Test Code LAB7872 (L/L phenotype) Flow Cytometry/ Leukemia/Lymphoma Assessment
Additional Codes
If quantitative testing is desired, a CD4, CD4/CD8, or a T&B Cell panel can be ordered. These will only be performed on whole blood samples collected in lavender and yellow top tubes (both are requested for testing). It is preferable to have samples < 24 hours old.
Performing Laboratory
NRL-Molecular Diagnostics
Methodology
Flow Cytometry
Includes flow cytometric analysis with a panel of lymphocyte- and/or myeloid-lineage associated antigens. The appropriate panel is chosen by a Christian Hospital pathologist based on clinical information, specimen type, specimen volume, cellular characteristics, and/or morphologic review. This test also includes review of morphology and morphologic correlation with immunophenotypic results.
Useful for immunophenotyping of blood, body fluids, bone marrow, or tissue of patients with suspected leukemia/lymphoma.
Specimen Requirements
Forms: Christian Hospital Hematopathology-Bone Marrow in Requisition in Special Instructions
Note: Name and telephone number of the ordering physician and a brief history are essential to achieve a consultation fully relevant to the ordering physician’s needs.
Specimen must arrive within 24 hours of collection.
Whole Blood
Lavender EDTA and Yellow ACD whole blood are required.
Dark Green Sodium Heparin are also acceptable.
Specimen Type: EDTA whole blood
Container/Tube: Lavender top (EDTA)
Specimen Volume: 5 mL
Collection Instructions:
1. Draw date is required.
Specimen Type: ACD Solution whole blood
Container/Tube: Yellow Top
Specimen Volume: 10 mL
Collection Instructions:
1. Draw date is required.
Specimen Type: Body fluid
Container/Tube: Plastic container
Specimen Volume: 1 mL
Collection Instructions: Label specimen as body fluid.
Additional Information: Indicate on requisition “for flow cytometric leukemia/lymphoma analysis.”
Bone Marrow
EDTA and sodium heparin bone marrow are required.
Specimen Type: EDTA bone marrow
Container/Tube: Lavender top (EDTA)
Specimen Volume: 2-3 mL
Collection Instructions:
1. Collection date is required.
2. Label specimen as EDTA bone marrow.
Specimen Type: Sodium heparin bone marrow
Container/Tube: Green top (sodium heparin)
Specimen Volume: 2-3 mL
Collection Instructions:
1. Collection date is required.
2. Label specimen as sodium heparin bone marrow.
Specimen Type: Tissue
Container/Tube: Sterile container
Specimen Volume: 1 cm3 or larger biopsy (or as much tissue as is feasible depending on procedure and/or tissue source).
Collection Instructions:
1. Place specimen intact (do not mince) in 15 mL of tissue culture medium (eg, RPMI, or equivalent). Specimen cannot be fixed.
2. Label specimen as tissue.
3. Tissue samples collected on Friday must be received in the laboratory by noon.
Reference Values
An interpretive report will be provided.
Day(s) Test Set Up
Monday through Friday
Turnaround Time:
48 hours
Specimen Transport Temperature
Ambient/Frozen NO-Blood, Body Fluid, Bone Marrow
Refrigerate-Tissue specimens
Specimen Requirements Additional Information
Instructions for the Laboratory:
If NetworkReferenceLab receives an inquiry, refer call to the Flow Cytometry Laboratory. Alert flow cytometry staff and/or pathologist of the request and ask them to consult with the caller.
Test Classification and CPT Coding
Test Classification:This test was developed and its performance characteristics determined by Christian Hospital Flow Cytometry & Pathology Departments. St. Louis, MO. It has not been cleared or approved by the U.S. Food and Drug Administration.
CPT Code:
88184-Flow cytometry, cell surface, cytoplasmic, first marker
88185-Each additional marker
88187-Pathologist interpretation
88188-Pathologist interpretation
88189-Pathologist interpretation
Triage Panel
88184-First marker
88185 x 8-Each additional marker
88188-Pathologist interpretation
Each specimen submitted for flow cytometry analysis is screened with the triage panel, whenever possible.
At the discretion of the pathologist, additional panels or markers may be analyzed when warranted. An interpretive report is provided with an explanation of testing.