Primary cauda equina lymphoma confirmed by autopsy: A case report

Author:

Ishizawa Keisuke12ORCID,Komori Takashi2ORCID,Shimazaki Rui3,Nakata Yasuhiro4,Tamaru Jun‐ichi5,Sasaki Atsushi1,Takahashi Kazushi3

Affiliation:

1. Department of Pathology Saitama Medical University Moroyama Japan

2. Department of Laboratory Medicine and Pathology (Neuropathology) Tokyo Metropolitan Neurological Hospital Tokyo Japan

3. Department of Neurology Tokyo Metropolitan Neurological Hospital Tokyo Japan

4. Department of Neuroradiology Tokyo Metropolitan Neurological Hospital Tokyo Japan

5. Department of Pathology, Saitama Medical Center Saitama Medical University Kawagoe Japan

Abstract

Compared with those involving the central nervous system, lymphomas involving the peripheral nervous system, namely neurolymphomatosis, are extremely rare. Neurolymphomatosis is classified as primary or secondary; the former is much rarer than the latter. Herein, we present an autopsied case of primary cauda equina lymphoma (PCEL), a type of primary neurolymphomatosis, with a literature review of autopsied cases of PCEL as well as primary neurolymphomatosis other than PCEL (non‐PCEL primary neurolymphomatosis). A 70‐year‐old woman presented with difficulty walking, followed by paraplegia and then bladder and bowel disturbance. On magnetic resonance imaging, the cauda equina was diffusely enlarged and enhanced with gadolinium. The brainstem and cerebellum were also enhanced with gadolinium along their surface. The differential diagnosis of the patient included meningeal tumors (other than lymphomas), lymphomas, or sarcoidosis. The biopsy of the cauda equina was planned for a definite diagnosis, but because the patient deteriorated so rapidly, it was not performed. Eventually, she was affected by cranial nerve palsies. With the definite diagnosis being undetermined, the patient died approximately 1.5 years after the onset of disesase. At autopsy, the cauda equina was replaced by a bulky mass composed of atypical B‐lymphoid cells, consistent with diffuse large B‐cell lymphoma (DLBCL). The spinal cord was heavily infiltrated, as were the spinal/cranial nerves and subarachnoid space. There was metastasis in the left adrenal. The patient was finally diagnosed postmortem as PCEL with a DLBCL phenotype. To date, there have been a limited number of autopsied cases of PCEL and non‐PCEL primary neurolymphomatosis (nine cases in all, including ours). The diagnosis is, without exception, B‐cell lymphoma including DLBCL, and the histology features central nervous system parenchymal infiltration, nerve root involvement, and subarachnoid dissemination (lymphomatous meningitis). Metastases are not uncommon. All clinicians and pathologists should be aware of lymphomas primarily involving the peripheral nervous system.

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

Reference19 articles.

1. Primary cauda equina lymphoma diagnosed by nerve biopsy: A case report and literature review;Suzuki K;Oncol Lett,2018

2. Solitary sciatic nerve lymphoma as an initial manifestation of diffuse neurolymphomatosis

3. Neurolymphomatosis

4. Neurolymphomatosis: an International Primary CNS Lymphoma Collaborative Group report

5. Lymphoma nerve infiltration;Baehring JM;Eur Assoc Neurooncol Mag,2014

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3