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全面基因组分析在小儿型弥漫性高级别神经胶质瘤精准诊断中的应用。

Utility of Comprehensive Genomic Profiling for Precise Diagnosis of Pediatric-Type Diffuse High-Grade Glioma.

机构信息

Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.

Departments of Pediatrics, Okayama University Hospital.

出版信息

Acta Med Okayama. 2023 Jun;77(3):323-330. doi: 10.18926/AMO/65502.

Abstract

In the current World Health Organization classification of central nervous system tumors, comprehensive genetic and epigenetic analyses are considered essential for precise diagnosis. A 14-year-old male patient who presented with a cerebellar tumor was initially diagnosed with glioblastoma and treated with radiation and concomitant temozolomide chemotherapy after resection. During maintenance temozolomide therapy, a new contrast-enhanced lesion developed in the bottom of the cavity formed by the resection. A second surgery was performed, but the histological findings in specimens from the second surgery were different from those of the first surgery. Although genome-wide DNA methylation profiling was conducted using frozen tissue for a precise diagnosis, the proportion of tumor cells was insufficient and only normal cerebellum was observed. We then performed comprehensive genetic analysis using formalin-fixed paraffin-embedded sections, which revealed MYCN amplification without alteration of IDH1, IDH2, or Histone H3. Finally, the patient was diagnosed with pediatric-type diffuse high-grade glioma, H3-wildtype and IDH-wildtype. In conclusion, comprehensive genetic and epigenetic analysis should be considered in pediatric brain tumor cases.

摘要

在目前的世界卫生组织中枢神经系统肿瘤分类中,全面的遗传和表观遗传分析被认为是精确诊断所必需的。一名 14 岁男性患者因小脑肿瘤就诊,最初被诊断为胶质母细胞瘤,在切除后接受了放疗和替莫唑胺化疗的联合治疗。在维持替莫唑胺治疗期间,在切除形成的腔底部出现了新的增强对比病变。进行了第二次手术,但第二次手术标本的组织学发现与第一次手术不同。尽管使用冷冻组织进行了全基因组 DNA 甲基化分析以进行精确诊断,但肿瘤细胞的比例不足,仅观察到正常小脑。然后,我们使用福尔马林固定石蜡包埋切片进行了全面的基因分析,结果显示 MYCN 扩增而 IDH1、IDH2 或组蛋白 H3 没有改变。最终,该患者被诊断为小儿型弥漫性高级别神经胶质瘤,H3 野生型和 IDH 野生型。总之,对于小儿脑肿瘤病例应考虑进行全面的遗传和表观遗传分析。

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