A Challenging Case of Hepatoblastoma Concomitant with Autosomal Recessive Polycystic Kidney Disease and Caroli Syndrome—Review of the Literature

Frontiers in Pediatrics

Nevil Kadakia¹ 

关键词: hepatorenal fibrocystic diseases;    hepatoblastoma;    autosomal recessive polycystic kidney disease;    congenital hepatic fibrosis;    Caroli syndrome;   

DOI  :  10.3389/fped.2017.00114

学科分类：儿科学

来源: Frontiers

【 摘 要 】

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.

【 授权许可】

CC BY