| Literature DB >> 29420370 |
Julie Bennett1, Melanie Kirby-Allen1, Vicky Ng2, John S Waye3, Catherine T Chung4, Furqan Shaikh1.
Abstract
Hepatoblastoma is the most common hepatic malignancy of childhood with known genetic predispositions and perinatal risk factors, with rare case reports occurring in the setting of cirrhosis. This case describes a young patient with cirrhosis attributed to early-onset hereditary hemochromatosis who was diagnosed with hepatoblastoma with uncommon histologic findings, evidence of chemotherapy resistance who ultimately succumbed to her disease. It is important to consider diagnoses beyond hepatocellular carcinoma in this scenario and consider early biopsy. With atypical histology, the tumor may respond poorly to conventional treatment and aggressive surgery or intensive therapy should be contemplated.Entities:
Mesh:
Year: 2019 PMID: 29420370 DOI: 10.1097/MPH.0000000000001097
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289