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

Frontiers in Pediatrics

Helen E. Remotti¹  Nadia Ovchinsky²  Mercedes Martinez³  Nevil Kadakia³  Steven J. Lobritto³  Darrell J. Yamashiro⁴  Jean C. Emond⁴ 

[1] Department of Pathology and Cell Biology, Columbia University College of Physicians and Surgeons, New York, NY, United States;Department of Pediatrics, Children’s Hospital of Montefiore, Bronx, NY, United States;Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York, NY, United States;Department of Surgery, Columbia University College of Physicians and Surgeons, New York, NY, United States;

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

DOI  :  10.3389/fped.2017.00114

来源: DOAJ

【 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】

Unknown