Cargando…
Clinicopathological analysis of diffuse large B-cell lymphoma lacking surface immunoglobulin light chain restriction on flow cytometry
Although diffuse large B-cell lymphoma (DLBCL) occasionally lacks surface immunoglobulin light chain restriction (iLCR) on flow cytometry (FCM), little evidence is available for iLCR-negative DLBCL. We retrospectively compared clinicopathological features of iLCR-positive and iLCR-negative DLBCL dia...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JSLRT
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010494/ https://www.ncbi.nlm.nih.gov/pubmed/34707034 http://dx.doi.org/10.3960/jslrt.21017 |
_version_ | 1784687488226295808 |
---|---|
author | Nakaya, Yosuke Sakaida, Miho Yoshida, Masahiro Shimizu, Katsujun Yagi, Naoko Tsutsumi, Minako Yoshimura, Takuro Hayashi, Yoshiki Nakao, Takafumi Inoue, Takeshi Yamane, Takahisa |
author_facet | Nakaya, Yosuke Sakaida, Miho Yoshida, Masahiro Shimizu, Katsujun Yagi, Naoko Tsutsumi, Minako Yoshimura, Takuro Hayashi, Yoshiki Nakao, Takafumi Inoue, Takeshi Yamane, Takahisa |
author_sort | Nakaya, Yosuke |
collection | PubMed |
description | Although diffuse large B-cell lymphoma (DLBCL) occasionally lacks surface immunoglobulin light chain restriction (iLCR) on flow cytometry (FCM), little evidence is available for iLCR-negative DLBCL. We retrospectively compared clinicopathological features of iLCR-positive and iLCR-negative DLBCL diagnosed at our institute between April 2007 and March 2018. iLCR-positive was defined as a κ/λ ratio less than 0.5 or greater than 3 in the gated population on dual-color FCM, and iLCR-negative as other values. Of 81 DLBCL cases with available immunophenotyping by FCM, 63 iLCR-positive DLBCL (78%) and 18 iLCR-negative DLBCL (22%) cases were identified. Survival outcomes of patients with iLCR-negative DLBCL were comparable with those of patients with iLCR-positive DLBCL. Pathological analysis revealed no significant difference except for the lower expression of BCL6 in iLCR-negative DLBCL (12.5% vs 65.5%, p < 0.001), although there was a slightly higher frequency of necrosis (47.1% vs 20.7%, p = 0.058) and lower expression of CD10 (11.8% vs 35.0%, p = 0.078) in iLCR-negative DLBCL than in iLCR-positive DLBCL. The underlying mechanism remains unclear; however, low expression of germinal center markers and tumor necrosis may be associated with the loss of iLCR in DLBCL. |
format | Online Article Text |
id | pubmed-9010494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | JSLRT |
record_format | MEDLINE/PubMed |
spelling | pubmed-90104942022-05-04 Clinicopathological analysis of diffuse large B-cell lymphoma lacking surface immunoglobulin light chain restriction on flow cytometry Nakaya, Yosuke Sakaida, Miho Yoshida, Masahiro Shimizu, Katsujun Yagi, Naoko Tsutsumi, Minako Yoshimura, Takuro Hayashi, Yoshiki Nakao, Takafumi Inoue, Takeshi Yamane, Takahisa J Clin Exp Hematop Original Article Although diffuse large B-cell lymphoma (DLBCL) occasionally lacks surface immunoglobulin light chain restriction (iLCR) on flow cytometry (FCM), little evidence is available for iLCR-negative DLBCL. We retrospectively compared clinicopathological features of iLCR-positive and iLCR-negative DLBCL diagnosed at our institute between April 2007 and March 2018. iLCR-positive was defined as a κ/λ ratio less than 0.5 or greater than 3 in the gated population on dual-color FCM, and iLCR-negative as other values. Of 81 DLBCL cases with available immunophenotyping by FCM, 63 iLCR-positive DLBCL (78%) and 18 iLCR-negative DLBCL (22%) cases were identified. Survival outcomes of patients with iLCR-negative DLBCL were comparable with those of patients with iLCR-positive DLBCL. Pathological analysis revealed no significant difference except for the lower expression of BCL6 in iLCR-negative DLBCL (12.5% vs 65.5%, p < 0.001), although there was a slightly higher frequency of necrosis (47.1% vs 20.7%, p = 0.058) and lower expression of CD10 (11.8% vs 35.0%, p = 0.078) in iLCR-negative DLBCL than in iLCR-positive DLBCL. The underlying mechanism remains unclear; however, low expression of germinal center markers and tumor necrosis may be associated with the loss of iLCR in DLBCL. JSLRT 2021-10-26 /pmc/articles/PMC9010494/ /pubmed/34707034 http://dx.doi.org/10.3960/jslrt.21017 Text en © 2021 by The Japanese Society for Lymphoreticular Tissue Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution ShareAlike (CC BY-NC-SA) 4.0 License. |
spellingShingle | Original Article Nakaya, Yosuke Sakaida, Miho Yoshida, Masahiro Shimizu, Katsujun Yagi, Naoko Tsutsumi, Minako Yoshimura, Takuro Hayashi, Yoshiki Nakao, Takafumi Inoue, Takeshi Yamane, Takahisa Clinicopathological analysis of diffuse large B-cell lymphoma lacking surface immunoglobulin light chain restriction on flow cytometry |
title | Clinicopathological analysis of diffuse large B-cell lymphoma lacking surface immunoglobulin light chain restriction on flow cytometry |
title_full | Clinicopathological analysis of diffuse large B-cell lymphoma lacking surface immunoglobulin light chain restriction on flow cytometry |
title_fullStr | Clinicopathological analysis of diffuse large B-cell lymphoma lacking surface immunoglobulin light chain restriction on flow cytometry |
title_full_unstemmed | Clinicopathological analysis of diffuse large B-cell lymphoma lacking surface immunoglobulin light chain restriction on flow cytometry |
title_short | Clinicopathological analysis of diffuse large B-cell lymphoma lacking surface immunoglobulin light chain restriction on flow cytometry |
title_sort | clinicopathological analysis of diffuse large b-cell lymphoma lacking surface immunoglobulin light chain restriction on flow cytometry |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010494/ https://www.ncbi.nlm.nih.gov/pubmed/34707034 http://dx.doi.org/10.3960/jslrt.21017 |
work_keys_str_mv | AT nakayayosuke clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry AT sakaidamiho clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry AT yoshidamasahiro clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry AT shimizukatsujun clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry AT yaginaoko clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry AT tsutsumiminako clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry AT yoshimuratakuro clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry AT hayashiyoshiki clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry AT nakaotakafumi clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry AT inouetakeshi clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry AT yamanetakahisa clinicopathologicalanalysisofdiffuselargebcelllymphomalackingsurfaceimmunoglobulinlightchainrestrictiononflowcytometry |