Intrahepatic cholangiocarcinoma

ICD-10 Code C22.1

Intrahepatic cholangiocarcinoma

Definition

A carcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree. Grossly, the malignant lesions are solid, nodular, and grayish. Morphologically, the vast majority of cases are adenocarcinomas. Signs and symptoms include malaise, weight loss, right upper quadrant abdominal pain, and night sweats. Early detection is difficult and the prognosis is generally poor.

Also known as cholangiocarcinoma, intrahepatic, malignant, ICC, intrahepatic bile duct cancer (cholangiocarcinoma), intrahepatic bile duct carcinoma, intrahepatic carcinoma of bile duct, intrahepatic carcinoma of the bile duct, intrahepatic cholangiocarcinoma, intrahepatic cholangiocarcinoma (bile duct cancer), intrahepatic Cholangiocellular carcinoma — per MONDO

Also identified as

Affected Organs

Organ Involvement Source
Alimentary part of gastrointestinal system Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Alimentary part of gastrointestinal system Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Bile ducts Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Bile ducts Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Biliary system Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Biliary system Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Intrahepatic bile duct Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Liver Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Liver Disease Has Primary Anatomic Site NCIT · CC BY 4.0