IGH amplification in patients with B cell lymphoma unclassifiable, with features intermediate between diffuse large B cell lymphoma and Burkitt's lymphoma.

Autor: Bellone M; Department of Pathology, Stony Brook University Medical Center, Stony Brook, NY 11794, USA., Zaslav AL; Cytogenetics, Department of Pathology, Stony Brook University Medical Center, Stony Brook, NY 11794, USA., Ahmed T; Department of Pathology, Stony Brook University Medical Center, Stony Brook, NY 11794, USA., Lee HL; Cytogenetics, Department of Pathology, Stony Brook University Medical Center, Stony Brook, NY 11794, USA., Ma Y; Department of Pathology, Stony Brook University Medical Center, Stony Brook, NY 11794, USA., Hu Y; Department of Pathology, Stony Brook University Medical Center, Stony Brook, NY 11794, USA.
Jazyk: angličtina
Zdroj: Biomarker research [Biomark Res] 2014 May 09; Vol. 2, pp. 9. Date of Electronic Publication: 2014 May 09 (Print Publication: 2014).
DOI: 10.1186/2050-7771-2-9
Abstrakt: B cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma (DLBCL) and Burkitt's lymphoma (BL) (B-UNC/BL/DLBCL) is a new category of tumors that have features resembling both DLBCL and BL. These tumors have large and medium sized cells with greater irregularity of nuclei and more prominent nucleoli than BL. Approximately 35% to 50% have C-MYC rearrangements, although half are non-immunoglobulin variants. We identified six cases of B-UNC/BL/DLBCL with low-level IGH amplification. Four patients died with a median survival of 7 months (range, 6-20). In conclusion, to our knowledge low-level IGH amplification has not been previously described and should be evaluated for in this patient population.
Databáze: MEDLINE