FISH for B Lymphoblastic Leukemia Panel Bone Marrow




Test Mnemonic

FSBLLM

CPT Codes

  • 88271 - QTY (12)
  • 88275 - QTY (6)
  • 88291 - QTY (1)
  • 88237 - QTY (1)

Includes

  • FISH for BCRABL
  • FISH for MLL
  • FISH for t(12;21)(p13q22)
  • FISH for Trisomy 4 and 10
  • FISH for CRLF2M
  • FISH for CRIGHM

Performing Laboratory

Cleveland Clinic Laboratories

FDA Category

Analyte Specific Reagent


Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
2 - 3 mLBone marrowEDTA (Lavender)AmbientAmbient 

Alternate Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
2 - 3 mLBone marrowSodium heparin (Green)AmbientAmbient 

Stability

Environmental Condition Description
Ambient48 hours
RefrigeratedAcceptable
FrozenNot acceptable

Days Performed

4 days per week

Turnaround Time

5 - 7 days

Methodology

Name Description
Fluorescent In-Situ Hybridization (FISH) 

Clinical Info

The t(X;14)(p22.33;q32.33) or t(Y;14)(p11.32;q32.33) translocations, involving the CRLF2 and IGH genes, are cytogenetically-cryptic rearrangements. The CRLF2 gene is located within the pseudoautosomal region of the X and Y chromosomes. These rearrangements are associated with B-progenitor acute lymphoblastic leukemia (ALL) and Down syndrome ALL. They are present in approximately 19.8% of patients with extra copies of the X chromosome produced by high hyperdiploidy. CRLF2::IGH positive cells also have a high frequency (94%) of additional deletions which may reflect chromosomal instability. Although CRLF2::IGH is part of the BCR::ABL1-like ALL subtype, this rearrangement is not associated with it in all cases. In general, the prevalence of the CRLF2::IGH translocation increases with age.