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一名携带 K27M-H3.3 突变型毛细胞型星形细胞瘤的儿童的长期生存。

Long survival in a child with a mutated K27M-H3.3 pilocytic astrocytoma.

机构信息

Pediatric Oncology Unit, Oscar Lambret Center Lille, France.

Biochemistry and Molecular Biology Department, Lille University Hospital Lille, France.

出版信息

Ann Clin Transl Neurol. 2015 Apr;2(4):439-43. doi: 10.1002/acn3.184. Epub 2015 Mar 3.

Abstract

We report the first case of a child with a H3F3A K27M mutated pilocytic astrocytoma, who presented with a 10 years survival, and underwent spontaneous malignant transformation. The complex tumoral chromosomal rearrangements were consistent for genomic instability and for the histopathological features of malignant transformation into glioblastoma. H3F3A K27M mutations are rarely observed in benign neoplasms and may be associated with an adverse outcome. This mutation might not be the major driver that led to the onset of tumorigenesis, and we could consider that the associated TP53 mutation, would be required for malignant transformation.

摘要

我们报告了首例 H3F3A K27M 突变型毛细胞星形细胞瘤患儿,该患儿存活 10 年,并自发发生恶性转化。复杂的肿瘤染色体重排与基因组不稳定性和恶性转化为胶质母细胞瘤的组织病理学特征一致。H3F3A K27M 突变在良性肿瘤中很少见,可能与不良预后相关。这种突变可能不是导致肿瘤发生的主要驱动因素,我们可以认为,相关的 TP53 突变可能是恶性转化所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be5b/4402089/6671989b15d1/acn30002-0439-f1.jpg

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