Leukemia/Lymphoma Panel by Flow : 1003140

Message
Please submit a copy of the most recent CBC with differential report and any clinical information related to the patient's disease state. If available, send the lavender top tube used for the CBC w/diff. The CBC w/diff is needed for the reporting of the flow cytometry interpretative results.


Test Code
MDFCPLEUKPG or 1003140


Alias/See Also
Flow; Leukemia Panel; Immunophenotype; Immunophenotyping; Leukemia


CPT Codes
88184, 88185x 14 up to 23 or varies dependent on specimen type, 88189, additional testing may be added at the discretion of the Pathologist

Instructions
Peripheral blood in a green top sodium heparin tube (4-10 mL) or Bone Marrow aspirate in a green top sodium heparin tube (2-3 mL). A lavender top (EDTA) tube is acceptable if a green top tube is not available. Other acceptable specimens: Tissue, Fluid, or CSF (cerebrospinal fluid)


Transport Container
Blood or Bone Marrow: specimen must be received within 24 hours of collection. Do not centrifuge. Tissue samples should be placed in appropriate Tissue Transport Media (available on request). Submit fluid samples (desired: > or = 50 mL when possible) or CSF (desired: 2-3 mL) in a screw capped container or tube. Note: Smaller volumes of fluid samples may be accepted depending on source and cellularity of the specimen. Please contact the laboratory if the appropriateness of source or volume of sample is in question.


Transport Temperature
Blood or Bone Marrow: Ambient temperature within 24 hours. Specimen can be refrigerated if not transported immediately. Do not freeze. Protect from heat with a refrigerated cold (not frozen) pack. Tissue, Fluid or CSF: Ambient.


Specimen Stability
Lavender (EDTA): Ambient: 24 hours; Refrigerated: 48 hours; Frozen: Unacceptable

Green (Na Heparin): Ambient: 48 hours; Refrigerated: 48 hours; Frozen: Unacceptable

CSF: Ambient: 24 hours; Refrigerated: 48 hours; Frozen: Unacceptable

Body Fluid: Ambient: 24 hours; Refrigerated: 48 hours; Frozen: Unacceptable

Tissue in transport media: Ambient: 24 hours; Refrigerated: 48 hours; Frozen: Unacceptable


Methodology
Immunophenotyping by Flow Cytometry

Setup Schedule
Sunday - Saturday


Report Available
1-2 days


Limitations
Laboratory test results should always be considered in the context of clinical observations. This test was developed and its performance characteristics determined by med fusion. It has not been cleared or approved by the U.S. Food and Drug Administration
(FDA). The FDA has determined that such clearance or approval is not necessary. This test is used for clinical purposes. It should not be regarded as investigational for research. This laboratory is certified under the Clinical Laboratory Improvement Amendments
of 1988 (CLIA) as qualified to perform high complexity clinical laboratory testing.


Reference Range
An interpretive report will be provided.


Clinical Significance
Diagnosis and classification of neoplasms of hematopoietic and lymphoid origin.


Performing Laboratory
med fusion



The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.