EPIC Lab Number

LAB58366

Collect

Non-diluted bone marrow aspirate collected in a heparinized syringe. Also acceptable: Green (Sodium Heparin).

Additional Requirements

Collect:   (Sodium Heparin) Green
Auto Lab Accepts:
Tube Types | East Side Clinical Laboratory

Unacceptable Conditions

Paraffin-embedded specimens. Clotted specimens.

Specimen Preparation

Bone Marrow: Transfer 3 mL bone marrow to a Green (Sodium Heparin) (Min: 1 mL).
Whole Blood: Transport 5 mL whole blood. (Min: 2 mL)

Ordering Recommendations

Aid in diagnosis and classification of hematopoietic neoplasms presenting with prominent eosinophilia. Does not detect rearrangements associated with chronic myelogenous leukemia.

Storage/Transport Temperature

Room temperature.

Stability (from collection to initiation)

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

Performed

Sun-Sat

Reported

3-10 days

Notes

A processing fee will be charged if this procedure is canceled, at the client's request, after the test has been set up, or if the specimen integrity is inadequate to allow culture growth. The fee will vary based on specimen type.

Other specimen types may be acceptable, contact the Cytogenetics Laboratory for specific specimen collection and transportation instructions.

If cell pellets or dropped cytogenetic slides are submitted, processing fee will not apply.

This test must be ordered using Oncology test request form #43099 or through your ARUP interface.

Methodology

Fluorescence in situ Hybridization (FISH)

Synonyms

  • FISH, Myeloproliferative Neoplasms (Eosinophilia)

Additional Technical Information

  • Time Sensitive
  • Oncology Test Request Form Recommended (ARUP form #43099)

Reference Interval

By report

Interpretive Data

Probes included: PDGFR-alpha, PDGFR-beta, and FGFR1.

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

ARUP Test Code

2002378

CPT Codes

88271 x3; 88275 x3
Test Information

EPIC Lab Number

LAB58366

Collect

Non-diluted bone marrow aspirate collected in a heparinized syringe. Also acceptable: Green (Sodium Heparin).

Additional Requirements

Collect:   (Sodium Heparin) Green
Auto Lab Accepts:
Tube Types | East Side Clinical Laboratory

Unacceptable Conditions

Paraffin-embedded specimens. Clotted specimens.

Specimen Preparation

Bone Marrow: Transfer 3 mL bone marrow to a Green (Sodium Heparin) (Min: 1 mL).
Whole Blood: Transport 5 mL whole blood. (Min: 2 mL)

Ordering Recommendations

Aid in diagnosis and classification of hematopoietic neoplasms presenting with prominent eosinophilia. Does not detect rearrangements associated with chronic myelogenous leukemia.

Storage/Transport Temperature

Room temperature.

Stability (from collection to initiation)

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

Performed

Sun-Sat

Reported

3-10 days

Notes

A processing fee will be charged if this procedure is canceled, at the client's request, after the test has been set up, or if the specimen integrity is inadequate to allow culture growth. The fee will vary based on specimen type.

Other specimen types may be acceptable, contact the Cytogenetics Laboratory for specific specimen collection and transportation instructions.

If cell pellets or dropped cytogenetic slides are submitted, processing fee will not apply.

This test must be ordered using Oncology test request form #43099 or through your ARUP interface.

Methodology

Fluorescence in situ Hybridization (FISH)

Synonyms

  • FISH, Myeloproliferative Neoplasms (Eosinophilia)

Additional Technical Information

  • Time Sensitive
  • Oncology Test Request Form Recommended (ARUP form #43099)

Reference Interval

By report

Interpretive Data

Probes included: PDGFR-alpha, PDGFR-beta, and FGFR1.

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

ARUP Test Code

2002378

CPT Codes

88271 x3; 88275 x3