A Challenging Case of Hepatoblastoma Concomitant with Autosomal Recessive Polycystic Kidney Disease and Caroli Syndrome-Review of the Literature.
Publication/Presentation Date
1-1-2017
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.
Volume
5
First Page
114
Last Page
114
ISSN
2296-2360
Published In/Presented At
Kadakia, N., Lobritto, S. J., Ovchinsky, N., Remotti, H. E., Yamashiro, D. J., Emond, J. C., & Martinez, M. (2017). A Challenging Case of Hepatoblastoma Concomitant with Autosomal Recessive Polycystic Kidney Disease and Caroli Syndrome-Review of the Literature. Frontiers in pediatrics, 5, 114. https://doi.org/10.3389/fped.2017.00114
Disciplines
Medicine and Health Sciences
PubMedID
28638817
Department(s)
Department of Medicine
Document Type
Article
COinS