With more than 30 identified subtypes of T-cell neoplasms, diagnosis can be difficult. We offer a full portfolio of testing for T-cell lymphoma, including molecular panels, comprehensive fluorescence in situ hybridization (FISH) panels, and extensive immunohistochemistry (IHC) offerings to diagnose and monitor T-cell lymphoma.
In addition, our hematopathology team has extensive experience with T-cell neoplasms, providing guidance and answers for clients and patients worldwide.
T-cell lymphoma Test menu
Key testing
Highlights
Andrew Feldman, M.D., discusses the different tools and techniques Mayo Clinic Laboratories uses to accurately diagnose and classify T-cell lymphomas to help provide clinicians with the diagnostic answers they need to treat their patients.
When deemed clinically necessary, next-generation sequencing (NGS) can supplement standard-of-care morphology, phenotyping, and FISH testing to refine diagnosis. Our unique MayoComplete T-cell lymphoma panel evaluates 26 genes with known diagnostic, prognostic, or therapeutic value in various T-cell lymphoma subtypes.
While the molecular subclassification of T-cell lymphoma continues to evolve, there are specific patterns of mutation that can be observed in select subtypes, such as angioimmunoblastic T-cell lymphoma (AITL) and large granular lymphocytic leukemia (T-LGL). Recognition of these mutational profiles using the genes provided in our panel can inform on the differential diagnosis of rare or not otherwise specified T-cell lymphomas and guide the selection of a targeted treatment.
Key testing