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FISH, NHL, BCL6 3q27 Rearrangement

Test Summary

Chromosomal rearrangements of the BCL6 gene located at 3q27 are found in B-cell non-Hodgkin lymphomas including diffuse large cell lymphoma (DLCL),follicular lymphoma (FL) and marginal zone B-cell lymphoma (MZBCL). DLCL is an aggressive disease that usually responds well to multiagent chemotherapy. Up to 30% of DLCL demonstrate recurrent rearrangements involving the BCL6 gene.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

3 mL bone marrow or 5 mL whole blood collected in sodium heparin (green-top) tube

Minimum Volume

1 mL bone marrow • 3 mL whole blood

Instructions

Clinical history and reason for referral are required with test order. Prior therapy and transplant history should be provided with test order.
3 mL bone marrow in transport media or sodium heparin (green-top) tube or 5 mL whole blood collected in a sodium heparin (green-top) tube, or 5x5 mm fresh tumor biopsy in transport medium, or formalin-fixed, paraffin-embedded tissue. Ship at room temperature.

If results are not possible, the test order may be canceled and replaced with a Cytogenetics Communication.

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Room temperature

Specimen Stability

  • Specimen viability decreases during transit. Send specimen to testing lab for viability determination. Do not freeze. Do not reject.

Limitations

N/A

Other Acceptable Specimens

Bone marrow or whole blood collected in: sodium heparin (royal blue-top) or sodium heparin lead-free (tan-top) tube • 5x5mm fresh tumor tissue collected in culture transport media, or Formalin-fixed, paraffin-embedded tissue block

Unacceptable Specimens

N/A

Order Code

BCL63Q

EPIC (Premier) Code

LAB6136

Includes

N/A

CPT Code

  • 88275
  • 88271 (x2)

Billing Code

  • 670932
  • 670933

CPT Statement

Methodology

Fluorescence In Situ Hybridization (FISH)

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly VA, 20153

Department

Reference Testing

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Daily; Report available: 7 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

3 mL bone marrow or 5 mL whole blood collected in sodium heparin (green-top) tube

Minimum Volume

1 mL bone marrow • 3 mL whole blood

Instructions

Clinical history and reason for referral are required with test order. Prior therapy and transplant history should be provided with test order.
3 mL bone marrow in transport media or sodium heparin (green-top) tube or 5 mL whole blood collected in a sodium heparin (green-top) tube, or 5x5 mm fresh tumor biopsy in transport medium, or formalin-fixed, paraffin-embedded tissue. Ship at room temperature.

If results are not possible, the test order may be canceled and replaced with a Cytogenetics Communication.

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Room temperature

Specimen Stability

  • Specimen viability decreases during transit. Send specimen to testing lab for viability determination. Do not freeze. Do not reject.

Limitations

N/A

Other Acceptable Specimens

Bone marrow or whole blood collected in: sodium heparin (royal blue-top) or sodium heparin lead-free (tan-top) tube • 5x5mm fresh tumor tissue collected in culture transport media, or Formalin-fixed, paraffin-embedded tissue block

Unacceptable Specimens

N/A

Billing

CPT Code

  • 88275
  • 88271 (x2)

Billing Code

  • 670932
  • 670933

CPT Statement

Result Information

Methodology

Fluorescence In Situ Hybridization (FISH)

Testing Laboratory

N/A

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Daily; Report available: 7 days