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

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...

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Bibliographic Details
Main Authors:	Nevil Kadakia, Steven J. Lobritto, Nadia Ovchinsky, Helen E. Remotti, Darrell J. Yamashiro, Jean C. Emond, Mercedes Martinez
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2017-06-01
Series:	Frontiers in Pediatrics
Subjects:	hepatorenal fibrocystic diseases hepatoblastoma autosomal recessive polycystic kidney disease congenital hepatic fibrosis Caroli syndrome
Online Access:	http://journal.frontiersin.org/article/10.3389/fped.2017.00114/full

Internet

http://journal.frontiersin.org/article/10.3389/fped.2017.00114/full

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

Internet

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