4.7 Article

Improved reliability of lymphoma diagnostics via PCR-based clonality testing:: -: Report of the BIOMED-2 concerted action BHM4-CT98-3936

Journal

LEUKEMIA
Volume 21, Issue 2, Pages 201-206

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.leu.2404467

Keywords

clonality; immunoglobulin (Ig) genes; T-cell receptor; (TCR) genes; PCR; lymphoproliferations; polyclonal

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The diagnosis of malignant lymphoma is a recognized difficult area in histopathology. Therefore, detection of clonality in a suspected lymphoproliferation is a valuable diagnostic criterion. We have developed primer sets for the detection of rearrangements in the B- and T-cell receptor genes as reliable tools for clonality assessment in lymphoproliferations suspected for lymphoma. In this issue of Leukemia, the participants of the BIOMED-2 Concerted Action CT98-3936 report on the validation of the newly developed clonality assays in various disease entities. Clonality was detected in 99% of all B- cell malignancies and in 94% of all T-cell malignancies, whereas the great majority of reactive lesions showed polyclonality. The combined BIOMED-2 results are summarized in a guideline, which can now be implemented in routine lymphoma diagnostics. The use of this standardized approach in patients with a suspect lymphoproliferation will result in improved diagnosis of malignant lymphoma.

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