[Waldenström巨球蛋白血症并发神经浸润引起的周围神经病变]。

Natsuki Norioka, Naoki Kurita, Yuya Kamura, Tatsuhiro Sakamoto, Takayasu Kato, Yasuhisa Yokoyama, Hidekazu Nishikii, Naoshi Obara, Mamiko Sakata-Yanagimoto, Hana Takahashi, Kiyotaka Nakamagoe, Akiko Ishii, Ryota Matsuoka, Toru Nanmoku, Akira Tamaoka, Shigeru Chiba
{"title":"[Waldenström巨球蛋白血症并发神经浸润引起的周围神经病变]。","authors":"Natsuki Norioka,&nbsp;Naoki Kurita,&nbsp;Yuya Kamura,&nbsp;Tatsuhiro Sakamoto,&nbsp;Takayasu Kato,&nbsp;Yasuhisa Yokoyama,&nbsp;Hidekazu Nishikii,&nbsp;Naoshi Obara,&nbsp;Mamiko Sakata-Yanagimoto,&nbsp;Hana Takahashi,&nbsp;Kiyotaka Nakamagoe,&nbsp;Akiko Ishii,&nbsp;Ryota Matsuoka,&nbsp;Toru Nanmoku,&nbsp;Akira Tamaoka,&nbsp;Shigeru Chiba","doi":"10.11406/rinketsu.64.18","DOIUrl":null,"url":null,"abstract":"<p><p>A 51-year-old man with the chief complaint of glove- and stocking-type dysesthesia for >3 years was diagnosed with Waldenström's macroglobulinemia (WM) based on IgM-type M-proteinemia, bone marrow infiltration of plasmacytoid B cells, multiple lymphadenopathies, and splenomegaly. A nerve conduction examination suggested demyelinating neuropathy. Serum anti-myelin-associated glycoprotein antibody was negative. Sural nerve biopsy showed myelin thinning, suggesting demyelination. Axonal damage and tumor cell infiltration in the intrafascicular epineurium were also observed. After chemotherapies with rituximab and bendamustine, M-proteinemia and lymphadenopathies disappeared. However, abnormalities in the nerve conduction examination and dysesthesia were only slightly alleviated. As articles describing patients with WM with peripheral nerve infiltration are limited, we report this case with a literature review.</p>","PeriodicalId":6352,"journal":{"name":"[Rinsho ketsueki] The Japanese journal of clinical hematology","volume":"64 1","pages":"18-22"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Waldenström macroglobulinemia complicated by peripheral neuropathy due to neural infiltration].\",\"authors\":\"Natsuki Norioka,&nbsp;Naoki Kurita,&nbsp;Yuya Kamura,&nbsp;Tatsuhiro Sakamoto,&nbsp;Takayasu Kato,&nbsp;Yasuhisa Yokoyama,&nbsp;Hidekazu Nishikii,&nbsp;Naoshi Obara,&nbsp;Mamiko Sakata-Yanagimoto,&nbsp;Hana Takahashi,&nbsp;Kiyotaka Nakamagoe,&nbsp;Akiko Ishii,&nbsp;Ryota Matsuoka,&nbsp;Toru Nanmoku,&nbsp;Akira Tamaoka,&nbsp;Shigeru Chiba\",\"doi\":\"10.11406/rinketsu.64.18\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A 51-year-old man with the chief complaint of glove- and stocking-type dysesthesia for >3 years was diagnosed with Waldenström's macroglobulinemia (WM) based on IgM-type M-proteinemia, bone marrow infiltration of plasmacytoid B cells, multiple lymphadenopathies, and splenomegaly. A nerve conduction examination suggested demyelinating neuropathy. Serum anti-myelin-associated glycoprotein antibody was negative. Sural nerve biopsy showed myelin thinning, suggesting demyelination. Axonal damage and tumor cell infiltration in the intrafascicular epineurium were also observed. After chemotherapies with rituximab and bendamustine, M-proteinemia and lymphadenopathies disappeared. However, abnormalities in the nerve conduction examination and dysesthesia were only slightly alleviated. As articles describing patients with WM with peripheral nerve infiltration are limited, we report this case with a literature review.</p>\",\"PeriodicalId\":6352,\"journal\":{\"name\":\"[Rinsho ketsueki] The Japanese journal of clinical hematology\",\"volume\":\"64 1\",\"pages\":\"18-22\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"[Rinsho ketsueki] The Japanese journal of clinical hematology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.11406/rinketsu.64.18\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"[Rinsho ketsueki] The Japanese journal of clinical hematology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11406/rinketsu.64.18","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

51岁男性,主诉为手套型和长袜型感觉障碍>3年,基于igm型m蛋白血症、骨髓浆细胞样B细胞浸润、多发性淋巴结病变和脾肿大,诊断为Waldenström大球蛋白血症(WM)。神经传导检查提示脱髓鞘神经病。血清抗髓磷脂相关糖蛋白抗体阴性。腓肠神经活检显示髓鞘变薄,提示脱髓鞘。同时观察到束内神经外膜轴突损伤和肿瘤细胞浸润。经利妥昔单抗和苯达莫司汀化疗后,m蛋白血症和淋巴结病消失。然而,神经传导检查异常和感觉不良仅轻微减轻。由于描述WM伴周围神经浸润的文章有限,我们通过文献回顾来报道这一病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[Waldenström macroglobulinemia complicated by peripheral neuropathy due to neural infiltration].

A 51-year-old man with the chief complaint of glove- and stocking-type dysesthesia for >3 years was diagnosed with Waldenström's macroglobulinemia (WM) based on IgM-type M-proteinemia, bone marrow infiltration of plasmacytoid B cells, multiple lymphadenopathies, and splenomegaly. A nerve conduction examination suggested demyelinating neuropathy. Serum anti-myelin-associated glycoprotein antibody was negative. Sural nerve biopsy showed myelin thinning, suggesting demyelination. Axonal damage and tumor cell infiltration in the intrafascicular epineurium were also observed. After chemotherapies with rituximab and bendamustine, M-proteinemia and lymphadenopathies disappeared. However, abnormalities in the nerve conduction examination and dysesthesia were only slightly alleviated. As articles describing patients with WM with peripheral nerve infiltration are limited, we report this case with a literature review.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
[Refractory esophageal stricture of esophageal mucous membrane pemphigoid after allogeneic hematopoietic stem cell transplantation]. [Successful delivery using interferon α for molecular relapse of chronic myeloid leukemia after interruption of tyrosine kinase inhibitor]. [Diffuse large B-cell lymphoma complicated with pancreatic fistula and peritonitis following initial chemotherapy]. [Autoimmune coagulation factor V/5 deficiency during chronic disseminated intravascular coagulation]. [Analysis of anti-SARS-CoV-2 IgG antibody titers after mRNA booster vaccination in patients with nonmalignant hematological disorders].
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1