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Fibrolamellar hepatocellular carcinoma

Disease definition

A rare variant of hepatocellular carcinoma (HCC) presenting in adolescents or young adults with no underlying liver disease. Clinical presentation is non specific, with abdominal mass, abdominal discomfort or pain, fatigue and weight loss. Patients can also be asymptomatic. HCC markers (alpha fetoprotein) are normal. Fibrolamellar HCC presents as a unique, well-delimited mass at imagery and a biopsy confirms the diagnosis, showing well-differentiated tumor cells surrounded by thick collagen bands.

ORPHA:401920

Classification level: Disorder
  • Synonym(s):
    • FHCC
    • Fibrolamellar hepatocarcinoma
  • Prevalence: -
  • Inheritance: Not applicable 
  • Age of onset: Adolescent, Adult
  • ICD-10: C22.0
  • ICD-11: 2C12.02  XH9Q35
  • OMIM: -
  • UMLS: C0334287
  • MeSH: C537258
  • GARD: -
  • MedDRA: -

  A summary on this disease is available in Deutsch (2020) Español (2020) Français (2020) Italiano (2020) Nederlands (2020)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.