原发性中枢神经系统弥漫性大 B 细胞淋巴瘤,伴有 MYC 和 BCL2 重排,与脑深部刺激装置有关。

IF 3.1 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2025-06-01 Epub Date: 2024-10-18 DOI:10.1007/s00428-024-03948-9
Kirill A Lyapichev, Sri Bharathi Kavuri, Patrick J Karas, Laura Wu, Nahyun Jo, John Heymann, Hadi Yaziji, Jianli Dong, Farkhod Tursunbaev, Rasha Alfattal, Michelle Madden Felicella
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引用次数: 0

摘要

原发性中枢神经系统弥漫性大b细胞淋巴瘤伴MYC和BCL2重排是一种非常罕见的淋巴瘤亚型。脑深部刺激是一种有效的微创治疗选择,用于治疗难治性运动障碍,以及一些精神疾病和慢性疼痛综合征。在此,我们报告一例中枢神经系统淋巴瘤,其周围发展的电极深部脑刺激(DBS)装置。一位患有耐药性特发性震颤的70岁女性在接下来的一年里接受了双侧丘脑DBS治疗,症状明显改善。她因反复震颤、视力模糊和意识不清而就诊于急诊科。成像显示以DBS电极为中心的4厘米非均匀增强。病理评估和系统检查证实原发性中枢神经系统弥漫性大b细胞淋巴瘤的诊断。鉴定出MYC和BCL2重排。据我们所知,这是首例报道的中枢神经系统淋巴瘤与DBS电极相关的病例。
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Primary central nervous system diffuse large B-cell lymphoma with MYC and BCL2 rearrangements associated with deep brain stimulation device.

Primary central nervous system (CNS) diffuse large B-cell lymphoma with MYC and BCL2 rearrangements is a very rare lymphoma subtype. Deep brain stimulation is an effective minimally invasive therapeutic option for the treatment of refractory movement disorders, as well as some psychiatric disorders and chronic pain syndromes. Herein, we report a case of CNS lymphoma, which developed around an electrode of a deep brain stimulation (DBS) device. A 70-year-old woman with drug-resistant essential tremor was treated with bilateral thalamic DBS with significant symptomatic improvement over the following year. She presented to the emergency department with recurrent tremor, blurred vision, and confusion. Imaging showed a 4 cm heterogeneously enhancing centered around the DBS electrode. Pathologic evaluation and systemic workup confirmed a diagnosis of primary CNS diffuse large B-cell lymphoma. MYC and BCL2 rearrangements were identified. To our knowledge, this is the first reported case of a CNS lymphoma associated with a DBS electrode.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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