Intramedullary spinal cord metastasis as initial presentation of systemic cancer--report of a rare case.

Zentralblatt Fur Neurochirurgie Pub Date : 2007-11-01 Epub Date: 2007-10-29 DOI:10.1055/s-2007-985856
C Marquart, M Weckesser, P Schueller, M Hasselblatt, H Wassmann, J Schröder
{"title":"Intramedullary spinal cord metastasis as initial presentation of systemic cancer--report of a rare case.","authors":"C Marquart,&nbsp;M Weckesser,&nbsp;P Schueller,&nbsp;M Hasselblatt,&nbsp;H Wassmann,&nbsp;J Schröder","doi":"10.1055/s-2007-985856","DOIUrl":null,"url":null,"abstract":"<p><p>We report the rare case of a 74-year-old man who was admitted to our hospital with rapid progression of tetraparesis, which was most apparent in the lower right limb, sensory disturbances from C3 to S1 on the left side and recent onset of constipation and urinary retention. There was no known history of cancer. As MRI of the neck disclosed a cervical intramedullary mass lesion at C 4/5 level suspicious for a primary glial tumour, the patient underwent surgery. After microsurgical excision the histological analysis of the lesion unexpectedly revealed an intramedullary spinal cord metastasis (ISCM) of a poorly differentiated carcinoma, immunohistochemically consistent with a bronchial carcinoma. As intramedullary spinal cord metastases are generally associated with poor survival, a palliative irradiation of the levels C1-6 was additionally performed. Unfortunately tetraparesis and numbness remained. The very rare occurrence of intramedullary spinal cord metastasis and the absence of pathognomonic symptoms often lead to a delay until an underlying malignancy is discovered. Although rare, intramedullary spinal cord metastasis should be considered as a differential diagnosis of a spinal intramedullary lesion. Surgery and radiation are both options in the controversially discussed treatment of ISCM.</p>","PeriodicalId":50708,"journal":{"name":"Zentralblatt Fur Neurochirurgie","volume":"68 4","pages":"214-6"},"PeriodicalIF":0.0000,"publicationDate":"2007-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2007-985856","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zentralblatt Fur Neurochirurgie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/s-2007-985856","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2007/10/29 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10

Abstract

We report the rare case of a 74-year-old man who was admitted to our hospital with rapid progression of tetraparesis, which was most apparent in the lower right limb, sensory disturbances from C3 to S1 on the left side and recent onset of constipation and urinary retention. There was no known history of cancer. As MRI of the neck disclosed a cervical intramedullary mass lesion at C 4/5 level suspicious for a primary glial tumour, the patient underwent surgery. After microsurgical excision the histological analysis of the lesion unexpectedly revealed an intramedullary spinal cord metastasis (ISCM) of a poorly differentiated carcinoma, immunohistochemically consistent with a bronchial carcinoma. As intramedullary spinal cord metastases are generally associated with poor survival, a palliative irradiation of the levels C1-6 was additionally performed. Unfortunately tetraparesis and numbness remained. The very rare occurrence of intramedullary spinal cord metastasis and the absence of pathognomonic symptoms often lead to a delay until an underlying malignancy is discovered. Although rare, intramedullary spinal cord metastasis should be considered as a differential diagnosis of a spinal intramedullary lesion. Surgery and radiation are both options in the controversially discussed treatment of ISCM.

髓内脊髓转移是全身性癌症的最初表现——报告一例罕见病例。
我们报告一例罕见的74岁男性患者,他因下肢四肢麻痹的快速进展而入院,最明显的是右下肢,左侧从C3到S1的感觉障碍,最近出现便秘和尿潴留。没有已知的癌症病史。由于颈部MRI显示c4 /5级颈椎髓内肿块,怀疑为原发性神经胶质肿瘤,患者接受了手术。显微手术切除后,病变的组织学分析意外地显示髓内脊髓转移(ISCM)的低分化癌,免疫组织化学一致的支气管癌。由于髓内脊髓转移通常与较差的生存率相关,因此还进行了C1-6水平的姑息性照射。不幸的是,四肢麻痹和麻木仍然存在。脊髓髓内转移的罕见发生和病理症状的缺乏往往导致延迟,直到潜在的恶性肿瘤被发现。尽管罕见,髓内脊髓转移应被视为脊髓髓内病变的鉴别诊断。在有争议的ISCM治疗中,手术和放疗都是两种选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Zentralblatt Fur Neurochirurgie
Zentralblatt Fur Neurochirurgie 医学-神经科学
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信