| Literature DB >> 25612555 |
Raul Cordoba1, Beatriz Alvarez2, Pilar Masso3, Fernando Ataulfo Gonzalez4, Luz Conejo2, Diego Velasco4, Juan-Manuel Alonso4, Jesus Villarrubia4, Fernando Cava4, Pilar Llamas1.
Abstract
Double-hit lymphoma (DHL) is a rare type of lymphoma with concurrent chromosomal translocations of C-MYC with BCL2 or BCL6, associated with unfavorable prognosis. We describe a case of DHL in a 79-year-old female patient previously diagnosed with diffuse large B-cell lymphoma (DLBCL) with an early relapse in the ascitic fluid. A seven-color multiparametric flow cytometry immunophenotyping study of the ascitic fluid was carried out, and revealed 99.78% of large in size and high cellular complexity B-cells positive for CD19, CD10 (64.27%), CD45 dim, CD22 dim, CD25 (60%), CD43 bright, CD38 bright, and IgM (18.53%); and negative for CD20, CD5, CD23, CD79b, CD103, CD200, CD11c, and FMC7, and 78.99% without light chain expression and 21% with Lambda chain restriction. Due to the expression of CD19 and CD10 with overexpression of BCL-2 protein and due to CD43 and CD38 positivity detected, those cells showed features between DLBCL and Burkitt lymphoma. Fluorescence in situ hybridization (FISH) confirmed both c-MYC/IGH and BCL2/IGH rearrangement. Our findings may help to identify cases requiring additional cytogenetic analysis.Entities:
Keywords: double-hit; flow cytometry; lymphoma
Mesh:
Year: 2015 PMID: 25612555 DOI: 10.1002/cyto.b.21227
Source DB: PubMed Journal: Cytometry B Clin Cytom ISSN: 1552-4949 Impact factor: 3.058