Abstract
Fibrolamellar carcinoma (FLC) is a rare variant of hepatocellular carcinoma, occurring in children and young adults without underlying liver disease. The diagnosis is based on morphological characteristics of the tumor, supplemented by immunohistochemistry and/or genetic testing. Recently, the presence of a characteristic DNAJB1-PRKACA fusion gene has been associated with FLC. Herein, we report a case of FLC presenting as peritoneal carcinomatosis in a 14-year-old female. Interestingly, no liver tumor was seen on imaging, and an alternative possibility is that the tumor arose outside the liver as a hepatoid carcinoma with fibrolamellar features.
Keywords:
cancer genetics; liver; pediatric hematology/oncology; tumors.
© 2019 Wiley Periodicals, Inc.
MeSH terms
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Adolescent
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use
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Carcinoma, Hepatocellular / drug therapy
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Carcinoma, Hepatocellular / genetics
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Carcinoma, Hepatocellular / secondary*
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Cyclic AMP-Dependent Protein Kinase Catalytic Subunits / genetics*
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Female
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Gene Rearrangement
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HSP40 Heat-Shock Proteins / genetics*
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Humans
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Neoplasms, Unknown Primary / drug therapy
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Neoplasms, Unknown Primary / genetics
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Neoplasms, Unknown Primary / pathology*
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Peritoneal Neoplasms / drug therapy
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Peritoneal Neoplasms / genetics
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Peritoneal Neoplasms / secondary*
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Prognosis
Substances
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DNAJB1 protein, human
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HSP40 Heat-Shock Proteins
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Cyclic AMP-Dependent Protein Kinase Catalytic Subunits
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PRKACA protein, human
Supplementary concepts
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Fibrolamellar hepatocellular carcinoma