Immunoglobulin rearrangement analysis from multiple lesions in the same patient using next-generation sequencing

• Published in: Histopathology 2015-12, Vol.67 (6), p.843-858
• Main Authors: Appenzeller, Silke, Gilissen, Christian, Rijntjes, Jos, Tops, Bastiaan B J, Kastner-van Raaij, Annemiek, Hebeda, Konnie M, Nissen, Loes, Dutilh, Bas E, van Krieken, J Han J M, Groenen, Patricia J T A
• Format: Article
• Language: English
• Subjects: Colitis, Ulcerative - complications; Colitis, Ulcerative - genetics; Colitis, Ulcerative - pathology; Epstein-Barr virus; Female; High-Throughput Nucleotide Sequencing; Humans; Immunoglobulin Heavy Chains - genetics; immunoglobulin rearrangement; Immunoglobulins; Ion Torrent-PGM; Lymphoma; Lymphoma - complications; Lymphoma - genetics; Lymphoma - pathology; Lymphoproliferative Disorders - complications; Lymphoproliferative Disorders - genetics; Lymphoproliferative Disorders - pathology; Middle Aged; molecular pathology; Patients; ulcerative colitis; Young Adult
• ISSN: 0309-0167; 1365-2559
• DOI: 10.1111/his.12714

Aims For patients who have multiple lymphomas with discordant pathology, it is relevant to determine whether there is one disseminated lymphoma or two unrelated lymphomas. Patients with disseminated, clonally related lymphomas are usually treated with the most powerful drugs available, while patients with unrelated (primary) lymphomas receive mainly standard first‐line therapies. Methods and results We used next‐generation sequencing on the Ion Torrent Personal Genome Machine to characterize the immunoglobulin heavy gene V–D–J rearrangements in two diagnostic tissue samples, including formalin‐fixed and paraffin‐embedded tissue, of two patients with iatrogenic immunodeficiency‐associated Epstein–Barr virus lymphoproliferative disorder, with ulcerative colitis as underlying disease. The immunoglobulin rearrangement sequences obtained by next‐generation sequencing revealed undoubtedly clonally related lesions in two tissue biopsies that were taken over time in the first patient, which is concordant with disseminated lymphoma. The other patient showed two clonally unrelated lesions, which is incompatible with clonal dissemination. This information was not inferred from evaluation of the heavy and light chain rearrangements by fragment analysis, which is currently the gold standard. Conclusion Our study demonstrates the diagnostic application of next‐generation sequencing of immunoglobulin rearrangement assessment in pathology for clinical decision‐making in patients with several simultaneous or subsequent lymphoproliferations.