原发性硬脑膜淋巴瘤模拟En斑块脑桥小脑角脑膜瘤。

IF 0.7 Q4 PATHOLOGY
Case Reports in Pathology Pub Date : 2021-07-23 eCollection Date: 2021-01-01 DOI:10.1155/2021/2845995
Mei Xu, Ashish Bains, Yuan Rong
{"title":"原发性硬脑膜淋巴瘤模拟En斑块脑桥小脑角脑膜瘤。","authors":"Mei Xu,&nbsp;Ashish Bains,&nbsp;Yuan Rong","doi":"10.1155/2021/2845995","DOIUrl":null,"url":null,"abstract":"<p><p>Primary dural lymphoma (PDL) usually arises from the calvarial dura without the brain parenchyma or systemic involvement and thus may not be considered as a typical form of primary CNS lymphoma (PCNSL). It is exceedingly rare. When it occurs, it might not be suspected as a primary diagnosis on clinical and radiologic findings. We present a PDL case that occurs at the cerebellopontine (CP) angle mimicking en plaque meningioma. The tumor histopathology showed a lymphoproliferative disorder immunophenotypically consistent with a low-grade marginal zone lymphoma. Bone marrow and systemic involvements were not identified, and a diagnosis of PDL was established. As a residual tumor at the CP angle was inaccessible to surgery, postoperative radiation therapy was performed. No recurrence was found at 15-month follow-up. PDLs are mostly indolent and have a good prognosis. There is no doubt that the most important differential diagnosis is meningioma. Furthermore, the present case emphasizes the necessity of an intraoperative consultation and knowledge of this rare yet essential form of PCNSL so that appropriate studies can be ordered.</p>","PeriodicalId":45638,"journal":{"name":"Case Reports in Pathology","volume":null,"pages":null},"PeriodicalIF":0.7000,"publicationDate":"2021-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325585/pdf/","citationCount":"1","resultStr":"{\"title\":\"Primary Dural Lymphoma Mimicking En Plaque Cerebellopontine Angle Meningioma.\",\"authors\":\"Mei Xu,&nbsp;Ashish Bains,&nbsp;Yuan Rong\",\"doi\":\"10.1155/2021/2845995\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Primary dural lymphoma (PDL) usually arises from the calvarial dura without the brain parenchyma or systemic involvement and thus may not be considered as a typical form of primary CNS lymphoma (PCNSL). It is exceedingly rare. When it occurs, it might not be suspected as a primary diagnosis on clinical and radiologic findings. We present a PDL case that occurs at the cerebellopontine (CP) angle mimicking en plaque meningioma. The tumor histopathology showed a lymphoproliferative disorder immunophenotypically consistent with a low-grade marginal zone lymphoma. Bone marrow and systemic involvements were not identified, and a diagnosis of PDL was established. As a residual tumor at the CP angle was inaccessible to surgery, postoperative radiation therapy was performed. No recurrence was found at 15-month follow-up. PDLs are mostly indolent and have a good prognosis. There is no doubt that the most important differential diagnosis is meningioma. Furthermore, the present case emphasizes the necessity of an intraoperative consultation and knowledge of this rare yet essential form of PCNSL so that appropriate studies can be ordered.</p>\",\"PeriodicalId\":45638,\"journal\":{\"name\":\"Case Reports in Pathology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2021-07-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325585/pdf/\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Case Reports in Pathology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/2021/2845995\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2021/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"PATHOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Pathology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2021/2845995","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"PATHOLOGY","Score":null,"Total":0}
引用次数: 1

摘要

原发性硬脑膜淋巴瘤(PDL)通常起源于颅硬脑膜,没有脑实质或全身受累,因此可能不被认为是原发性中枢神经系统淋巴瘤(PCNSL)的典型形式。这是非常罕见的。当它发生时,它可能不会被怀疑为临床和放射学表现的初步诊断。我们提出了一个发生在桥小脑(CP)角的PDL病例,模拟斑块脑膜瘤。肿瘤组织病理学表现为淋巴增生性疾病,免疫表型与低级别边缘区淋巴瘤一致。骨髓和全身的累及没有被确定,PDL的诊断被确立。由于CP角处残留肿瘤无法手术,术后行放射治疗。随访15个月无复发。pdl多为无痛,预后良好。毫无疑问,最重要的鉴别诊断是脑膜瘤。此外,本病例强调术中咨询和了解这种罕见但必要的PCNSL形式的必要性,以便进行适当的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Primary Dural Lymphoma Mimicking En Plaque Cerebellopontine Angle Meningioma.

Primary Dural Lymphoma Mimicking En Plaque Cerebellopontine Angle Meningioma.

Primary Dural Lymphoma Mimicking En Plaque Cerebellopontine Angle Meningioma.

Primary Dural Lymphoma Mimicking En Plaque Cerebellopontine Angle Meningioma.

Primary dural lymphoma (PDL) usually arises from the calvarial dura without the brain parenchyma or systemic involvement and thus may not be considered as a typical form of primary CNS lymphoma (PCNSL). It is exceedingly rare. When it occurs, it might not be suspected as a primary diagnosis on clinical and radiologic findings. We present a PDL case that occurs at the cerebellopontine (CP) angle mimicking en plaque meningioma. The tumor histopathology showed a lymphoproliferative disorder immunophenotypically consistent with a low-grade marginal zone lymphoma. Bone marrow and systemic involvements were not identified, and a diagnosis of PDL was established. As a residual tumor at the CP angle was inaccessible to surgery, postoperative radiation therapy was performed. No recurrence was found at 15-month follow-up. PDLs are mostly indolent and have a good prognosis. There is no doubt that the most important differential diagnosis is meningioma. Furthermore, the present case emphasizes the necessity of an intraoperative consultation and knowledge of this rare yet essential form of PCNSL so that appropriate studies can be ordered.

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
20
审稿时长
12 weeks
×
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