| Literature DB >> 29286561 |
William J Hammond1,2, Gadi Lalazar2, James A Saltsman1,2, Benjamin A Farber1,2, Enrico Danzer1, Tshering C Sherpa2, Charles D Banda2, Jeffrey R Andolina3, Sasan Karimi4, Cameron W Brennan5,6, Michael S Torbenson7, Michael P La Quaglia1, Sanford M Simon2.
Abstract
Fibrolamellar hepatocellular carcinoma (FLHCC) is a rare liver malignancy in adolescents and young adults. Surgery is the mainstay of therapy for primary and metastatic disease. Most patients relapse, with development of both local and distant metastases. Brain metastases from solid tumors are rare in the pediatric and young adult population. Here, we document three patients with brain metastases from FLHCC, confirmed by histology and molecular characterization of the chimeric fusion DNAJB1-PRKACA, each necessitating neurosurgical intervention. These observations highlight the ability of FLHCC to metastasize to the brain and suggest the need for surveillance neuroimaging for patients with advanced-stage disease.Entities:
Keywords: adolescent and young adult tumors; brain; fibrolamellar; liver; rare tumors; tumor biology; tumors
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Year: 2017 PMID: 29286561 PMCID: PMC6028006 DOI: 10.1002/pbc.26919
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167