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原发性胶质瘤与淋巴瘤并存:一例罕见病例报告

Co-existence of Primary Glioma and Lymphoma: An Unusual Case Report.

作者信息

Moritsubo Mayuko, Furuta Takuya, Natori Yoshihiro, Ohishi Yoshihiro, Sugita Yasuo, Miyoshi Hiroaki

机构信息

Department of Pathology, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Department of Neurosurgery, Aso Iizuka Hospital, Iizuka, Fukuoka, Japan.

出版信息

NMC Case Rep J. 2025 Aug 2;12:309-315. doi: 10.2176/jns-nmc.2024-0307. eCollection 2025.

Abstract

Composite or collision tumors in the central nervous system can significantly impact disease progression and metastasis, potentially affecting treatment efficacy. Studying the mechanisms associated with these tumors can provide neuro-oncologists with insights into tumor diversity, progression, and aid in the development of novel treatments. We encountered an 84-year-old female with memory disturbance who presented with tumors consistent with wild-type isocitrate dehydrogenase high-grade glioma and low-grade B-cell lymphoma at the same site. Magnetic resonance imaging revealed a solid enhanced mass in the right frontal lobe. A pre-operative suspicion of primary central nervous system lymphoma led to a brain biopsy. Histologically, 2 types of lesions were observed; the first consisted of atypical glial cells with diffuse infiltration and mitoses, positive for glial fibrillary acidic protein and negative for anti-isocitrate dehydrogenase 1 (IDH1)-R132H, characterized by partial amplification of and homozygous deletion of . The second type consisted of small atypical lymphoid positive forCD20, showing rearrangement, and minimal invasion of vessel walls while filling the perivascular space. Based on these findings, collision neoplasms of high-grade gliomas and marginal zone B-cell lymphomas were suspected. To our knowledge, this is the first reported co-existence of a glioma and intracranial lymphoma.

摘要

中枢神经系统的复合性或碰撞性肿瘤可显著影响疾病进展和转移,可能影响治疗效果。研究与这些肿瘤相关的机制可为神经肿瘤学家提供有关肿瘤多样性、进展的见解,并有助于开发新的治疗方法。我们遇到一名84岁有记忆障碍的女性,其同一部位出现了与野生型异柠檬酸脱氢酶高级别胶质瘤和低级别B细胞淋巴瘤相符的肿瘤。磁共振成像显示右额叶有一个实性强化肿块。术前怀疑为原发性中枢神经系统淋巴瘤,遂进行了脑活检。组织学上,观察到2种类型的病变;第一种由具有弥漫性浸润和有丝分裂的非典型胶质细胞组成,胶质纤维酸性蛋白呈阳性,抗异柠檬酸脱氢酶1(IDH1)-R132H呈阴性,其特征为 部分扩增和 纯合缺失。第二种类型由CD20呈阳性的小非典型淋巴细胞组成,显示 重排,血管壁侵犯轻微,同时填充血管周围间隙。基于这些发现,怀疑为高级别胶质瘤和边缘区B细胞淋巴瘤的碰撞性肿瘤。据我们所知,这是首次报道的胶质瘤与颅内淋巴瘤并存的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c20/12391670/605782b4925f/2188-4226-12-0309-g001.jpg

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