals &non obstructive jaundice
Extra hepatic biliary cancers (more than 50% in upper 1/3rd) .
Result in Dilation of intra & extra hepatic bile duct till level of obstruction
manifest as obstructive jaundice
for tumors in upper and mid 1/3rd PTC is use
to observe the biliary tree.
In lesion arising in distal 1/3rd or non dilated
intrahepatic radicals ERCP is useful
for diagnosis
52. Spread of bile duct cancer
• Local spread: longitudinally along bile duct or adjacent vascular
structure(hepatic artery ,portal vein) and in liver
• Lymphatic: cystic, pericholedochal. peri pancreatic, celiac ,superior
mesentric nodes.
• Hematogenous spread: mc to liver
53. 53
Sign and Symptom
The most common presenting symptoms of obstruction of the bile
duct
include
painless jaundice,
clay-colored stool,
tea-colored urine,
pruritus.
abdominal pain,
fever,
general malaise,
abdominal distention,
anorexia,
and weight loss
54. Criteria of unresectibility:
extensive b/l intrahepatic spread on cholangiography
Involvement of main trunk or both branches of portal
vein or hepatic artery
Involvement of 1 branch of portal vein with opp branch of
hepatic artery
Combined vascular involvement on 1 side with extensive
cholangiographic involvement on other side
55. Cholangiocarcinoma with IHBRD
Klatskin Tumor: Axial CT of the abdomen with
intravenous contrast reveals an enhancing mass near
the gallbladder neck (yellow arrow). This is
compatible with a Klatskin tumor (hilar
cholangiocarcinoma)
Intrahepatic Biliary Dilatation: Axial CT
of the abdomen at a more superior level
reveals significant intrahepatic biliary
dilatation (yellow arrows)
56. Small hilar cholangiocarcinoma (Arrowhead) producing obstruction of the right
posteral sectoral duct (Short arrow). Right anterior sectoral duct (long arrow) and
left hepatic duct. (A) Thick oblique coronal MRCP. (B) Axial portal phase CT (C)
Longitudinal US. (D) Transverse color Doppler US (Open arrow, normal left portal
vein).
57. CT- abdomen- intra & extra-hepatic bile duct dilatation to the
level of the hepatic hilium. Suggestion of 2cm mass at hilium
cholangiocarcinoma-(Klatskin tumour)