Mature B-cell acute lymphoblastic leukemia (ALL) is typically associated with the FAB-L3 morphology and rearrangement of the MYC gene, features characteristic of the leukemic phase of Burkitt's lymphoma. However, the term 'mature' has also been used to describe other rare cases of B-ALL with light-chain surface immunoglobulin expression. In contrast, infantile B-cell ALL is generally characterized by rearrangement of the MLL gene, an immature pro-B-cell phenotype, and CD10 negativity. We describe two unusual cases of infantile B-ALL with non-L3 morphology, expressing a mature B-cell phenotype (λ slg+, CD19+, CD10-, TdT-, and CD34-), and showing MLL rearrangement without MYC rearrangement at presentation. Both infants relapsed after months of morphologic and genetic remission. At relapse, the t(9;11) translocation was detected in both cases by spectral karyotyping. After the initial relapse, both cases followed a rapid and aggressive course. Literature search identified few similar cases, all expressed λ surface immunoglobulin and showed MLL rearrangement (majority with the t(9; 11) translocation). These cases show that B-ALL with MLL rearrangement, especially the t(9;11) translocation, can express a 'mature' B-cell phenotype and may represent a distinct subset. Identification of additional cases will further clarify the significance of MLL rearrangements in mature B-ALL.
CITATION STYLE
Tsao, L., Draoua, H. Y., Osunkwo, I., Nandula, S. V., Murty, V. V. S., Mansukhani, M., … Alobeid, B. (2004). Mature B-cell acute lymphoblastic leukemia with t(91;11) translocation: A distinct subset of B-cell acute lymphloblastic leukemia. Modern Pathology, 17(7), 832–839. https://doi.org/10.1038/modpathol.3800128
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