Test Code LAB0209863 Immunoglobulin Gene Rearrangement, PCR, Bone Marrow
Additional Codes
Mayo Test ID |
---|
BCGBM |
Performing Laboratory
Mayo Clinic Laboratories in RochesterUseful For
Determining whether a B-cell or plasma cell population is polyclonal or monoclonal using bone marrow specimens
Identifying neoplastic cells as having B-cell or plasma cell differentiation
Monitoring for a persistent neoplasm by detecting an immunoglobulin gene rearrangement profile similar to a previous neoplastic specimen
Special Instructions
Method Name
Polymerase Chain Reaction (PCR)
Reporting Name
Immunoglobulin Gene Rearrange, BMSpecimen Type
Bone MarrowShipping Instructions
Specimen must arrive within 7 days of collection.
Specimen Required
Container/Tube:
Preferred: Lavender top (EDTA)
Acceptable: Yellow top (ACD)
Specimen Volume: 2 mL
Collection Instructions:
1. Invert several times to mix bone marrow.
2. Send bone marrow specimen in original tube. Do not aliquot.
Specimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Bone Marrow | Ambient (preferred) | 7 days | |
Refrigerated | 7 days |
Reject Due To
Gross hemolysis | Reject |
Moderately to severely clotted | Reject |
Reference Values
An interpretive report will be provided.
Interpretation
An interpretive report will be provided.
Results will be characterized as positive, negative, or indeterminate for a clonal B-cell population.
The interpretation of the presence or absence of a predominant immunoglobulin gene rearrangement profile is sometimes subjective. These results must always be interpreted in the context of other clinicopathologic information to determine the significance of the result.
The detection of a clonal immunoglobulin gene rearrangement by this test is not synonymous with the presence of a B-cell or plasma cell neoplasm.
Day(s) Performed
Monday through Friday
Report Available
5 to 10 daysSpecimen Retention Time
Bone marrow: 2 weeks; Extracted DNA: 3 monthsTest Classification
This test was developed using an analyte specific reagent. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
81261-IGH (Immunoglobulin heavy chain locus) (eg, leukemias and lymphomas B-cell), gene rearrangement analysis to detect abnormal clonal populations; amplified methodology (eg. polymerase chain reaction)
81264-IGK (Immunoglobulin kappa light chain locus) (eg, leukemia and lymphoma, B-cell) gene rearrangement analysis, evaluation to detect abnormal clonal populations
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
BCGBM | Immunoglobulin Gene Rearrange, BM | 61113-7 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
19894 | Final Diagnosis: | 22637-3 |
608949 | Signing Pathologist | 19139-5 |
Forms
1. Hematopathology Patient Information (T676)
2. If not ordering electronically, complete, print, and send a Hematopathology/Cytogenetics Test Request (T726) with the specimen.