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   <subfield code="a">Biphenotypic hepatic tumors: imaging findings and review of literature</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Michael Wells, Sudhakar Venkatesh, Vishal Chandan, Jeff Fidler, Joel Fletcher, Geoffrey Johnson, David Hough, Lewis Roberts]</subfield>
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   <subfield code="a">Purpose: To describe imaging findings in biphenotypic hepatic tumors (BPT) and a proposal for new imaging classification based on contrast-enhanced imaging. Methods: Retrospective review of CT, MRI, PET/CT, and ultrasound findings in 39 patients with histologically confirmed BPT was performed. Tumor markers including AFP, L3 fraction, CA 19.9, CA 125, and CEA were recorded. Based on the dynamic enhancement features, BPT were categorized into 4 enhancement patterns (Types 1-4). Enhancement patterns were correlated with other imaging findings and tumor markers. Imaging features and tumor markers that were not consistent with diagnosis of hepatocellular carcinoma or intrahepatic cholangiocarcinoma based on enhancement pattern were considered discordant findings. Results: Enhancement patterns in 29 patients (CT/MR) included 23 Type 2 (continuous peripheral rim of late arterial hyperenhancement with washout or fade in portal venous and/or delayed phases, ±delayed central enhancement) and 2 of each Types 1, 2, and 3. Discordant imaging findings were present in two patients with Type 2 pattern and in one patient with Type 1 pattern. Both AFP and CA 19.9 were elevated in 15 of 33 of patients. Tumor markers AFP and CA 19.9 were discordant in 17 of 21 patients with Type 2 pattern, two of two patients with Type 3 pattern. Most BPTs were markedly PET avid with average SUV max of 8.2. Most frequent ultrasound appearance is peripheral hypoechogenicity and central hyperechogenicity. Conclusions: BPT most commonly present with imaging features similar to cholangiocarcinoma or metastases. BPT can be suggested when imaging findings or tumor markers are discordant with the most likely diagnosis based on enhancement pattern.</subfield>
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   <subfield code="a">Springer Science+Business Media New York, 2015</subfield>
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   <subfield code="a">Biphenotypic hepatic tumor</subfield>
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   <subfield code="a">Computed tomography (CT)</subfield>
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   <subfield code="a">Magnetic resonance imaging (MRI)</subfield>
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   <subfield code="a">Positron emission tomography (PET)</subfield>
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   <subfield code="a">Wells</subfield>
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   <subfield code="u">Department of Radiology, College of Medicine, Mayo Clinic, 200 First St. SW, 55905, Rochester, MN, USA</subfield>
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   <subfield code="a">Venkatesh</subfield>
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   <subfield code="a">Chandan</subfield>
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   <subfield code="u">Department of Pathology, Mayo Clinic, Rochester, MN, USA</subfield>
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   <subfield code="a">Fidler</subfield>
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   <subfield code="t">Abdominal Imaging</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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