B-Cell Lymphoma, FISH, Tissue
Use
This test is useful for detecting recurrent common chromosome abnormalities associated with various B-cell lymphomas at diagnosis in paraffin-embedded tissue specimens. Genetic abnormalities have emerged as important prognostic markers and can aid in diagnosis. Fluorescence in situ hybridization (FISH) permits the detection of recurrent gene rearrangements associated with various chromosome translocations and inversions in B-cell lymphoma.
Special Instructions
Not provided.
Limitations
This test is not approved by the FDA and should be used as an adjunct to clinical and pathologic information. Fixatives other than formalin may not ensure successful FISH assays. Paraffin-embedded tissues that have been decalcified have approximate 50% success rate. Testing might be canceled if there is insufficient tumor tissue.
Methodology
Chromosomal / Cytogenetics (FISH)
Biomarkers
Chromosome t(2;8)(p12;q24.21)
ChromosomeUnknown CNV
Copy Number Region
LOINC Codes
- 101651-8 - BLYM Tiss FISH
- 50397-9 - Mol dx interp Bld/T Ql
- 69965-2 - Clinical cytogeneticist review
- 93356-4 - Cells w cytogenetic abnl Bld/T
- 62356-1 - Chrom analy result (ISCN)
- 42349-1
- 31208-2 - Specimen source
- 85298-8 - Struct incl in spec Spec
- 80398-1 - Unique ID Current sample
- 85069-3 - Lab test method
- 48767-8 - Annotation comment Imp
- 62364-5 - Test performance info Spec
- 18771-6 - Provider signing name
Result Turnaround Time
4-10 days
Related Documents
For more information, please review the documents below
Specimen
Tissue (FFPE)
Volume
Not provided
Minimum Volume
Not provided
Collection Instructions
Submit a formalin-fixed, paraffin-embedded tumor tissue block. Blocks with alternative fixation methods like Prefer or Bouin’s may be attempted but are less successful. Decalcified paraffin-embedded specimens have an approximate 50% success rate.
Causes for Rejection
Fresh tissue specimens will be rejected.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | Ambient preferred |
