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

Nevil Kadakia; Steven J. Lobritto; Nadia Ovchinsky; Helen E. Remotti; Darrell J. Yamashiro; Darrell J. Yamashiro; Darrell J. Yamashiro; Jean C. Emond; Mercedes Martinez

doi:10.3389/fped.2017.00114

Frontiers in Pediatrics (Jun 2017)

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

Nevil Kadakia,
Steven J. Lobritto,
Nadia Ovchinsky,
Helen E. Remotti,
Darrell J. Yamashiro,
Darrell J. Yamashiro,
Darrell J. Yamashiro,
Jean C. Emond,
Mercedes Martinez

Affiliations

Nevil Kadakia: Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York, NY, United States
Steven J. Lobritto: Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York, NY, United States
Nadia Ovchinsky: Department of Pediatrics, Children’s Hospital of Montefiore, Bronx, NY, United States
Helen E. Remotti: Department of Pathology and Cell Biology, Columbia University College of Physicians and Surgeons, New York, NY, United States
Darrell J. Yamashiro: Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York, NY, United States
Darrell J. Yamashiro: Department of Pathology and Cell Biology, Columbia University College of Physicians and Surgeons, New York, NY, United States
Darrell J. Yamashiro: Department of Surgery, Columbia University College of Physicians and Surgeons, New York, NY, United States
Jean C. Emond: Department of Surgery, Columbia University College of Physicians and Surgeons, New York, NY, United States
Mercedes Martinez: Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York, NY, United States

DOI: https://doi.org/10.3389/fped.2017.00114
Journal volume & issue: Vol. 5

Abstract

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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.

Published in Frontiers in Pediatrics

ISSN: 2296-2360 (Online)
Publisher: Frontiers Media S.A.
Country of publisher: Switzerland
LCC subjects: Medicine: Pediatrics
Website: http://journal.frontiersin.org/journal/pediatrics

About the journal

Abstract

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