CHOLANGIOCARCINOMA
CHOLANGIOCARCINOMA
CHOLANGIOCARCINOMA
SGD B08
INTRODUCTION
CHOLANGIOCARCINOMA
Malignancy of the epithelium of the biliary tree.
The most common biliary tract malignancy.
Affect one in every 100,000 people per year in
the United States.
Slightly more prevalent in males than females
(1.3:1.0) and usually affects patients in the fifth
to seventh decade of life.
Represents a diverse group of epithelial cancers
united by late diagnosis and poor outcomes
prognosis is considered dismal.
Treatment and long-term prognosis are
dependent upon the location of the mass.
Surgical treatment is the preferred option.
DEFINITION
CHOLANGIOCARCINOMA
Intrahepatic
Cholangiocarcinoma(iCCA)
Perihilar
Cholangiocarcinoma(pCCA)
Distal Cholangiocarcinoma(dCCA)
ETIOLOGY
Cholangiocarcinoma has developed without an
identifiable etiology
Risk factors are
primary sclerosing cholangitis (PSC)
Viral hepatitis (HCV & HBV)
Parasitic infections (Opisthorchis viverrini and
Clonorchis sinensis )
Cholelithiasis and choledocholithiasis
Toxins (smoking, alcohol)
Diabetes
PATHOPHYSIOLOGY
Cholangiocarcinoma
assosiated with:
GENETIC OR
INFLAMMATION MOLECULAR
THEORY THEORY
INFLAMMATION THEORY
Chronic
Inflammator Nitrosative DNA Carcinogene
Inflammatio iNOS active
y Cytokines stress damage sis
n
INFLAMMATION THEORY
Increase
Activate
IL-6 expression
STAT3
of MCL1
CCA
developme
nt increase
Increase
Cell
Proliferation
CHOLESTASIS
Tumor
ERBB2
Formation
Bile Activate
Acid EGFR Invasivenes
HGF s and Tumor
Metastasis
GENETIC OR MOLECULAR THEORY
CODON 12
K-ras CODON 13
MUTATION
CODON 61
OF p53
TGF
SMAD4 signalling
network
SIGN & SYMPTOMS
Mostly asymptomatic.
Unspecific symptoms:
Malaise
Abdominal pain
Weight loss
Hepatomegaly
Tumor mass
Dilated gallbladder
Symptoms that can present on extrahepatic patient are:
Dark urine
Pruritis
Painless jaundice
Pale stools
DIAGNOSIS
DIAGNOSIS
Klatskin
iCCA pCCA dCCA
Tumors
Bismuth-
Tumor Tumor
Corlette
marker marker
system
Genetic Genetic
marker marker
DIFFERENTIAL DIAGNOSIS
GALLBLADDER CANCER
HEPATOCELLULAR CARCINOMA
CHOLANGITIS AND
CHOLEODOCHOLITHIASIS
MANAGEMENT
Treatment Cholangiocarcinoma
Surgical
Transplantation
Resection
Photodynamic
Therapy (PDT)
Radiation
Chemotherapy
Therapy
Prevention Cholangiocarcinoma
enhancing
knowledge
about disease
and risk factor
PROGNOSIS
Prognosis
remains poor
Intrahepatic cholangiocarcinoma Extrahepatic cholangiocarcinoma
Stage 5-year relative Stage 5-year relative
survival survival
Localiz 15% Localiz 30%
ed ed
Region
Source: 6% Society
American Cancer Region 24%
al al
Factors that affecting patient survival have been impeded by:
Distant 2% Distant 2%
lack of disease-specific symptoms in early stages
surgical resection not being an appropriate treatment option
high rates of tumor recurrence following surgical resection