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具有毛细胞特征的高级别星形细胞瘤:病例报告及系统综述

High-grade astrocytoma with piloid features: case report and systematic review.

作者信息

Poluektov Yu M, Konovalov N A, Ryzhova M V, Bychkovskii N I, Lasunin N V, Zakirov B A, Kim D S

机构信息

Burdenko Neurosurgical Center, Moscow, Russia.

Sechenov First Moscow State Medical University, Moscow, Russia.

出版信息

Zh Vopr Neirokhir Im N N Burdenko. 2025;89(2):83-91. doi: 10.17116/neiro20258902183.

Abstract

UNLABELLED

In 2021, a new type of tumor was defined according to the new WHO classification (high-grade astrocytoma with piloid features HGAP). Morphological and neuroimaging differences of HGAP from pilocytic astrocytoma complicate diagnosis. Now, significant detection of this tumor is possible only using molecular genetic testing, in particular, methylation profile analysis.

OBJECTIVE

To present a patient with HGAP and perform a systematic review of studies devoted to adults with HGAP regarding clinical course, diagnosis, protocols and treatment outcomes.

MATERIAL AND METHODS

Selection of studies was carried out in accordance with the PRISMA recommendations. The authors analyzed the studies independently of each other. All data were systematized. A case report was described jointly with attending physicians and pathologists.

RESULTS AND DISCUSSION

HGAP is characterized by rapid progression and resistance to therapy. This case illustrates the importance of awareness of neurosurgeons and necessitates molecular genetic tests to identify this group of tumors.

CONCLUSION

HGAP is a rare and aggressive tumor. Treatment algorithm for such patients has not yet been developed. The world experience of treatment is presented by individual series. Analysis of methylation profile is necessary for patients with atypical course of tumors similar to pilocytic astrocytoma.

摘要

未标注

2021年,根据世界卫生组织新分类法定义了一种新型肿瘤(具有毛细胞样特征的高级别星形细胞瘤,HGAP)。HGAP与毛细胞型星形细胞瘤在形态学和神经影像学上的差异使诊断变得复杂。目前,只有通过分子遗传学检测,特别是甲基化谱分析,才能对这种肿瘤进行有效检测。

目的

介绍一例HGAP患者,并对有关成人HGAP的临床病程、诊断、方案和治疗结果的研究进行系统综述。

材料与方法

根据PRISMA建议进行研究筛选。作者们相互独立地分析研究。所有数据均进行了系统化整理。与主治医生和病理学家共同描述了一例病例报告。

结果与讨论

HGAP的特点是进展迅速且对治疗耐药。该病例说明了神经外科医生了解该病的重要性,并且需要进行分子遗传学检测来识别这组肿瘤。

结论

HGAP是一种罕见且侵袭性强的肿瘤。此类患者的治疗方案尚未制定。全球治疗经验以个别病例系列呈现。对于肿瘤病程不典型、类似毛细胞型星形细胞瘤的患者,分析甲基化谱是必要的。

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