Primary diffuse large B‐cell lymphoma of the central nervous system with rapidly progressing lesions after dimethyl fumarate treatment, showing relapsing and remitting symptoms: A case report

Background We present a case of B‐cell type primary central nervous system lymphoma that rapidly progressed after dimethyl fumarate (DMF) administration. Case presentation An asymptomatic white matter lesion of the left frontal lobe was observed in a 56‐year‐old Japanese man on magnetic resonance im...

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Veröffentlicht in:Clinical & experimental neuroimmunology 2022-02, Vol.13 (1), p.60-65
Hauptverfasser: Kitazaki, Yuki, Ueno, Asako, Maeda, Kenichiro, Asano, Rei, Aoki, Go, Katsuki, Ayumu, Shirafuji, Norimichi, Yamauchi, Takahiro, Isozaki, Makoto, Saida, Takahiko, Nakamoto, Yasunari, Hamano, Tadanori
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container_issue 1
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container_title Clinical & experimental neuroimmunology
container_volume 13
creator Kitazaki, Yuki
Ueno, Asako
Maeda, Kenichiro
Asano, Rei
Aoki, Go
Katsuki, Ayumu
Shirafuji, Norimichi
Yamauchi, Takahiro
Isozaki, Makoto
Saida, Takahiko
Nakamoto, Yasunari
Hamano, Tadanori
description Background We present a case of B‐cell type primary central nervous system lymphoma that rapidly progressed after dimethyl fumarate (DMF) administration. Case presentation An asymptomatic white matter lesion of the left frontal lobe was observed in a 56‐year‐old Japanese man on magnetic resonance imaging during a medical checkup. For the subsequent 5 months, the sporadic white matter lesion showed no change and no contrast effect. He suddenly presented with right upper limb paralysis on day 74. After improvement, he had a recurrence of right upper limb paralysis and diminished vision loss. Based on the 2017 revised McDonald criteria, two attacks, objective clinical evidence of one lesion and cerebrospinal fluid oligoclonal band assay positivity, he was diagnosed with relapsing–remitting multiple sclerosis and administered DMF. Three months after DMF administration, he developed new brain lesions that progressed rapidly; additional immunotherapy was ineffective. He was pathologically diagnosed with B‐cell type primary central nervous system lymphoma using brain biopsy on day 301. Conclusion Patients with rapidly progressing white matter lesions after DMF administration should be suspected for B‐cell type primary central nervous system lymphoma and pathologically diagnosed using brain biopsy. Pathological findings for the right basal ganglia lesion, based on immunostaining with (A) hematoxylin‐eosin, (B) anti‐CD3, (C) anti‐CD20, and (D) anti‐CD5.
doi_str_mv 10.1111/cen3.12656
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Case presentation An asymptomatic white matter lesion of the left frontal lobe was observed in a 56‐year‐old Japanese man on magnetic resonance imaging during a medical checkup. For the subsequent 5 months, the sporadic white matter lesion showed no change and no contrast effect. He suddenly presented with right upper limb paralysis on day 74. After improvement, he had a recurrence of right upper limb paralysis and diminished vision loss. Based on the 2017 revised McDonald criteria, two attacks, objective clinical evidence of one lesion and cerebrospinal fluid oligoclonal band assay positivity, he was diagnosed with relapsing–remitting multiple sclerosis and administered DMF. Three months after DMF administration, he developed new brain lesions that progressed rapidly; additional immunotherapy was ineffective. He was pathologically diagnosed with B‐cell type primary central nervous system lymphoma using brain biopsy on day 301. Conclusion Patients with rapidly progressing white matter lesions after DMF administration should be suspected for B‐cell type primary central nervous system lymphoma and pathologically diagnosed using brain biopsy. Pathological findings for the right basal ganglia lesion, based on immunostaining with (A) hematoxylin‐eosin, (B) anti‐CD3, (C) anti‐CD20, and (D) anti‐CD5.