Abstract
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.
Original language | English (US) |
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Article number | 114 |
Journal | Frontiers in Pediatrics |
Volume | 5 |
DOIs | |
State | Published - Jun 7 2017 |
Keywords
- Autosomal recessive polycystic kidney disease
- Caroli syndrome
- Congenital hepatic fibrosis
- Hepatoblastoma
- Hepatorenal fibrocystic diseases
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health