7-10 days
Test Updated:
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Test Overview
Interphase Fluorescence In Situ Hybridization (FISH)
This panel differentiates double-hit or triple-hit lymphomas (which have MYC rearrangements together with BCL2 and/or BCL6 rearrangements) from Burkitt lymphoma or diffuse large B-cell lymphoma. Double-hit and triple-hit lymphomas are difficult to classify morphologically without the aid of cytogenetics/FISH or IHC, and are associated with an aggressive course. Testing is indicated when B-cell lymphoma patients experience transformation, relapse, or refractory disease. MYC rearranges with an immunoglobulin partner in approximately 60% of MYC-rearranged DLBCL/HGBCL of which 75% are MYC/IGH fusion. In addition, a small subset of lymphomas with MYC rearrangement (4%) may be missed when using the MYC breakapart probe alone, but some of these cases may be detected using the MYC/IGH fusion probe set (PMID: 30523057). The FISH panel for high grade B-cell lymphoma includes MYC (8q24), IGH/MYC/CEN8 [t(8;14)], BCL2 (18q21) and BCL6 (3q27) translocations.
Interpretive report provided.
*Reference ranges may change over time. Please refer to the original patient report when evaluating results.
* Reference ranges may change over time. Please refer to the original patient report when evaluating results.
Specimen Requirements
Collect specimen in a sterile syringe rinsed with sodium heparin or a green top vacutainer (sodium heparin) tube. Invert several times to prevent clotting. Send at room temperature as soon as possible. Do not allow specimen to overheat or freeze. Please complete a MiChart test request and submit it with the specimen. A Cytogenetics Laboratory Requisition is available online at:http://www.pathology.med.umich.edu/handbook/Tables/UM_REQ_CYTOGENETICS….
Collect blood or bone marrow using aseptic technique. Place 2-5 mL blood or 1 - 3 mL bone marrow aspirate in a green top (sodium heparin) tube. Invert the tube several times to prevent clotting. Send at room temperature as soon as possible. Do not allow specimen to overheat or freeze. Clotted samples, samples containing <5 million dividing cells, and samples that are greater than 24 hours old are suboptimal.