ARUP's Laboratory Test Directory

bcl-2/JH, t(14;18) Translocation by PCR, Tissue : 0055619

Mnemonic: BCL2C-T

Methodology: Polymerase Chain Reaction
Performed: DNA isolation: Sun-Sat; Assay: Varies
Reported: 2-7 days
Specimen Required: Collect:  Fresh tissue. Freeze immediately.

Transport:  100 mg or 0.5-2.0 cm3 tissue, frozen on dry ice.

Remarks:  Formalin-fixed, paraffin-embedded tissue can be submitted, but it is not an optimal specimen source.

Stability:  Ambient: Unacceptable; Refrigerated: 2 hours; Frozen: 1 year
Reference Interval:
 
Test Number Components Reference Interval
 bcl-2/JH, t(14;18) Translocation Major Breakpoint Region (MBR), Tissue Negative: bcl-2/JH major breakpoint region gene rearrangement is not detected.
Positive: bcl-2/JH major breakpoint region gene rearrangement is detected.
 bcl-2/JH, t(14;18) Translocation Minor Cluster Region (MCR), Tissue Negative: bcl-2/JH minor cluster region gene rearrangement is not detected.
Positive: bcl-2/JH minor cluster region gene rearrangement is detected.

Interpretive Data: By report

Please refer to Statement B in the Compliance Statements section in the front of the Laboratory Test Directory.
Note: A positive result indicates the presence of a bcl-2/JH t(14;18) chromosomal translocation.  A negative result does not entirely exclude the presence of a bcl-2/JH chromosomal t(14;18) translocation.

Comment: The chromosomal translocation t(14;18) or bcl-2 gene rearrangement is present in approximately 90% of follicular lymphomas and in a significant minority (10-30%) of diffuse large-cell lymphomas of B-cell lineage. Since most bcl-2 breakpoints cluster at the major breakpoint region (~60%) or minor cluster region (~10%), this PCR assay is capable of detecting a majority of bcl-2/JH gene rearrangements. However, some breakpoints occur at distant loci and will not be identified by this particular test.
CPT Code(s): 83891 Isolation; 83898 x6 Amplification; 83894 x3 Gel separation; 83912 Interpretation and report - Additional CPT code modifiers may be required for procedures performed to test for oncologic or inherited disorders.
 
 

 

 

 
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