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大脑胶质瘤病中的染色体

Chromosomes in gliomatosis cerebri.

作者信息

Hecht B K, Turc-Carel C, Chatel M, Lonjon M, Roche J L, Gioanni J, Hecht F, Gaudray P

机构信息

Laboratory of Molecular Genetics of Human Cancers, URA CNRS 1462, Nice, France.

出版信息

Genes Chromosomes Cancer. 1995 Oct;14(2):149-53. doi: 10.1002/gcc.2870140210.

Abstract

Gliomatosis cerebri is a rare brain tumor which histologically resembles a diffuse cerebral astrocytoma. It can simultaneously infiltrate multiple sites in the cerebrum, cerebellum, brainstem, and spinal cord. This remarkable diffuseness has led to the idea that gliomatosis cerebri does not derive from a solitary focus but must arise from a broad field of glial cells. We studied the chromosomes from gliomatosis cerebri in a 12-year-old boy by conventional cytogenetics and fluorescence in situ hybridization (FISH). Aside from normal cells, we found a majority of cells with the karyotype 44,XY,del(6)(q25),del(14)(q21), der(15;21)(q10;q10),add(18)(q22),del(19)(p12),add(20)(p13),-21. A smaller proportion of cells had 88 chromosomes with a doubling of this abnormal karyotype. These findings are consistent with a clonal neoplasm stemming from a single cell. The chromosome changes we observed, with the possible exception of the chromosome 6 deletion, did not resemble those frequently found in astrocytomas. Gliomatosis cerebri may therefore belong to a separate category of brain tumors.

摘要

大脑胶质瘤病是一种罕见的脑肿瘤,组织学上类似于弥漫性脑星形细胞瘤。它可同时浸润大脑、小脑、脑干和脊髓的多个部位。这种显著的弥漫性使人认为大脑胶质瘤病并非起源于单个病灶,而是必定源自广泛的胶质细胞区域。我们通过传统细胞遗传学和荧光原位杂交(FISH)技术研究了一名12岁男孩大脑胶质瘤病的染色体。除正常细胞外,我们发现大多数细胞的核型为44,XY,del(6)(q25),del(14)(q21), der(15;21)(q10;q10),add(18)(q22),del(19)(p12),add(20)(p13),-21。较小比例的细胞有88条染色体,是这种异常核型的双倍体。这些发现与源自单个细胞的克隆性肿瘤一致。我们观察到的染色体变化,可能6号染色体缺失除外,与星形细胞瘤中常见的变化不同。因此,大脑胶质瘤病可能属于脑肿瘤的一个独立类别。

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