• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

腰骶丛神经淋巴瘤病:一种典型的 18FDG PET/CT 表现。

Lumbosacral Plexus Neurolymphomatosis: A Typical 18FDG PET/CT Pattern to Recognize.

机构信息

From the Departments of Nuclear Medicine.

Medical Oncology, Institut Régional du Cancer de Montpellier, Université de Montpellier.

出版信息

Clin Nucl Med. 2022 Apr 1;47(4):352-353. doi: 10.1097/RLU.0000000000003949.

DOI:10.1097/RLU.0000000000003949
PMID:34739401
Abstract

A 79-year-old man anteriorly treated for primary central nervous system diffuse large B-cell lymphoma with MRI complete response after immunochemotherapy was referred 1 year later for 18FDG PET/CT because of right persistent lombosciatic radicular pain for 6 months with negative medullary and spine MRI and negative cerebrospinal fluid cytology. Linearly intense uptake was observed in several roots of lumbosacral plexus, highly suggestive of peripheral neurolymphomatosis relapse. No specific treatment was engaged because of rapid decrease of performance status leading to death.

摘要

一位 79 岁男性,先前因原发性中枢神经系统弥漫性大 B 细胞淋巴瘤接受了免疫化疗,治疗后 MRI 完全缓解。1 年后,因持续 6 个月的右侧腰骶神经根痛而就诊,脊髓和脊柱 MRI 及脑脊液细胞学检查均为阴性。18FDG PET/CT 显示腰骶丛多个神经根线性摄取增强,强烈提示外周神经淋巴组织肿瘤复发。由于患者的功能状态迅速下降导致死亡,因此未进行特定治疗。

相似文献

1
Lumbosacral Plexus Neurolymphomatosis: A Typical 18FDG PET/CT Pattern to Recognize.腰骶丛神经淋巴瘤病:一种典型的 18FDG PET/CT 表现。
Clin Nucl Med. 2022 Apr 1;47(4):352-353. doi: 10.1097/RLU.0000000000003949.
2
Diffuse Large B-Cell Lymphoma Recurring as Neurolymphomatosis on FDG PET/CT.弥漫性大 B 细胞淋巴瘤在 FDG PET/CT 上复发为神经淋巴瘤病。
Clin Nucl Med. 2019 Feb;44(2):145-147. doi: 10.1097/RLU.0000000000002388.
3
Neurolymphomatosis as a late relapse of non-Hodgkin's lymphoma detected by 18F-FDG PET/CT: a case report.18F-FDG PET/CT检测到神经淋巴瘤病作为非霍奇金淋巴瘤的晚期复发:一例报告
Rev Esp Med Nucl Imagen Mol. 2014 Jan-Feb;33(1):39-42. doi: 10.1016/j.remn.2013.03.004. Epub 2013 May 15.
4
Brachial and sacral plexus neurolymphomatosis - unusual regions for disease relapses.臂丛和骶丛神经淋巴瘤病——疾病复发的不寻常部位。
Arq Neuropsiquiatr. 2019 Nov;77(11):832-833. doi: 10.1590/0004-282X20190104.
5
PET-CT imaging of combined brachial and lumbosacral neurolymphomatosis.臂丛和腰骶部神经淋巴瘤病的PET-CT成像
Eur J Haematol. 2005 Jan;74(1):66-9. doi: 10.1111/j.1600-0609.2004.00369.x.
6
Recurrence of nasal type NK/T cell lymphoma presenting as neurolymphomatosis on 18F-FDG PET/CT: A case report and literature review.18F-FDG PET/CT表现为神经淋巴瘤病的鼻型NK/T细胞淋巴瘤复发:1例报告及文献复习
Medicine (Baltimore). 2020 Jan;99(1):e18640. doi: 10.1097/MD.0000000000018640.
7
Neurolymphomatosis of the lumbosacral plexus and its branches: case series and literature review.腰骶丛及其分支神经淋巴瘤病:病例系列和文献复习。
BMC Cancer. 2019 Nov 27;19(1):1149. doi: 10.1186/s12885-019-6365-y.
8
Sciatic and median nerve neurolymphomatosis as initial presentation of B-cell lymphoma.坐骨神经和正中神经神经淋巴瘤病作为 B 细胞淋巴瘤的初始表现。
Radiologia (Engl Ed). 2022 May-Jun;64(3):266-269. doi: 10.1016/j.rxeng.2020.10.003.
9
F-FDG PET/CT imaging findings of extensive neurolymphomatosis as a relapse of diffuse large B cell lymphoma.作为弥漫性大B细胞淋巴瘤复发的广泛性神经淋巴瘤病的F-FDG PET/CT影像学表现
Diagn Interv Imaging. 2019 Sep;100(9):527-528. doi: 10.1016/j.diii.2019.02.006. Epub 2019 Mar 8.
10
Magnetic resonance imaging and F-fluorodeoxyglucose positron emission tomography/computed tomography findings in neurolymphomatosis: an uncommon presentation of diffuse large B cell lymphoma.神经淋巴瘤病的磁共振成像及氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描结果:弥漫性大B细胞淋巴瘤的一种罕见表现
Ann Hematol. 2020 Jan;99(1):203-205. doi: 10.1007/s00277-019-03850-4. Epub 2019 Nov 25.

引用本文的文献

1
A Case Series of Neurolymphomatosis: Role of Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography Scan Reiterated.神经淋巴瘤病例系列:重申氟脱氧葡萄糖正电子发射断层扫描-计算机断层扫描的作用
Indian J Nucl Med. 2023 Jan-Mar;38(1):44-49. doi: 10.4103/ijnm.ijnm_165_22. Epub 2023 Feb 24.