Myelodysplastic Syndrome, Fluorescence <i>in situ</i> Hybridization (FISH)
Myelodysplastic Syndrome, Fluorescence in situ Hybridization (FISH)
    
Number
510599
CPT
88271 (x4); 88275; 88291
Related Information
  • Leukemia / Lymphoma Management Test Reference Chart
  • Synonyms
    MDS ; Myelodysplastic Syndrome FISH
    Special Instructions
    Indicate pertinent clinical diagnosis and previous cytogenetic studies on the request form. This test is for use on blood samples when no results are available from chromosome analysis and should not be ordered in conjunction with the preferred chromosome analysis.
    Specimen
    Blood, bone marrow, fixed-cell pellet from a cytogenetic analysis, or slides prepared from a cytogenetic analysis
    Volume
    Pediatrics: 3-5 mL blood, adults: 10 mL blood; 1-3 mL bone marrow, four slides, one fixed-cell pellet
    Minimum Volume
    1 mL blood (adult/pediatric), 1 mL bone marrow, or two slides
    ContainerContainer - Updated May 9 2008
    Green-top (heparin) tube; pediatric Vacutainer® is optimal or lavender-top (EDTA) tube
    Storage Instructions
    Maintain specimen at room temperature.
    Causes for Rejection
    Broken Vacutainer®; broken slides
    Use
    Diagnostic test for myelodysplastic syndrome. Principle use is for interphase analysis of cases with no or low mitotic activity in cytogenetic analysis or interphase analysis from blood in cases of inaspirable bone marrow. Detection rate is ~80% of clones detected in cytogenetic analysis.
    Methodology
    Fluorescence in situ hybridization (FISH) for 5q, 7q, 8, and 20q

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