Yu M Poluektov, N A Konovalov, M V Ryzhova, N I Bychkovskii, N V Lasunin, B A Zakirov, D S Kim
{"title":"【具有核样特征的高级别星形细胞瘤:病例报告及系统回顾】。","authors":"Yu M Poluektov, N A Konovalov, M V Ryzhova, N I Bychkovskii, N V Lasunin, B A Zakirov, D S Kim","doi":"10.17116/neiro20258902183","DOIUrl":null,"url":null,"abstract":"<p><p>In 2021, a new type of tumor was defined according to the new WHO classification (high-grade astrocytoma with piloid features<b>,</b> 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.</p><p><strong>Objective: </strong>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.</p><p><strong>Material and methods: </strong>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.</p><p><strong>Results and discussion: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":24032,"journal":{"name":"Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko","volume":"89 2","pages":"83-91"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[High-grade astrocytoma with piloid features: case report and systematic review].\",\"authors\":\"Yu M Poluektov, N A Konovalov, M V Ryzhova, N I Bychkovskii, N V Lasunin, B A Zakirov, D S Kim\",\"doi\":\"10.17116/neiro20258902183\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In 2021, a new type of tumor was defined according to the new WHO classification (high-grade astrocytoma with piloid features<b>,</b> 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.</p><p><strong>Objective: </strong>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.</p><p><strong>Material and methods: </strong>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.</p><p><strong>Results and discussion: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>\",\"PeriodicalId\":24032,\"journal\":{\"name\":\"Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko\",\"volume\":\"89 2\",\"pages\":\"83-91\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.17116/neiro20258902183\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17116/neiro20258902183","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
摘要
2021年,根据新的WHO分类定义了一种新的肿瘤类型(high-grade astrocytoma with piloid features, HGAP)。毛细胞星形细胞瘤HGAP的形态学和神经影像学差异使诊断复杂化。现在,只有通过分子基因检测,特别是甲基化谱分析,才能有效地检测出这种肿瘤。目的:介绍一名HGAP患者,并对成人HGAP患者的临床病程、诊断、治疗方案和治疗结果进行系统回顾。材料和方法:研究的选择按照PRISMA的建议进行。作者们各自独立地分析了这些研究。所有数据都被系统化了。病例报告与主治医师和病理学家共同描述。结果与讨论:HGAP的特点是进展迅速,对治疗有耐药性。这个病例说明了神经外科医生意识的重要性,需要分子基因测试来识别这组肿瘤。结论:HGAP是一种罕见的侵袭性肿瘤。目前还没有针对这类患者的治疗算法。世界治疗经验以个体系列呈现。对于类似毛细胞星形细胞瘤的非典型病程患者,分析甲基化谱是必要的。
[High-grade astrocytoma with piloid features: case report and systematic review].
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.
期刊介绍:
Scientific and practical peer-reviewed journal. This publication covers the theoretical, practical and organizational problems of modern neurosurgery, the latest advances in the treatment of various diseases of the central and peripheral nervous system. Founded in 1937. English version of the journal translates from Russian version since #1/2013.