Articles

P4.02 BCR-ABL1 kinase domain mutation analysis by next generation sequencing: comparison of Ion Torrent PGM and MiSeq platforms

BJH - volume 7, issue Abstract Book BHS, january 2016

F. Nollet PhD, MSc, P. Vannuffel PhD, C. De Rop , S. Vermeire , D. David , B. Cauwelier MD, PhD

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P3.01 NGS based HLA-genotyping using 2 reagent kits (Omixon, GenDx) and 3 software applications: NGSengine, Twin and SeqNext-HLA

BJH - volume 7, issue Abstract Book BHS, january 2016

B. Cauwelier MD, PhD, S. Vermeire , W. Rosseel , F. Nollet PhD, MSc

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PP4.1 Mutation frequency of SETBP1, ASXL1 and CSF3R in myeloid malignancies: retrospective analysis of 123 patients

BJH - volume 7, issue Abstract Book BHS, january 2016

M. Criel , S. Vermeire , B. Cauwelier MD, PhD, F. Nollet PhD, MSc

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PP1.1 Evaluation of Next Generation Sequencing based clonality analysis of TRG gene rearrangements

BJH - volume 7, issue Abstract Book BHS, january 2016

B. Cauwelier MD, PhD, S. Vermeire , E. Maelbrancke , K. Vanhouteghem PharmD, F. Nollet PhD, MSc

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P2.07 MPN with JAK2 V617F mutation and identical del20q11.2 in three first-degree relatives without identified germline defect

BJH - volume 6, issue Abstract Book BHS, january 2015

J. Dauw , E. Boone PhD, N. Cardinaels MD, E. Moureau , A. Nijs , F. Nollet PhD, MSc, V. Van Hende MD, N. Van Roy PhD, K. Van Eygen MD

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Biclonal biphenotypic B-cell lymphocytosis: a CLL in disguise?

BJH - volume 5, issue 4, december 2014

B. Depreter PhD, PharmD, E. Dumoulin PharmD, J. Billiet MD, B. Cauwelier MD, PhD, B. Maes MD, PhD, C. Matthys MD, J. Van Droogenbroeck MD, F. Nollet PhD, MSc, J. Emmerechts MD, PhD

Summary

We report a rare case of biclonal biphenotypic B-cell lymphocytosis with chronic lymphocytic leukaemia phenotype. Clonality was initially misjudged by immunophenotyping because of its polyphenotypic pattern. Polymerase chain reaction analysis revealed clonality of the immunoglobulin heavy chain and kappa light chain gene rearrangement, indicating the presence of a monoclonal B-lymphocyte population. Immunophenotyping was repeated after cell sorting and revealed two CD5+CD19+ populations with different light chain restriction. Different genetic abnormalities for both clones, as evidenced by fluorescence in situ hybridisation and hypermutation analysis, support the diagnosis of two independently originated but co-existing B-cell clones. This case illustrates the importance of using multiple techniques in the diagnostic work-up of haematological malignancies.

(BELG J HEMATOL 2014;5(4):143–7)

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P2.02 The value of SOX11 overexpression in the differential diagnosis of mantle cell lymphoma

BJH - volume 5, issue Abstract Book BHS, january 2014

B. Depreter PhD, PharmD, F. Nollet PhD, MSc, S. Vermeire , B. Cauwelier MD, PhD, A. Van Hoof MD, PhD, J. Billiet MD

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