Perihilar cholangiocarcinoma

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Perihilar cholangiocarcinoma

ORPHA:99978Disease

Also called Hilar CCA · Hilar cholangiocarcinoma · Klatskin tumor

What it is

Klatskin tumor is an extra-hepatic cholangiocarcinoma (CCA) arising in the junction of the main right or left hepatic ducts to form the common hepatic duct.

Key facts

Prevalence
1-9 / 100 000 (Europe)
Age of onset
Adult
Inheritance
Not applicable
Classified as
Disease

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

ICD-10 codes

C24.0filed under a broader ICD-10 category — shared with 3 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

GARD 10175MESH D018285MONDO 0003345UMLS C0206702

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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