Dysplastic gangliocytoma of the cerebellum with an unusual radiological finding.

Q4 Medicine
Ceskoslovenska patologie Pub Date : 2025-01-01
Markéta Hojsáková, Jana Engelová, Radim Brabec, Tereza Piskáčková, Marián Švajdler, Tomáš Klinger, Iva Dolinová, Renata Michalovská, Tomáš Jirásek
{"title":"Dysplastic gangliocytoma of the cerebellum with an unusual radiological finding.","authors":"Markéta Hojsáková, Jana Engelová, Radim Brabec, Tereza Piskáčková, Marián Švajdler, Tomáš Klinger, Iva Dolinová, Renata Michalovská, Tomáš Jirásek","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Dysplastic gangliocytoma of the cerebellum, also known as Lhermitte-Duclos disease (LDD), is a rare lesion of the posterior cranial fossa, classified among glioneuronal and neuronal tumors of the CNS, WHO grade 1. It typically has a characteristic radiological appearance on magnetic resonance imaging in the form of \"tiger stripes\" on T2-weighted images. In adults, LDD is often associated with Cowden syndrome and PTEN gene mutations. Our case report presents a 51-year-old patient with a somewhat atypical finding on magnetic resonance imaging, where histopathological examination surprisingly revealed dysplastic gangliocytoma of the cerebellum with a PTEN gene mutation, subsequently confirmed to be of germline origin. The patient was then examined for other manifestations of Cowden syndrome and is being followed up in a specialized clinic, with cascade genetic testing also conducted in her family.</p>","PeriodicalId":9861,"journal":{"name":"Ceskoslovenska patologie","volume":"61 2","pages":"92-97"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ceskoslovenska patologie","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Dysplastic gangliocytoma of the cerebellum, also known as Lhermitte-Duclos disease (LDD), is a rare lesion of the posterior cranial fossa, classified among glioneuronal and neuronal tumors of the CNS, WHO grade 1. It typically has a characteristic radiological appearance on magnetic resonance imaging in the form of "tiger stripes" on T2-weighted images. In adults, LDD is often associated with Cowden syndrome and PTEN gene mutations. Our case report presents a 51-year-old patient with a somewhat atypical finding on magnetic resonance imaging, where histopathological examination surprisingly revealed dysplastic gangliocytoma of the cerebellum with a PTEN gene mutation, subsequently confirmed to be of germline origin. The patient was then examined for other manifestations of Cowden syndrome and is being followed up in a specialized clinic, with cascade genetic testing also conducted in her family.

小脑发育不良神经节细胞瘤,影像学表现不寻常。
小脑发育不良神经节细胞瘤,也称为Lhermitte-Duclos病(LDD),是一种罕见的后颅窝病变,属于中枢神经系统的胶质神经元和神经元肿瘤,WHO分级为1级。它在磁共振成像上典型的放射学表现为t2加权图像上的“虎纹”。在成人中,LDD通常与考登综合征和PTEN基因突变有关。我们的病例报告提出了一位51岁的患者,在磁共振成像上有一些不典型的发现,组织病理学检查出人意料地显示小脑发育不良神经节细胞瘤伴PTEN基因突变,随后证实为种系起源。然后对患者进行了考登综合征的其他表现检查,并在一家专门诊所进行了随访,同时对其家庭进行了级联基因检测。
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
Ceskoslovenska patologie
Ceskoslovenska patologie Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
17
×
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:604180095
Book学术官方微信