#ExistRefRangeSet>
Reference Interval:
#ExistRefRange>By report
*ExistRefRange>
#ExistRefRangeTable> | Test Number
| Components
| Reference Interval
| | | Alpha Fetoprotein Total
| 0-15 ng/mL
| | | Alpha Fetoprotein L3 Percent
| 0-9.9 percent
|
*ExistRefRangeTable>
|
*ExistRefRangeSet>
#ExistInterpDataSet>
| Interpretive Data: |
#ExistInterpData>The µTASWako method is used. Results obtained with different assay methods or kits cannot be used interchangeably. The AFP L3 Percent assay is intended as a risk assessment for the development of hepatocellular carcinoma in patients with chronic liver diseases. Patients with elevated serum AFP-L3 percent should be more intensely evaluated for evidence of hepatocellular carcinoma since elevated values have been shown to be associated with a seven-fold increase in the risk for developing hepatocellular carcinoma within 21 months. For pregnant females, the result is not interpretable as a tumor marker.
*ExistInterpData>
|
*ExistInterpDataSet>
#ExistCPT>
| CPT Code(s): |
82107
|
*ExistCPT>
#ExistCrossReferences>
Cross References: |
AFP (Liver Cancer) (Alpha Fetoprotein, Total and L3 Percent), AFP-L3% (Alpha Fetoprotein, Total and L3 Percent), Alpha Fetoprotein (Liver Cancer) (Alpha Fetoprotein, Total and L3 Percent), Alpha Fetoprotein, Total and L3 Percent (Alpha Fetoprotein, Total and L3 Percent), Alpha-Fetoprotein (AFP) L3% and Total, Hepatocellular Carcinoma Tumor Marker, Serum (Alpha Fetoprotein, Total and L3 Percent)
, Hepatocellular Carcinoma AFP (Alpha Fetoprotein, Total and L3 Percent) |
*ExistCrossReferences>