</description><identifier>ISSN: 1759-1961</identifier><identifier>EISSN: 1759-1961</identifier><identifier>DOI: 10.1111/cen3.12656</identifier><language>eng</language><publisher>Ube: Wiley Subscription Services, Inc</publisher><subject>B-cell lymphoma ; Biopsy ; Case reports ; Central nervous system ; Cerebrospinal fluid ; diffuse large B‐cell lymphoma ; dimethyl fumarate ; Frontal lobe ; Immunotherapy ; Lesions ; Lymphoma ; Magnetic resonance imaging ; Multiple sclerosis ; Nervous system ; Neuroimaging ; Paralysis ; primary central nervous system lymphoma ; Substantia alba</subject><ispartof>Clinical &amp; experimental neuroimmunology, 2022-02, Vol.13 (1), p.60-65</ispartof><rights>2021 The Authors. published by John Wiley &amp; Sons Australia, Ltd on behalf of Japanese Society for Neuroimmunology</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). 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Case presentation An asymptomatic white matter lesion of the left frontal lobe was observed in a 56‐year‐old Japanese man on magnetic resonance imaging during a medical checkup. For the subsequent 5 months, the sporadic white matter lesion showed no change and no contrast effect. He suddenly presented with right upper limb paralysis on day 74. After improvement, he had a recurrence of right upper limb paralysis and diminished vision loss. Based on the 2017 revised McDonald criteria, two attacks, objective clinical evidence of one lesion and cerebrospinal fluid oligoclonal band assay positivity, he was diagnosed with relapsing–remitting multiple sclerosis and administered DMF. Three months after DMF administration, he developed new brain lesions that progressed rapidly; additional immunotherapy was ineffective. He was pathologically diagnosed with B‐cell type primary central nervous system lymphoma using brain biopsy on day 301. Conclusion Patients with rapidly progressing white matter lesions after DMF administration should be suspected for B‐cell type primary central nervous system lymphoma and pathologically diagnosed using brain biopsy. Pathological findings for the right basal ganglia lesion, based on immunostaining with (A) hematoxylin‐eosin, (B) anti‐CD3, (C) anti‐CD20, and (D) anti‐CD5.</description><subject>B-cell lymphoma</subject><subject>Biopsy</subject><subject>Case reports</subject><subject>Central nervous system</subject><subject>Cerebrospinal fluid</subject><subject>diffuse large B‐cell lymphoma</subject><subject>dimethyl fumarate</subject><subject>Frontal lobe</subject><subject>Immunotherapy</subject><subject>Lesions</subject><subject>Lymphoma</subject><subject>Magnetic resonance imaging</subject><subject>Multiple sclerosis</subject><subject>Nervous system</subject><subject>Neuroimaging</subject><subject>Paralysis</subject><subject>primary central nervous system lymphoma</subject><subject>Substantia alba</subject><issn>1759-1961</issn><issn>1759-1961</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp9UcFu2zAMNYoVWND2si8g0NuwpJFlW_ZuWZC1A4q1h_ZsyDIVu5AtT5Qb-LZP2C_1V_olVeoddhovJIH3-Ei-KPrE1isW4kphz1csztLsJFowkRZLVmTswz_1x-iC6Gkdgud5IpJF9HLv2k66CepW65EQjHR7hG-vv_8oNAbM1A2N7SRYDb5BCBreSQM9umc7EtBEHjs4tL4BJ4e2NhMMzu4dErX9HgxSa3sCqT26INKhbyYDegyi0iN4h9J3YegXoMYejhSHRg7vZNnXoeta748dhVW87egrbEDJsKrDwTp_Hp1qaQgv_uaz6PH77mF7s7y9u_6x3dwuVczTbKm4qirF8qLIEsESoRnGnKtEpLVQIq0qyQuNldYiloxVWAvN41TzvOJM5zzjZ9HlPDec92tE8uWTHV0fJMs4i8M3Oc9YQH2eUcpZIoe6HOYHl2xdHl0qjy6V7y4FMJvBh9bg9B9kud395DPnDa2kmqc</recordid><startdate>202202</startdate><enddate>202202</enddate><creator>Kitazaki, Yuki</creator><creator>Ueno, Asako</creator><creator>Maeda, Kenichiro</creator><creator>Asano, Rei</creator><creator>Aoki, Go</creator><creator>Katsuki, Ayumu</creator><creator>Shirafuji, Norimichi</creator><creator>Yamauchi, Takahiro</creator><creator>Isozaki, Makoto</creator><creator>Saida, Takahiko</creator><creator>Nakamoto, Yasunari</creator><creator>Hamano, Tadanori</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope></search><sort><creationdate>202202</creationdate><title>Primary diffuse large B‐cell lymphoma of the central nervous system with rapidly progressing lesions after dimethyl fumarate treatment, showing relapsing and remitting symptoms: A case report</title><author>Kitazaki, Yuki ; Ueno, Asako ; Maeda, Kenichiro ; Asano, Rei ; Aoki, Go ; Katsuki, Ayumu ; Shirafuji, Norimichi ; Yamauchi, Takahiro ; Isozaki, Makoto ; Saida, Takahiko ; Nakamoto, Yasunari ; Hamano, Tadanori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2356-c3cbbc1899647147f1e233c475d7c75bba39febff72a11bed7f325f38b31f8363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>B-cell