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Eosinophilia Panel by FISH
Ordering Recommendation
Aid in diagnosis and classification of hematopoietic neoplasms presenting with prominent eosinophilia. Does not detect rearrangements associated with chronic myelogenous leukemia.
New York DOH Approval Status
Specimen Required
Non-diluted bone marrow aspirate collected in a heparinized syringe. Also acceptable: Green (Sodium Heparin).
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)
Room temperature.
Paraffin-embedded specimens. Clotted specimens.
Ambient: 48 hours; Refrigerated: 48 hours; Frozen: Unacceptable
Methodology
Fluorescence in situ Hybridization (FISH)
Performed
Sun-Sat
Reported
3-10 days
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.
Analyte Specific Reagent (ASR)
Note
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.
Hotline History
CPT Codes
88271 x3; 88275 x3
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 2002379 | Eosinophilia Panel by FISH | |
| 2002380 | EER FISH EOS P |
Aliases
- FISH, Myeloproliferative Neoplasms (Eosinophilia)
