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...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Tianqi, Jia, Qingge, Wang, Yingmei, Liu, Yixiong, Han, Donghui, Li, Peifeng, Ma, Jing, Fan, Linni, Yan, Qingguo, Guo, Shuangping, Li, Mingyang, Wang, Zhe
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