Cargando…
Rare cases of primary central nervous system anaplastic variant of diffuse large B-cell lymphoma
BACKGROUND: Primary central nervous system (CNS) diffuse large B-cell lymphoma (DLBCL) is a rare intracranial tumor, defined as DLBCL arising from the brain, spinal cord, leptomeninges and eye, with an overall annual incidence of 5 cases per million. The primary CNS anaplastic variant of DLBCL (A-DL...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528307/ https://www.ncbi.nlm.nih.gov/pubmed/31109360 http://dx.doi.org/10.1186/s13000-019-0826-0 |
_version_ | 1783420188880797696 |
---|---|
author | Xu, Tianqi Jia, Qingge Wang, Yingmei Liu, Yixiong Han, Donghui Li, Peifeng Ma, Jing Fan, Linni Yan, Qingguo Guo, Shuangping Li, Mingyang Wang, Zhe |
author_facet | Xu, Tianqi Jia, Qingge Wang, Yingmei Liu, Yixiong Han, Donghui Li, Peifeng Ma, Jing Fan, Linni Yan, Qingguo Guo, Shuangping Li, Mingyang Wang, Zhe |
author_sort | Xu, Tianqi |
collection | PubMed |
description | BACKGROUND: Primary central nervous system (CNS) diffuse large B-cell lymphoma (DLBCL) is a rare intracranial tumor, defined as DLBCL arising from the brain, spinal cord, leptomeninges and eye, with an overall annual incidence of 5 cases per million. The primary CNS anaplastic variant of DLBCL (A-DLBCL) is even less common; to our knowledge, there are only two other case reports in the literature. The aim of this report is to present rare cases of primary CNS A-DLBCL and study their clinicopathologic and genetic features. CASE PRESENTATION: We report 3 patients, two men and one woman, aged 54, 55 and 67 years old, with primary CNS A-DLBCL. All 3 patients had a high International Extranodal Lymphoma Study Group (IELSG) score; although the patients were treated with methotrexate-based regimens and/or with radiation therapy, the overall survival was only 2, 5, and 8 months. All 3 patients presented with characteristic features of perivascular space infiltration with bizarre-shaped tumor cells, leading to the diagnosis of primary CNS A-DLBCL. Concurrent of MYC and BCL2 and/or BCL6 abnormalities and MYC/BCL2 double-expressor DLBCL occurred in all 3 patients; two patients had MYC/BCL2/BCL6 triple extra copies, and one patient had MYC extra copy and BCL6 translocation. All 3 patients displayed mutations in MYD88 L265P and nuclear positivity for RELA, RELB and/or c-Rel, indicating constitutive activation of the NF-κB pathway. CONCLUSIONS: These cases shed light on the unique genetic alterations and biological features of primary CNS A-DLBCL. Patients with primary CNS A-DLBCL may often have a MYC/BCL2 double-expressor and concurrent MYC and BCL2 and/or BCL6 genetic abnormalities, as well as constitutive activation of the NF-κB pathway. Primary CNS A-DLBCL follows a very aggressive disease course and poor prognosis. In the future, a large number of cases should be analyzed, and the evaluation of molecular genetic characteristics could help with practical and therapeutic implications for primary CNS A-DLBCL. |
format | Online Article Text |
id | pubmed-6528307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65283072019-05-28 Rare cases of primary central nervous system anaplastic variant of diffuse large B-cell lymphoma Xu, Tianqi Jia, Qingge Wang, Yingmei Liu, Yixiong Han, Donghui Li, Peifeng Ma, Jing Fan, Linni Yan, Qingguo Guo, Shuangping Li, Mingyang Wang, Zhe Diagn Pathol Case Report BACKGROUND: Primary central nervous system (CNS) diffuse large B-cell lymphoma (DLBCL) is a rare intracranial tumor, defined as DLBCL arising from the brain, spinal cord, leptomeninges and eye, with an overall annual incidence of 5 cases per million. The primary CNS anaplastic variant of DLBCL (A-DLBCL) is even less common; to our knowledge, there are only two other case reports in the literature. The aim of this report is to present rare cases of primary CNS A-DLBCL and study their clinicopathologic and genetic features. CASE PRESENTATION: We report 3 patients, two men and one woman, aged 54, 55 and 67 years old, with primary CNS A-DLBCL. All 3 patients had a high International Extranodal Lymphoma Study Group (IELSG) score; although the patients were treated with methotrexate-based regimens and/or with radiation therapy, the overall survival was only 2, 5, and 8 months. All 3 patients presented with characteristic features of perivascular space infiltration with bizarre-shaped tumor cells, leading to the diagnosis of primary CNS A-DLBCL. Concurrent of MYC and BCL2 and/or BCL6 abnormalities and MYC/BCL2 double-expressor DLBCL occurred in all 3 patients; two patients had MYC/BCL2/BCL6 triple extra copies, and one patient had MYC extra copy and BCL6 translocation. All 3 patients displayed mutations in MYD88 L265P and nuclear positivity for RELA, RELB and/or c-Rel, indicating constitutive activation of the NF-κB pathway. CONCLUSIONS: These cases shed light on the unique genetic alterations and biological features of primary CNS A-DLBCL. Patients with primary CNS A-DLBCL may often have a MYC/BCL2 double-expressor and concurrent MYC and BCL2 and/or BCL6 genetic abnormalities, as well as constitutive activation of the NF-κB pathway. Primary CNS A-DLBCL follows a very aggressive disease course and poor prognosis. In the future, a large number of cases should be analyzed, and the evaluation of molecular genetic characteristics could help with practical and therapeutic implications for primary CNS A-DLBCL. BioMed Central 2019-05-20 /pmc/articles/PMC6528307/ /pubmed/31109360 http://dx.doi.org/10.1186/s13000-019-0826-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Xu, Tianqi Jia, Qingge Wang, Yingmei Liu, Yixiong Han, Donghui Li, Peifeng Ma, Jing Fan, Linni Yan, Qingguo Guo, Shuangping Li, Mingyang Wang, Zhe Rare cases of primary central nervous system anaplastic variant of diffuse large B-cell lymphoma |
title | Rare cases of primary central nervous system anaplastic variant of diffuse large B-cell lymphoma |
title_full | Rare cases of primary central nervous system anaplastic variant of diffuse large B-cell lymphoma |
title_fullStr | Rare cases of primary central nervous system anaplastic variant of diffuse large B-cell lymphoma |
title_full_unstemmed | Rare cases of primary central nervous system anaplastic variant of diffuse large B-cell lymphoma |
title_short | Rare cases of primary central nervous system anaplastic variant of diffuse large B-cell lymphoma |
title_sort | rare cases of primary central nervous system anaplastic variant of diffuse large b-cell lymphoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528307/ https://www.ncbi.nlm.nih.gov/pubmed/31109360 http://dx.doi.org/10.1186/s13000-019-0826-0 |
work_keys_str_mv | AT xutianqi rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT jiaqingge rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT wangyingmei rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT liuyixiong rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT handonghui rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT lipeifeng rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT majing rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT fanlinni rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT yanqingguo rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT guoshuangping rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT limingyang rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma AT wangzhe rarecasesofprimarycentralnervoussystemanaplasticvariantofdiffuselargebcelllymphoma |