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FISH, PDGFRB, 5q33.1

Test Summary

FISH testing with the PDGFRB probe allows detection of translocations involving PDGFRB and another chromosome region (usually a tyrosine kinase coding gene). Fusion of PDGFRB with a tyrosine kinase coding gene leads to kinase activation.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

3 mL bone marrow or 5 mL whole blood collected in a 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.
1-3 mL bone marrow in transport medium or 3-5 mL whole blood in a sodium heparin tube (green top, royal blue top, tan top). Formalin fixed paraffin embedded tumor biopsy or 5 mm x 5 mm fresh tumor biopsy in transport medium.

Note: 100-300 interphase cells are microscopically analyzed for probe signal patterns indicating rearrangement of 5q33.1.
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 collected in: Transport medium, sodium heparin (royal blue-top) tube, or sodium heparin lead free (tan-top) tube • Whole blood collected in: Sodium heparin (royal blue-top) tube or sodium heparin lead free (tan-top) tube • 5x5 mm fresh tumor tissue in transport medium • 5x5 mm tumor tissue in formalin-fixed paraffin-embedded tissue block

Unacceptable Specimens

N/A

Order Code

PDGFSH

EPIC (Premier) Code

LAB6341

Includes

N/A

CPT Code

  • 88271 (x2)
  • 88275

Billing Code

  • 670919
  • 670920

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

Interpretive report

Setup Schedule / Expected Turnaround Time

Daily; Report available: 5 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

3 mL bone marrow or 5 mL whole blood collected in a 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.
1-3 mL bone marrow in transport medium or 3-5 mL whole blood in a sodium heparin tube (green top, royal blue top, tan top). Formalin fixed paraffin embedded tumor biopsy or 5 mm x 5 mm fresh tumor biopsy in transport medium.

Note: 100-300 interphase cells are microscopically analyzed for probe signal patterns indicating rearrangement of 5q33.1.
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 collected in: Transport medium, sodium heparin (royal blue-top) tube, or sodium heparin lead free (tan-top) tube • Whole blood collected in: Sodium heparin (royal blue-top) tube or sodium heparin lead free (tan-top) tube • 5x5 mm fresh tumor tissue in transport medium • 5x5 mm tumor tissue in formalin-fixed paraffin-embedded tissue block

Unacceptable Specimens

N/A

Billing

CPT Code

  • 88271 (x2)
  • 88275

Billing Code

  • 670919
  • 670920

CPT Statement

Result Information

Methodology

Fluorescence In Situ Hybridization (FISH)

Testing Laboratory

N/A

Reference Range

Interpretive report

Setup Schedule / Expected Turnaround Time

Daily; Report available: 5 days