Eosinophilia Panel by FISH (Temporary Delay as of 09/17/2021 - no referral available)
Aid in diagnosis and classification of hematopoietic neoplasms presenting with prominent eosinophilia. Does not detect rearrangements associated with chronic myelogenous leukemia.
Fluorescence in situ Hybridization (FISH)
New York DOH Approval Status
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)
Paraffin-embedded specimens. Clotted specimens.
Ambient: 48 hours; Refrigerated: 48 hours; Frozen: Unacceptable
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)
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.
88271 x3; 88275 x3
|Component Test Code*||Component Chart Name||LOINC|
|2002379||Eosinophilia Panel by FISH|
|2002380||EER FISH EOS P|
- FISH, Myeloproliferative Neoplasms (Eosinophilia)