Also known as: Pediatric hepatoblastoma, childhood liver cancer.
What is hepatoblastoma?
A hepatoblastoma is a rare tumor (cancerous- spreads) that grows from the cells of the liver. It’s the most common of liver cancers in childhood, occurring during the first 18 months of life (infants to 5 years of age), in mostly white children, boys, and those born prematurely of low birth weight.
What causes hepatoblastoma?
While the cause is unknown, certain genetic (familial adenomatous polyposis, Beckwith-Wiedemann syndrome) and other medical conditions can put children at a greater risk of getting hepatoblastoma (e.g. hemihyperplasia, hepatitis B infection, biliary atresia).
What are the signs/symptoms of hepatoblastoma?
Signs and symptoms depend on the size of the tumor and whether or not it has spread. They include; a lump in the liver, a swollen abdomen, fever, weight loss, vomiting, reduced appetite, jaundice with yellow skin and eyes, itchiness and/or pale skin color (anemia), and back pain.
What are hepatoblastoma care options?
Treatments include surgery and one or more types of chemotherapy.
Reviewed by: Jack Wolfsdorf, MD, FAAP
This page was last updated on: 6/21/2019 2:20:24 AM
Nicklaus Children's Hospital and the Miami Cancer Institute, part of Baptist Health South Florida, are again collaborating for The Caring for Kids with Cancer Symposium. Learn more.