lymphoma</topic><topic>Biopsy</topic><topic>Case reports</topic><topic>Central nervous system</topic><topic>Cerebrospinal fluid</topic><topic>diffuse large B‐cell lymphoma</topic><topic>dimethyl fumarate</topic><topic>Frontal lobe</topic><topic>Immunotherapy</topic><topic>Lesions</topic><topic>Lymphoma</topic><topic>Magnetic resonance imaging</topic><topic>Multiple sclerosis</topic><topic>Nervous system</topic><topic>Neuroimaging</topic><topic>Paralysis</topic><topic>primary central nervous system lymphoma</topic><topic>Substantia alba</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kitazaki, Yuki</creatorcontrib><creatorcontrib>Ueno, Asako</creatorcontrib><creatorcontrib>Maeda, Kenichiro</creatorcontrib><creatorcontrib>Asano, Rei</creatorcontrib><creatorcontrib>Aoki, Go</creatorcontrib><creatorcontrib>Katsuki, Ayumu</creatorcontrib><creatorcontrib>Shirafuji, Norimichi</creatorcontrib><creatorcontrib>Yamauchi, Takahiro</creatorcontrib><creatorcontrib>Isozaki, Makoto</creatorcontrib><creatorcontrib>Saida, Takahiko</creatorcontrib><creatorcontrib>Nakamoto, Yasunari</creatorcontrib><creatorcontrib>Hamano, Tadanori</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><jtitle>Clinical &amp; experimental neuroimmunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kitazaki, Yuki</au><au>Ueno, Asako</au><au>Maeda, Kenichiro</au><au>Asano, Rei</au><au>Aoki, Go</au><au>Katsuki, Ayumu</au><au>Shirafuji, Norimichi</au><au>Yamauchi, Takahiro</au><au>Isozaki, Makoto</au><au>Saida, Takahiko</au><au>Nakamoto, Yasunari</au><au>Hamano, Tadanori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary diffuse large B‐cell lymphoma of the central nervous system with rapidly progressing lesions after dimethyl fumarate treatment, showing relapsing and remitting symptoms: A case report</atitle><jtitle>Clinical &amp; experimental neuroimmunology</jtitle><date>2022-02</date><risdate>2022</risdate><volume>13</volume><issue>1</issue><spage>60</spage><epage>65</epage><pages>60-65</pages><issn>1759-1961</issn><eissn>1759-1961</eissn><abstract>Background We present a case of B‐cell type primary central nervous system lymphoma that rapidly progressed after dimethyl fumarate (DMF) administration. Case presentation An asymptomatic white matter lesion of the left frontal lobe was observed in a 56‐year‐old Japanese man on magnetic resonance imaging during a medical checkup. For the subsequent 5 months, the sporadic white matter lesion showed no change and no contrast effect. He suddenly presented with right upper limb paralysis on day 74. After improvement, he had a recurrence of right upper limb paralysis and diminished vision loss. Based on the 2017 revised McDonald criteria, two attacks, objective clinical evidence of one lesion and cerebrospinal fluid oligoclonal band assay positivity, he was diagnosed with relapsing–remitting multiple sclerosis and administered DMF. Three months after DMF administration, he developed new brain lesions that progressed rapidly; additional immunotherapy was ineffective. He was pathologically diagnosed with B‐cell type primary central nervous system lymphoma using brain biopsy on day 301. Conclusion Patients with rapidly progressing white matter lesions after DMF administration should be suspected for B‐cell type primary central nervous system lymphoma and pathologically diagnosed using brain biopsy. Pathological findings for the right basal ganglia lesion, based on immunostaining with (A) hematoxylin‐eosin, (B) anti‐CD3, (C) anti‐CD20, and (D) anti‐CD5.</abstract><cop>Ube</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/cen3.12656</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects B-cell lymphoma
Biopsy
Case reports
Central nervous system
Cerebrospinal fluid
diffuse large B‐cell lymphoma
dimethyl fumarate
Frontal lobe
Immunotherapy
Lesions
Lymphoma
Magnetic resonance imaging
Multiple sclerosis
Nervous system
Neuroimaging
Paralysis
primary central nervous system lymphoma
Substantia alba
title Primary diffuse large B‐cell lymphoma of the central nervous system with rapidly progressing lesions after dimethyl fumarate treatment, showing relapsing and remitting symptoms: A case report
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