成人弥漫性胶质瘤的瘤内组织学和分子异质性。

IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Clinical Neuropathology Pub Date : 2024-03-01 DOI:10.5414/NP301598
Trishhani Yogaretnam, Josephine Heffernan, Rosa Leung, Ciara Heeney, Andrea Walsh, Seamus Looby, John Caird, Francesca M Brett
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引用次数: 0

摘要

成人型弥漫性胶质瘤是最常见的成人恶性脑肿瘤。瘤内异质性会妨碍准确诊断和后续治疗。本病例报告记录了一名 29 岁女性左侧大脑半球的肿瘤,通过组织学和甲基化分析,该肿瘤具有瘤内异质性。她是在家中目睹全身强直阵挛发作后就诊的。两年前,她曾目睹过一次癫痫发作,但当时没有进行脑部成像检查。这次入院时,磁共振成像(MRI)显示左额叶有肿块病变,边缘不清,右侧中线偏移。左颞叶取样显示为 IDH 突变、ATRX 突变星形细胞瘤,增强的前部为 4 级,左颞叶为 2 级。甲基化分析证实了这种异质性。总之,从组织学和分子分析来看,这是一个肿瘤异质性的极好例子。从两年前的临床病史来看,该肿瘤很可能起源于低级别胶质瘤,随后发生了演变。
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Intratumoral histological and molecular heterogeneity in an adult diffuse glioma.

Adult-type diffuse gliomas are the most prevalent type of malignant adult brain tumors. Intratumoral heterogeneity can hinder accurate diagnosis and subsequent treatment. This case report documents a tumor with intratumoral heterogeneity, both histologically and by methylation analysis, located within the left cerebral hemisphere of a 29-year-old female. She presented after a witnessed generalized tonic clonic seizure at home. Two years prior she had a witnessed seizure; however, no brain imaging was done at the time. Magnetic resonance imaging (MRI), on this admission, showed a mass lesion in the left frontal operculum with poorly identified margins and right-sided midline shift. Sampling from the left temporal lobe showed an IDH-mutant, ATRX-mutant astrocytoma, which appeared grade 4 in the enhancing anterior portion and grade 2 in the left temporal lobe. Methylation analysis confirmed this heterogeneity. In summary, this is an excellent example of tumor heterogeneity both histologically and by molecular analysis. It is probable, given the clinical history of presentation 2 years prior, that this tumor originated as a low-grade glioma and subsequently evolved.

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来源期刊
Clinical Neuropathology
Clinical Neuropathology 医学-病理学
CiteScore
1.60
自引率
0.00%
发文量
70
审稿时长
>12 weeks
期刊介绍: Clinical Neuropathology appears bi-monthly and publishes reviews and editorials, original papers, short communications and reports on recent advances in the entire field of clinical neuropathology. Papers on experimental neuropathologic subjects are accepted if they bear a close relationship to human diseases. Correspondence (letters to the editors) and current information including book announcements will also be published.
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