We report a rare case of an 18-month-old female with autosomal recessive polycystic kidney disease, Caroli syndrome, and pure fetal type hepatoblastoma. The liver tumor was surgically resected with no chemotherapy given. Now 9 years post resection she demonstrates no local or distant recurrence and stable renal function.
- Autosomal recessive polycystic kidney disease
- Caroli syndrome
- Congenital hepatic fibrosis
- Hepatorenal fibrocystic diseases
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health